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chzhbin

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209.86, 76.37, 49.45, 41.52, 39.05, 33.53, 30.87, 30.75, 28.73, 18.23, 17.02, 15.41, 15.23, 14.64, 11.19

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141.79, 134.09, 126.01, 112.15, 83.37, 78.19, 50.77, 47.25, 34.96, 33.19, 29.71, 27.10, 22.32, 21.86.

[ Last edited by chzhbin on 2012-5-10 at 13:05 ]
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chzhbin

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3Â¥: Originally posted by kaola0916 at 2012-05-10 19:26:16
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1 .     suberosol C
C15H24O     ÏàËÆ¶È:60%
Journal of ...

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1 .     (1S,4S,5S,6R,7S,10S)-dihydroxymaaliane
C15H26O2     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          2000          48(11)          77-80
Three New Sesquiterpenoid Glucosides of Ficus pumila Fruit
Junichi KITAJIMA,Kaoru KIMIZUKA,and Yasuko TANAKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

2 .     10¦Î-hydroxy-isocampheren-11-ene
C15H24O     ÏàËÆ¶È:66.6%
Phytochemistry          1999          50          1213-1218
Santalane and isocampherenane sesquiterpenoids from Illicium tsangii
Koon-Sin Ngo, Geo}rey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

3 .     Allo-aromadendrane-10 ¦Á,14-diol
C15H26O2     ÏàËÆ¶È:66.6%
Archives of Pharmacal Research          2008          31          21-27
A new sesquiterpene and other terpenoid constituents of Chisocheton penduliflorus
Jarinporn Phongmaykin, Takuya Kumamoto, Tsutomu Ishikawa, Rutt Suttisri and Ekarin Saifah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

4 .     (1S,10S)-9¦Á-hydroxy-allo-aromadendrane
C15H26O     ÏàËÆ¶È:60%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

5 .     (1R,10R)-9¦Â-hydroxyaromadendrane
C15H26O     ÏàËÆ¶È:60%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

6 .     (1R,10R)-aromadendran-9-one
C15H24O     ÏàËÆ¶È:60%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

7 .     (1R,10R)-13-hydroxyaromadendr-9-one
C15H24O2     ÏàËÆ¶È:60%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

8 .     2¦Â,9¦Â-dihydroxyaromadendr-1(10)-ene
C15H24O2     ÏàËÆ¶È:60%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

9 .     2¦Â,9¦Á-dihydroxyaromadendr-1(10)-ene
C15H24O2     ÏàËÆ¶È:60%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

10 .     compound 2a
C15H22O3     ÏàËÆ¶È:60%
Journal of Natural Products          2004          67          31-36
Africane-Type Sesquiterpenoids from the Argentine Liverwort Porella swartziana and Their Antibacterial Activity
Graciela Bovi Mitre, Norma Kamiya, Alicia Bardn, and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     maadiol
    ÏàËÆ¶È:60%
Phytochemistry          1992          31          3511-3514
Sesquiterpenoids and iridoid glycosides from Valeriana fauriei
Koichi Nishiya, Takefumi Kimura, Koichi Takeya, Hideji Itokawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

12 .     4¦Á,7¦Â-dihydroxy-10¦ÂH-guai-5-en-1¦Â,8¦Â-endoxide
C15H24O3     ÏàËÆ¶È:60%
Molecules          2011          16          518-522
A New Sesquiterpene with a Novel 1¦Â, 8¦Â-Oxygen Bridge from Heteropappus altaicus (willd.) Novopokr.
Yi-Feng Han, Xiao-Jing Gao and Hai Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

13 .     (1 S,13S,15S,28S)-2,12,14,14,29,29-Hexamethyl-18,25-dioxa-3,4,10,11-tetraazatricyclo[26.1.1.1(13,15)]hentriaconta-2,11-dien-5,9,19,24-tetrone
    ÏàËÆ¶È:56.2%
Chemistry of Natural Compounds          2011          Vol. 47, No. 2          210-214
SYNTHESIS FROM (+)-¦Á-PINENE OF OPTICALLY ACTIVE MACROCYCLES CONTAINING CYCLOBUTANE, ESTER,AZINE, OR HYDRAZIDE GROUPS
G. Yu. Ishmuratov,G. R. Mingaleeva, O. O. Shakhanova,R. R. Muslukhov, M. P. Yakovleva, L. P. Botsman,and A. G. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

14 .     (1S,13S,15S,28S)-2,12,14,14,29,29-hexamethyl-18,25-dioxa-3,4,10,11-tetraazatricyclo[26.1.1.1(13,15)]-hentriaconta-2,11-diene-5,9,19,24-tetraone
    ÏàËÆ¶È:56.2%
Russian Journal of Organic Chemistry          2011          47          1416-1425
Synthesis of macrocyclic azino and dihydrazido diesters by consecutive [2 + 1]- and [1 + 1]-condensations
G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva, O. O. Shakhanova and R. R. Muslukhov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     dendronobilin H
C15H26O3     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2007          Vol. 90          2386
Nine New Sesquiterpenes from Dendrobium nobile
Xue Zhanga)b)c), Hong-Wei Liud), Hao Gaoa)b)c), Hui-Ying Hane), Nai-Li Wangb)e), Hou-Ming Wuf), Xin-Sheng Yaoe), and Zhao Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     ent-4-epi-maaliol
C15H26O     ÏàËÆ¶È:53.3%
Phytochemistry          2005          66          599-609
Sesquiterpene constituents from the essential oil of the liverwort Plagiochila asplenioides
Adewale Martins Adio, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     (4S)-3¦Á,10¦Á,12,15-tetrahydroxycadinane
    ÏàËÆ¶È:53.3%
Phytochemistry          2002          59          479-488
Microbial transformation of cadina-4,10(15)-dien-3-one,aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740
Dwight O. Collins, Peter L.D. Ruddock, Jessica Chiverton de Grasse,William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     2¦Â-hydroxyaromadendr-1(10)-en-9-one
    ÏàËÆ¶È:53.3%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

19 .     (1S,10S)-1¦Á,2¦Â,9¦Â, 10btetrahydroxyaromadendrane
C15H26O4     ÏàËÆ¶È:53.3%
Phytochemistry          2002          60          475-481
Aromadendrane transformations by Curvularia lunata ATCC 12017
Dwight O. Collins, William F. Reynolds, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     [1RS,2RS,5E,9SR,10RS]-1,5,8,8-tetramethylbicyclo[8.1.0]undec-5-ene-2,9-diol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          1441-1442
A Stable Rearrangement Product of Humulene-4,5-epoxide
Raymond M. Carman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     1¦Â,7¦Á-dihydroxyeudesman-4(15)-ene
C15H26O2     ÏàËÆ¶È:53.3%
Planta Medica          2005          71          268-272
New Sesquiterpenes from Erigeron annus
Li, Xin; Yang, Min; Han, Yi-Feng; Gao, Kun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

22 .     compound 1
    ÏàËÆ¶È:53.3%
Phytochemistry          2000          55          749-753
The stereochemistry of ledol from Renealmia chrysotrycha: an NMR study
Maria Auxiliadora C. Kaplan, Helena R.L. Pugialli, Daise Lopes, Hugo E. Gottlieb
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

23 .     N-ethylisocarvomenthylamine
    ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          1980          16          397-402
SYNTHESIS AND STUDY OF THE STRUCTURE OF NEW N-SUBSTITUTED 2-METHYL-5-(1-METHYLETHYL)CYCLOHEXYLAMINES
I. I, Bardyshev, N. G. Kozlov, T. K. Vyalimyae, and T. I. Pekhk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

24 .     N-propylisocarvomenthylamine
    ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          1980          16          397-402
SYNTHESIS AND STUDY OF THE STRUCTURE OF NEW N-SUBSTITUTED 2-METHYL-5-(1-METHYLETHYL)CYCLOHEXYLAMINES
I. I, Bardyshev, N. G. Kozlov, T. K. Vyalimyae, and T. I. Pekhk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

25 .     8-oxo eremophila-6,9-dien-12-oic acid
    ÏàËÆ¶È:53.3%
Chinese Chemical Letters          1998          9          61-64
Eremophilane Sesquiterpenes from Cacalia Roborowskii
Suo Ming ZHANG,Gui Ling ZHAO,Rong LI and Guo Qiang LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

26 .     1¦Â,7¦Á-dihydroxyeudesma-4(15)-en
C15H26O2     ÏàËÆ¶È:53.3%
Chinese Chemical Letters          2005          16          61-63
New Eudesmenes from Erigeron annus
Xin LI, Qiu Hong WU, Kun GAO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

27 .     1,1,3,4,6-Pentamethyl-4a,5,6,7,8,8a-hexahydro-1H-isochromene
    ÏàËÆ¶È:53.3%
Molecules          2009          14          2780-2800
Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol®
Laura Chapado, Pablo J. Linares-Palomino, Concepci¨®n Bad¨ªa, Sof¨ªa Salido, Manuel Nogueras, Adolfo S¨¢nchez and Joaqu¨ªn Altarejos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

28 .     pterodontriol E
C15H28O3     ÏàËÆ¶È:53.3%
Journal of Asian Natural Products Research          2006          8          303-307
Two eudesmane sesquiterpenes from Laggera pterodonta
Y.-B. LIU, W. JIA, W.-Y. GAO, A.-H. ZHAO, Y.-W. ZHANG, Y. TAKAISHI and H.-Q. DUAN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

29 .     (-)-ledol
C15H26O     ÏàËÆ¶È:53.3%
Natural Product Research          2000          14          447-452
(-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry
Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

30 .     compound 1b
    ÏàËÆ¶È:53.3%
Natural Product Research          2000          14          447-452
(-)-Ledol from Calophyllum teysmanii: Structure and Stereochemistry
Shu-Geng Cao; Keng-Yeow Sim; S. H. Goh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

31 .     ¦Á-santal-11-ene-10-one
C15H22O     ÏàËÆ¶È:53.3%
Phytochemistry          1999          50          1213-1218
Santalane and isocampherenane sesquiterpenoids from Illicium tsangii
Koon-Sin Ngo, Geo}rey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

32 .     11-hydroxy-isocampheren-9-ene
    ÏàËÆ¶È:53.3%
Phytochemistry          1999          50          1213-1218
Santalane and isocampherenane sesquiterpenoids from Illicium tsangii
Koon-Sin Ngo, Geo}rey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

33 .     isocampheren-11-ene-10-one
C15H24O2     ÏàËÆ¶È:53.3%
Phytochemistry          1999          50          1213-1218
Santalane and isocampherenane sesquiterpenoids from Illicium tsangii
Koon-Sin Ngo, Geo}rey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

34 .     8-Oxo-eremophila-6,9-dien-12-oic acid
C15H20O3     ÏàËÆ¶È:53.3%
Phytochemistry          1998          48          519-524
Eremophilane sesquiterpenes from Cacalia roborowskii
Suoming Zhang, Guiling Zhao, Rong Li, Guoquiang Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

35 .     (¡À)-[1S-(1¦Â,4¦Â,4a¦Â,6¦Á,8a¦Á)]-1,6-Dimethyl-4-(1-methylethyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-1,6-naphthalenediol
    ÏàËÆ¶È:53.3%
Phytochemistry          1996          42          1097-1103
Three new oxygenated cadinanes from Baccharis species
Carmen L. Queiroga, Vera L. Ferracini, A. J. Marsaioli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

36 .     (11S)-5¦ÂH-eudesmane-3¦Á,13-diol
C15H28O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1994          Vol 57          1189
Synthetic Studies of Sesquiterpenes with a cis-Fused Decalin System, 4. Synthesis of (+)-5¦ÂH-Eudesma-3,11-diene, (-)-5¦ÂH-Eudesmane-4¦Â,11-diol, and (+)-5¦ÂH-Eudesmane-4¦Á,11-diol, and Structure Revision of a Natural Eudesmane-4,11-diol Isolated from Pluchea
Masayoshi Ando, Koji Arai, Kazuhira Kikuchi, Koji Isogai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

37 .     ptychanolide
    ÏàËÆ¶È:53.3%
Phytochemistry          1993          32          335-348
Terpenoids of the liverwort Frullanoides densifolia and Trocholejeunea sandvicensis
Motoo Tori, Hernita Arbiyanti, Zenei Taira, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

38 .     tamariscol
    ÏàËÆ¶È:53.3%
Phytochemistry          1991          30          2295-2300
Geographical distribution of tamariscol, a mossy odorous sesquiterpene alcohol, in the liverwort Frullania tamarisci and related species
Yoshinori Asakawa, Masakazu Sono, Mariko Wakamatsu, Keiko Kondo, Sinske Hattori, Masami Mizutani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

39 .     (1S,6S,8S,21S)-2,5,7,7,22,22-Hexamethyl-11,18-dioxa-3,4-diazatricyclo[19.1.1.1(6,8)]tetracosa-2,4-dien-12,17-dione
    ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2011          Vol. 47, No. 2          210-214
SYNTHESIS FROM (+)-¦Á-PINENE OF OPTICALLY ACTIVE MACROCYCLES CONTAINING CYCLOBUTANE, ESTER,AZINE, OR HYDRAZIDE GROUPS
G. Yu. Ishmuratov,G. R. Mingaleeva, O. O. Shakhanova,R. R. Muslukhov, M. P. Yakovleva, L. P. Botsman,and A. G. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

40 .     (2S,3R)-Diethyl-2-(cyclobutylmethyl)-3-hydroxy-2-methylsuccinate
C14H24O5     ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry          2011          19          2696-2706
Geminal dialkyl derivatives of N-substituted pantothenamides: Synthesis and antibacterial activity
T. Olukayode Akinnusi, Kenward Vong, Karine Auclair
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

41 .     Dihydro-¦Á-santaldiol
C15H26O2     ÏàËÆ¶È:53.3%
Phytochemistry          2012          77          304-311
¦Á-Santalol derivatives from Santalum album and their cytotoxic activities
Yukiko Matsuo ,Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

42 .     compound 2
    ÏàËÆ¶È:53.3%
Tetrahedron Letters          2000          41          2737-2740
Diastereodivergent synthesis of the C8¨CC18 precursor and C1¡ä¨CC11¡ä subunit of pamamycin 607 induced by a chiral sulfoxide group
Guy Solladi¨¦, Xavier J. Salom-Roig, Gilles Hanquet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

43 .     mandassidione
C15H22O2     ÏàËÆ¶È:53.3%
Phytochemistry          1988          27          3319-3321
Mandassidione and other sesquiterpenic ketones from Cyperus articulatus
B. Nyasse,R. Ghogomu,Tih B.L. Sondengam,M. T. Martin,B. Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

44 .     bis-(Dimethyldithiocarbamyl)thioethyl-¦Á-diethylphosphoryl- methane
C13H27N2O3PS5     ÏàËÆ¶È:53.3%
Journal of Heterocyclic Chemistry          2005          42          103-108
An approach to biologically important S-heterocycles,dithiocarbamyls,and their relevant phosphono derivatives
Maha D. Khidre,Azza A. Kamel and Wafaa M. Abdou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

45 .     ethyl 2-diazo-4-[(1R)-1,3,3-trimethyl-2-methylenecyclohexyl]-3-oxobutanoate
    ÏàËÆ¶È:53.3%
Indian Journal of Chemistry          2009          48B          413-422
Enantiospecific total synthesis of ent-10,11-thapsan-10-ol
Srikrishna,A; Anebouselvy,K
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

46 .     Compound 14
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chmesitry          2003          41          1034-1037
Complete NMR assignment of (+)-10¦Â, 14-dihydroxy-allo-aromadendrane
Lucin¨¦ia Vizzotto, Rozanna Marques Muzzi and D¨ºnis Pires de Lima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

47 .     Dihydro-¦Á-santalen-12-one
C15H24O     ÏàËÆ¶È:53.3%
Phytochemistry          1984          23          595-597
Sesquiterpenes from severinia buxifolia
Wu Tian-Shung, Masatake Niwa, Hiroshi Furukawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

48 .     compound 4
    ÏàËÆ¶È:53.3%
Phytochemistry          1984          23          1647-1649
Oxidized aristolane sesquiterpenes from Aristolochia debilis
Gerhard R¨¹cker, Ralf Mayer, Eberhard Breitmaier, Georg Will, Armin Kirfel, Mohamed El Kordy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     Terebinthene
    ÏàËÆ¶È:53.3%
Phytochemistry          2010          71          1371-1374
Spirocyclopropane-type sesquiterpene hydrocarbons from Schinus terebinthifolius Raddi
Rita Richter, Stephan H. von Reuß, Wilfried A. König
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     ptychanolide
C15H22O3     ÏàËÆ¶È:53.3%
Tetrahedron letters          1981          22          5307-5310
Ptychanolide, a sesquiterpenoid with a new type skeleton from the liverwort ptychanthus striatus (lehm. et lindenb.) nees
Reiji Takeda, Hideo Naoki, Takashi Iwashita, Yoshio Hirose
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

51 .     1¦Â,5¦Á-dihydroxy-11¦ÁH-eudesma-4(15)-en-12,8¦Â-olide
C15H22O4     ÏàËÆ¶È:53.3%
Tetrahedron          2010          66          9379-9388
New sesquiterpenes from Inula japonica Thunb. with their inhibitory activities against LPS-induced NO production in RAW264.7 macrophages
Jiang-Jiang Qin, Hui-Zi Jin, Jia-Xian Zhu, Jian-Jun Fu, Qi Zeng, Xiang-Rong Cheng, Yan Zhu, Lei Shan, Shou-De Zhang, Yue-Xing Pan, Wei-Dong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

52 .     (-)-10(R)-hydroxyalloaromadendrane
C15H26O     ÏàËÆ¶È:53.3%
Tetrahedron          1996          52          2359-2368
Terpenoids with antifouling activity against barnacle larvae from the marine sponge Acanthella cavernosa
Hiroshi Hirota, Yasuhiko Tomono, Nobuhiro Fusetani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

53 .     (4S,2'S,3'S)-3-(3'-azido-2'-methylpentyl)-4-isopropyl-2-oxazolidinone
C13H22N2O3     ÏàËÆ¶È:53.3%
The Journal of Organic Chemistry          2002          67          1760-1767
Kulokekahilide-1, a Cytotoxic Depsipeptide from the Cephalaspidean Mollusk Philinopsis speciosa
Junji Kimura, Yuuki Takada, Tomoko Inayoshi, Yoichi Nakao, Gilles Goetz, Wesley Y. Yoshida, and Paul J. Scheuer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

54 .     9¦Â-hydroxy-6,7¦ÁH,11¦ÂH-eudesm-4-en-6,12-olide
    ÏàËÆ¶È:53.3%
Tetrahedron          1995          51          5609-5616
Synthesis of 9-oxyfunctionalized eudesmanes from artemisin
Victoria Bargues, Gonzalo Blay, Begoña Garc¨ªa, Cristina L. Garc¨ªa, Jos¨¦R. Pedro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

55 .     allohimachalol
C15H26O     ÏàËÆ¶È:53.3%
Tetrahedron          1999          55          759-770
Allohimachalane, seco-allohimachalane and himachalane sesquiterpenes from Illicium tsangii
Koon-Sin Ngo, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

56 .     (1S,6S,8S,21S)-2,5,7,7,22,22-hexamethyl-11,18-dioxa-3,4-diazatricyclo[19.1.1.1(6,8)]tetracosa-2,4-diene-12,17-dione
    ÏàËÆ¶È:53.3%
Russian Journal of Organic Chemistry          2011          47          1416-1425
Synthesis of macrocyclic azino and dihydrazido diesters by consecutive [2 + 1]- and [1 + 1]-condensations
G. Yu. Ishmuratov, G. R. Mingaleeva, M. P. Yakovleva, O. O. Shakhanova and R. R. Muslukhov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

57 .     peribysin F
C15H26O4     ÏàËÆ¶È:53.3%
The Journal of Antibiotics          2005          58          185-191
Absolute Stereostructures of Cell-adhesion Inhibitors, Peribysins A, E, F and G, Produced by a Sea Hare-derived Periconia sp. FREE
Takeshi Yamada, Mitsunobu Doi, Atsuko Miura, Waka Harada, Mika Hiramura, Katsuhiko Minoura, Reiko Tanaka and Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

58 .     6¦Â-Hydroxypathoulol
C15H26O2     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2011          94          218-223
New Patchoulol-Type Sesquiterpenoids from Pogostemon cablin
Lei Zhou, Min Xu, Chong-Ren Yang, Yi-Fei Wang and Ying-Jun Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

59 .     compound 2a
    ÏàËÆ¶È:52.9%
Chemical & Pharmaceutical Bulletin          2006          54          1370-1379
Studies on Nepalese Crude Drugs. XXIX. Chemical Constituents of Dronapuspi, the Whole Herb of Leucas cephalotes SPRENG.
Yukinori Miyaichi, Akiko Segawa and Tsuyoshi Tomimori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

60 .     Stanozolol
    ÏàËÆ¶È:52.9%
Steroids          1992          57          537-550
17-Epimerization of 17¦Á-methyl anabolic steroids in humans: metabolism and synthesis of 17¦Á-hydroxy-17¦Â-methyl steroids
Willi Schänzer, Georg Opfermann, Manfred Donike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

61 .     3¦Á,4¦Á-dihydroxyclerodan-15-oic acid
C20H36O4     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2003          Vol. 86          3187
Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana
Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

62 .     3¦Á,4¦Á-dihydroxyclerodan-15-oic acid
C20H36O4     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2003          Vol. 86          3187
Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana
Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

63 .     ketone
C18H30O     ÏàËÆ¶È:50%
Journal of Natural Products          1997          60          1261-1264
Cyclic Peroxides and Related Norterpenes from a Southern Australian Marine Sponge, Mycale sp.
Robert J. Capon, Simone J. Rochfort, and Simon P. B. Ovenden
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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64 .     [(1aR,3aR,4S,5R,7aR,7bS)-Decahydro-4,5,7¦Á,7¦Â-tetramethylnaphtho[1,2-b]oxiren-4-yl]acetaldehyde
C16H26O2     ÏàËÆ¶È:50%
Chemistry & Biodiversity          2009          6          447-458
Structure¨C Activity Relationship Studies on the Mosquito Toxicity and Biting Deterrency of Callicarpenal Derivatives
Charles L. Cantrell, Jerome A. Klun, Julia Pridgeon, James Becnel, Solomon Green III, and Frank R. Fronczek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

65 .     5,6¦Á-cyclopropano-5¦Á-androst-7-ene-3,17-dione
C20H26O2     ÏàËÆ¶È:50%
Steroids          2000          65          863-870
Microbial transformation of 3-hydroxy-5,6-cyclopropanocholestanes - An alternative route to 6-methylsteroids
Jiann-Long Yan, Shoei-Sheng Lee, K. C. Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

66 .     compound 2c
    ÏàËÆ¶È:50%
Journal of Natural Products          1984          Vol 47          592-599
Cmr Spectroscopy of Labdanic Diterpenes and Related Substances
Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

67 .     compound 19a
    ÏàËÆ¶È:50%
Journal of Natural Products          1984          Vol 47          592-599
Cmr Spectroscopy of Labdanic Diterpenes and Related Substances
Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

68 .     16-(furan-2-ylmethylene)-5¦Á-androstan-3,17-dione
C24H30O3     ÏàËÆ¶È:50%
Steroids          2011          76          709-723
Synthesis, characterization and biological evaluation of some 16E-arylidene androstane derivatives as potential anticancer agents
Hao Guo, Haotian Wu, Jin Yang, Yuling Xiao, Hans-Josef Altenbach, Guofu Qiu,Hao Hu, Zhongyuan Wu, Xianran He, Dingshan Zhou, Xianming Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

69 .     lagaspholone A
C20H28O3     ÏàËÆ¶È:50%
Organic Letters          2007          Vol. 9, No. 3          489-492
Lagaspholones A and B: Two New Jatropholane-Type Diterpenes from Euphorbia lagascae
No¨¦lia Duarte and Maria-Jos¨¦ U. Ferreira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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70 .     ¦Â-himachalene
C16H24Cl2O3     ÏàËÆ¶È:50%
Zeitschrift f¨¹r Naturforschung B          2004          59b          1177-1179
Synthesis, Structure, and Absolute Configuration of a New Cyclopropanic Compound Derived from the Sesquiterpene ¦Â-Himachalene
Hossni Ziyat, Soufiane El Houssame, Mustapha Ait Ali, My Youssef Ait Itto, Abdellah Karim, RudolfWartchow, and Holger Butenschön
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

71 .     (4R,8R,9R)-8-methoxyisocaryolane-9,15-diol
C16H28O3     ÏàËÆ¶È:50%
Journal of Natural Products          2011          74          1707-1712
Biotransformation of Bioactive Isocaryolanes by Botrytis cinerea
Jociani Ascari, Maria Am elia Diamantino Boaventura, Jacqueline Aparecida Takahashi, Rosa Dur an-Patr on, Rosario Hern andez-Gal an, Antonio J. Mac¨ªas-S anchez, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

72 .     compound 9
    ÏàËÆ¶È:50%
Tetrahedron Letters          2000          41          5669-5672
Total synthesis of (¡À)-nakamurol-A and its 13-epimer: tentative assignment of the C-13 relative configuration
Josep Bonjoch, Javier Cuesta, Sandra D¨ªaz, Asensio Gonz¨¢lez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

73 .     compound 25
    ÏàËÆ¶È:50%
Tetrahedron Letters          2000          41          6643-6647
An enantiospecific approach to thapsanes from R-carvone: synthesis of (−-thaps-8-en-5-ol
A. Srikrishna, K. Anebouselvy, T. Jagadeeshwar Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

74 .     (1R,3S,6R,7R)-7-(tert-butyldimethylsilyloxy)-3,6,10,10-tetramethyltricyclo[4.4.0.01,3]decan-4-one
C20H36O2Si     ÏàËÆ¶È:50%
Indian Journal of Chemistry          2008          47B          449-459
Enantiospecific synthesis of thaps-8-en-5-ol via stereospecific
Srikrishna,A; Anebouselvy,K
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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75 .     cis-3-(2-Undecylcyclopropyl)propionic acid
C17H32O3     ÏàËÆ¶È:50%
Molecules          2011          16          9972-9982
Isolation of C11 Compounds and a Cyclopropane Fatty Acid from an Okinawan Ascidian, Diplosoma sp.
Tamanna Rob, Takayuki Ogi, Wilmar Maarisit, Junsei Taira and Katsuhiro Ueda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

76 .     isothiocyanate 1
    ÏàËÆ¶È:50%
Natural Product Research and Development          2003          15          199-202
STUDIES ON THE CHEMICAL CONSTITUENTS OF MARINE SPONGE ACANTHELLASP.FROM THE SOUTH CHINA SEA
YAN Xiao-hong; SONG Guo-qiang; ZHOU Xiu-hong; LIU Song-bai; GUO Yue-wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1 .     suberosol C
C15H24O     ÏàËÆ¶È:60%
Journal of Natural Products          2002          65          887-891
Suberosols A-D, Four New Sesquiterpenes with ¦Â-Caryophyllene Skeletons from a Taiwanese Gorgonian Coral Subergorgia suberosa
Guey-Horng Wang, Atallah F. Ahmed, Jyh-Horng Sheu, Chang-Yih Duh, Ya-Ching Shen, and Li-Tang Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 11
    ÏàËÆ¶È:58.8%
Tetrahedron          1991          47          9411-9418
New examples of acyclic and cyclic C-15 acetogenins from laurencia pinnatifida. Reassignment of the absolute configuration for E and Z pinnatifidienyne.
Manuel Noite, Antonio G. Gonzalez, Fernando Cataldo, Mat¨ªas L. Rodr¨ªguez, Ivan Brito
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     3,3,6,6-Tetramethyl-9-(2-nitrophenyl)-3,4,6,7-tetrahydroacridine-1,8(2H,5H,9H,10H)-dione
C23H26N2O4     ÏàËÆ¶È:57.1%
Molecules          2009          14          1468-1474
An Efficient One-Pot Three-Component Synthesis of Fused 1, 4-Dihydropyridines Using HY-Zeolit
Mohammad Nikpassand, Manouchehr Mamaghani and Khalil Tabatabaeian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     compound 5
C15H22O2     ÏàËÆ¶È:57.1%
Chemical Journal of Chinese Universities          2009          30          1329-1331
First Asymmetric Synthesis of (7R, 10S)-Boivinianin B
XU Bo-Yan, SONG Na, LIWen-Ze, XIN Zhi-Jun, LIYing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     5-Cyanotetralin
C11H11N     ÏàËÆ¶È:57.1%
Canadian Journal of Chemistry          2006          84          10-20
Steric effects in the phototransposition reactions of dialkylbenzenes
C.M. Gonzalez and J.A. Pincock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     1-Methyl-2-{[(1R,2S,5R)-6,6-dimethylbicyclo[3.1.1]heptyl-2]methylsulfonyl}-1H-imidazole
C14H22N2O2S     ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          2012          48          38-42
SYNTHESIS OF NEW MONOTERPENE SULFONYLIMIDAZOLES
M. Ya. Demakova,D. V. Sudarikov,S. A. Rubtsova,L. L. Frolova,and A. V. Kuchin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Methyl (1R*,2R*,10 R*)-1,10-Dimethyl-7-oxo-bicyclo[4.4.0]dec-5-ene-2-carboxylate
C14H20O3     ÏàËÆ¶È:57.1%
Journal of the Chemical Society, Perkin Transactions 1          1991                   1919-1922
Total synthesis of kanshone A, a sesquiterpene isolated from Nardostachys chinensis (Valerianaceae)
Motoo Tori, Hirosuke Furuta and Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     3,3,6,6-Tetramethyl-9-(2-nitrophenyl)-3,4,6,7,9,10-hexahydroacridine-1,8(2H,5H)-dione
C23H26N2O4     ÏàËÆ¶È:57.1%
Chinese Chemical Letters          2011          22          531-534
Multicomponent synthesis of dihydropyridines catalyzed by l-proline
Leila Zare, Mohammad Nikpassand
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     1-Methyl-2-[((1S,2S,5R)-2-isopropyl-5-methylcyclohexyl)sulfanyl]-1H-imidazole
C14H24N2S     ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          2012          47          899-902
Synthesis of neomenthylsulfanylimidazoles
M. Ya. Demakova, D. V. Sudarikov, S. A. Rubtsova, P. A. Slepukhin and A. V. Kuchin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (2R,5R,10S)-2-N-methyl-6-axene
C16H29N     ÏàËÆ¶È:56.2%
Tetrahedron          2006          62          10393-10399
Stereochemical challenges in characterizing nitrogenous spiro-axane sesquiterpenes from the Indo-Pacific sponges Amorphinopsis and Axinyssa
Christopher J. Wegerski, Rachel N. Sonnenschein, Freddy Cabriales, Frederick A. Valeriote, Teatulohi Matainaho, Phillip Crews
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (3e,5e)-3,7,11-trimethyl-9-oxododeca-1,3,5-triene
C15H24O     ÏàËÆ¶È:53.3%
Journal of Natural Products          2001          64          401-405
New Acyclic Sesquiterpenes and Norsesquiterpenes from the Caribbean Gorgonian Plexaurella grisea
Ana Rueda, Eva Zub¨ªa, Mar¨ªa J. Ortega, and Javier Salv¨¢
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     9¦Á,15-dihydroxyafricanane
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          1019-1021
New Oxygenated Africanenes from the Soft Coral Sinularia dissecta
P. Ramesh, N. Srinivasa Reddy, T. P. Rao, and Y. Venkateswarlu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     clovan-2¦Á,9¦Â-diol
C16H28O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1998          61          1348-1351
The Biotransformation of Some Clovanes by Botrytis cinerea
Isidro G. Collado, James R. Hanson, Antonio J. Mac¨ªas-S¨¢nchez, and D. Mobbs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

14 .     3,10-Epoxygermacr-4(14)-en-8-one
C15H24O2     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          1991          27          20-24
NEW TERPENOIDS OF THE ESSENTIAL OIL OF LEDUM PALUSTRE
N. I. Belousova, A. V. Tkachev,M. M. Shakirov, and V. A. Khan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     cytotoxic sesquiterpene caryol-7-en-6-ol
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2009          92          375-378
A New Tricyclo[6.3.1.02,5]dodecane Sesquiterpene from Cultures of the Basidiomycete Campanella junghuhnii
Rong Liu, Zhong-Yu Zhou, Di Xu, Fei Wang, Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

16 .     ( 1R*,4R*,5Z,9S*)-5-isopropyl-3,3,9-trimethylbicyclo[4. 3.0]nona-5-en-4-ol
C15H26O     ÏàËÆ¶È:53.3%
Journal of Natural Products          1991          Vol 54          1025
New Sesquiterpenes and C15 Acetogenins from the Marine Red Alga Laurencia implicata
Anthony D. Wright, Gabriele M. König, Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     4-hydroxy-5-brasilene
C15H26O     ÏàËÆ¶È:53.3%
Phytochemistry          1991          30          1921-1927
Brasilane-type sesquiterpenoids from the mediterranean red alga Laurencia obtusa
Vincenzo Amico, Salvatore Caccamese, Placido Neri, Giusy Russo, Mario Foti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

18 .     isodauc-7(14)-en-6¦Á,10¦Â-diol
C15H26O2     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2010          58          991-994
Sesquiterpenoids and Other Constituents from Senecio argunensis
Wei-Dong Xie, Yu-Fang Niu, Peng-Xiang Lai and Kyung-Ho Row
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     2-chloro-3-hydroxy-¦Á-chamigren-9-one
C15H23ClO2     ÏàËÆ¶È:53.3%
Phytochemistry          1987          26          1053-1057
Chamigrane metabolites from a Jamaican variety of laurencia obtusa
Mary R. Brennan,Karen L. Erickson,Donna A. Minott,Keith O. Pascoe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     compound 12aii
C15H17NOS     ÏàËÆ¶È:53.3%
Journal of Heterocyclic Chemistry          2005          42          201-207
Intramolecular photoreactions of thiohomophthalimides with an alkenyl group in their N-Side chain. Regioselective synthesis of heterocycle-fused isoquinoline derivatives through [2+2] photocycloaddition
Haruko Takechi,Hajime Takahashi and Minoru Machida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     compound 5d
C15H24O2     ÏàËÆ¶È:53.3%
Tetrahedron Letters          2005          46          5803-5806
TiF4-mediated biomimetic alkylation-cyclization cascade reaction of 2-trimethylsilylmethyl-1,5-dienes with aldehydes
Luigi Anastasia, Elios Giannini, Giuseppe Zanoni, Giovanni Vidari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

22 .     compound 4a
C15H24O2     ÏàËÆ¶È:53.3%
Tetrahedron          1999          55          9117-9132
New acorane- and cuparane-type sesqui- and new labdane- and seco-labdanne-type diterpenoids from the Japanese liverwort Jungermannia infusca (Mitt.) Steph.
Fumihiro Nagashima, Makoto Suzuki, Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

23 .     (9R,9aS)-5,5,9-trimethyl-5,6,7,8,9,9a-hexahydro-1H-benzo[7]annulene-3-carbaldehyde
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2011          74          585-595
Male-Specific Sesquiterpenes from Phyllotreta Flea Beetles
Robert J. Bartelt, Bruce W. Zilkowski, Allard A. Coss¨¦, Udo Schnupf, Karl Vermillion, and Frank A. Momany
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

24 .     2-{[(1R,2S,5R)-6,6-Dimethylbicyclo[3.1.1]heptyl-2]methylsulfonyl}-1H-benzimidazole
C17H22N2O2S     ÏàËÆ¶È:52.9%
Chemistry of Natural Compounds          2012          48          38-42
SYNTHESIS OF NEW MONOTERPENE SULFONYLIMIDAZOLES
M. Ya. Demakova,D. V. Sudarikov,S. A. Rubtsova,L. L. Frolova,and A. V. Kuchin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

25 .     (3R,6R)-6-(2-bromo-5-methoxymethoxy-4-methyl)phenyl-2-methylheptane-2,3-diol
C17H27O4Br     ÏàËÆ¶È:52.9%
Heterocycles          2003          61          125-131
Enantiocontrolled Total Synthesis of (+)-Heliannuol D via Palladium-mediated Heterocyclization
Hidetoshi Kishuku, Tomoyuki Yoshimura, Toshiyuki Kakehashi, Mitsuru Shindo, and Kozo Shishido*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

26 .     compound 12
    ÏàËÆ¶È:52.9%
Tetrahedron          1991          47          9411-9418
New examples of acyclic and cyclic C-15 acetogenins from laurencia pinnatifida. Reassignment of the absolute configuration for E and Z pinnatifidienyne.
Manuel Noite, Antonio G. Gonzalez, Fernando Cataldo, Mat¨ªas L. Rodr¨ªguez, Ivan Brito
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

27 .     2-acetyl-3a¦Â-methyl-3a,6,7,7a¦Â-tetrahydro-1H-inden-4-oic acid methyl ester.
C14H18O3     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          241-245
Eremophilane-Type Sesquiterpene Derivatives from the Roots of Ligularia lapathifolia
Dong-Qing Fei, Shi-Gang Li, Chun-Mei Liu, Gang Wu, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

28 .     20R-3¦Â-[(6-deoxy-¦Á-L-mannopyranosyl)oxy]-14¦Â-hydroxybufa-4-enolide
C30H46O8     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1987          35          1839-1846
Studies on Cardiac Ingredients of Plants. III. Structural Confirmation and Biological Activity of Reduced Proscillaridins
JUN MORI,SHIN-ICHI NAGAI,JINSAKU SAKAKIBARA,KAZUMI TAKEYA,YOSHIHIRO HOTTA and HIROAKI ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

29 .     (5R,6S,9R)-6-Isopropyl-9-methyl-1-oxo-4-thiaspiro[4.5]-decane
C12H22SO     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2008          44          728-731
OXIDATION OF MENTHONE OXOTHIOLANE
A. V. Timshina, S. A. Rubtsova, I. N. Alekseev, M. I. Kodess,E. G. Mamochkina, P. A. Slepukhin, and A. V. Kuchin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

30 .     (4R,5R,6S,9R)-6-Isopropyl-9-methyl-1-oxo-4-thiaspiro[4.5]-decane-4-sulfoxide
C12H22SO2     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2008          44          728-731
OXIDATION OF MENTHONE OXOTHIOLANE
A. V. Timshina, S. A. Rubtsova, I. N. Alekseev, M. I. Kodess,E. G. Mamochkina, P. A. Slepukhin, and A. V. Kuchin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

31 .     Hexadeca-10E,12Z-dien-1-ol
    ÏàËÆ¶È:50%
Chemistry of Natural Compounds          1993          29          668-673
INSECT PHEROMONES AND THEIR ANALOGUES XLVIII. A CONVENIENT SYNTHESIS OF THE 10E,12Z- AND 10E,12E- ISOMERS OF HEXADECADIEN-1-OL AND OF HEXADECA-10E,12Z-DIENAL -- COMPONENTS OF THE SEX PHEROMONE OF THE SILKWORM MOTH
V. N. Odinokov, G. Yu. Ishmuratov, I. M. Ladenkova,O. V. Sokol'skaya, R. R. Muslukhov, V. R. Akhmetova,E. V. Gorobets, A. V. Kuchin, and G. A. Tolstikov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

32 .     ¦Á¨C(2-Cyclopenten-1-yl)-4-methylbenzenemethanol
C13H16O     ÏàËÆ¶È:50%
Molecules          2001          6          655-662
Use of Cyclic Allylic Bromides in the Zinc¨CMediated Aqueous Barbier¨CGrignard Reaction
Gary W. Breton, John H. Shugart, Christine A. Hughey, Brian P. Conrad and Suzanne M. Perala
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

33 .     2¦Â−acetoxy-8¦Â,12-epoxy-13,14,15,16-tetranor-ent-labdan-17-ol
    ÏàËÆ¶È:50%
Molecules          2007          12          2605-2620
Oxidative Degradations of the Side Chain of Unsaturated Ent-labdanes. Part II
Luis E. Catal¨¢n, Karen C. Mar¨ªn, H¨¦ctor C. Altamirano, Mauricio C. Fritis and Mar¨ªa C. Chamy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

34 .     compoun 9
    ÏàËÆ¶È:50%
Natural Product Research          1993          2          129-135
Preparation of a Monochiral Terpenoid SynthonfFrom Carvone Using a Stereoselective Intramolecular Nitrile Oxide Cycloaddition
J. -P. Gesson; S. A. M. Nieuwenhuis; B. Renoux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

35 .     (2S,2aR,6S,7aS,7bS,8R,9S)-7b-butylhexahydro-9-methyl-4H-2,2,6-(epoxy[1]propanyl[3]ylidene)furo[2,3,4-gh]pyrrolizin-10-one
C16H23NO6     ÏàËÆ¶È:50%
Journal of Natural Products          2010          73          935-941
Semisynthesis and Acetylcholinesterase Inhibitory Activity of Stemofoline Alkaloids and Analogues
Kwankamol Sastraruji, Thanapat Sastraruji, Stephen G. Pyne, Alison T. Ung, Araya Jatisatienr and Wilford Lie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

36 .     pectinolide C
C14H20O5     ÏàËÆ¶È:50%
Journal of Natural Products          1993          Vol 56          583
Structure and Stereochemistry of Pectinolides A-C, Novel Antimicrobial and Cytotoxic 5,6-Dihydro-¦Á-pyrones from Hyptis pectinata
Rogelio Pereda-Miranda, Lourdes Hern¨¢ndez, Manuela Judith Villavicencio, Miriam Novelo, Patricia Ibarra, Heebyung Chai, John M. Pezzuto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

37 .     10,12-peroxycalamenene
C15H20O2     ÏàËÆ¶È:50%
Phytochemistry          1995          40          125-128
Antimalarial sesquiterpenes from tubers of Cyperus rotundus: structure of 10, 12-Peroxycalamenene, a sesquiterpene endoperoxide
C. Thebtaranonth, Y. Thebtaranonth, S. Wanauppathamkul, Y. Yuthavong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

38 .     Methyl omphalate
    ÏàËÆ¶È:50%
Phytochemistry          1995          38          651-653
Sesquiterpenes and a phenolic compound from the liverwort Omphalanthus filiformis
Motoo Tori, Katsuyuki Nakashima, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

39 .     methyl 4-(2-hydroxy-1,5-dimethyl-3-oxohexyl)-1-cyclo-hexene-1-carboxylate
C16H26O4     ÏàËÆ¶È:50%
Phytochemistry          1993          32          1163-1165
Juvabione analogues from two Abies sachalinensis trees
Kenzo Kawai, Chika Takahashi, Tamie Takada, Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

40 .     4,8,8-trimethyl-4-acetylcyclloctanon
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          1976          59          1-13
Die Thermolyse von 2,2,6,7-Tetramethyl-1,7-epidioxybicyclo[4.3.O]non-8-en
von Werner Skorianetz und Gunther Ohloff
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

41 .     (1R,4R,4aS,8aS)-1,2,3,4,4a,7,8,8a-Octahydro-4-isopropyl-6-methylnaphthalen-1-ol
C14H24O     ÏàËÆ¶È:50%
Organic Letters          2010          Vol.12,No.5          904-907
Total Synthesis of 10-Isocyano-4-cadinene and Determination of Its Absolute Configuration
Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata,Erina Yoshimura, Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

42 .     (1R,4R,4aS,8aS)-4-isopropyl-6-methyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-ol
C14H24O     ÏàËÆ¶È:50%
The Journal of Organic Chemistry          2011          76          6558-6573
Total Synthesis of 10-Isocyano-4-cadinene and Its Stereoisomers and Evaluations of Antifouling Activities
Keisuke Nishikawa, Hiroshi Nakahara, Yousuke Shirokura, Yasuyuki Nogata, Erina Yoshimura,Taiki Umezawa, Tatsufumi Okino, and Fuyuhiko Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

43 .     2,3,4,4a,5,6-hexahydro-7-methyl-pyrido[4,3-b]carbazole
C16H18N2     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2007          44          539-541
A short synthesis of the hexahydropyrido[4,3-b]carbazole core structure for the synthesis of aspidosperma alkaloids
Yavuz Ergun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

44 .     1-methyl-2-[1-(1,1-dimethylethyl)pentyl]-1H-imidazole
C13H24N2     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2004          41          335-341
Novel nucleophilic CC bond-forming tele-reaction of imidazole ring
Shunsaku Ohta,Kentaro Sato,Ikuo Kawasaki,Yuko Yamaguchi,Satoko Nishio and Masayuki Yamashita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

45 .     compound 9d
C18H21N     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2003          40          113-120
N-phenyl-substituted pyrrolidines,piperidines and azabicyclics by a tandem reduction-double reductive amination reaction
Richard A. Bunce,Derrick M. Herron,Jason R. Lewis and Sharadsrikar V. Kotturi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

46 .     compound 3e
C19H25NO2     ÏàËÆ¶È:50%
Journal of Heterocyclic Chemistry          2001          38          371-377
Inverse electron-demand 1,3-dipolar cycloaddition reactions of cyclooctyne with pyridinium bis(methoxycarbonyl)methylides
Kiyoshi Matsumoto, Naoto Hayashi, Yukio Ikemi, Mitsuo Toda, Takane Uchida, Kinuyo Aoyama and Yoshihiro Miyakoshi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

47 .     methyl 2-[(1R,2R,6R)-6-isopropenyl-2-methoxy-3-methylcyclohex-3-enyl]-2-methyl-propionate
C16H26O3     ÏàËÆ¶È:50%
Indian Journal of Chemistry          2008          47B          1414-1422
Enantiospecific synthesis of (+)-trans-¦Á-himachalene via an intramolecular type II carbonyl ene reaction
Srikrishna,A; Kumar,P Ravi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

48 .     (1R,7R,8R)-8-methoxy-6,6,9-trimethyl-2-methylenebicyclo[5.4.0]undec-9-en-4-ol
C16H26O2     ÏàËÆ¶È:50%
Indian Journal of Chemistry          2008          47B          1414-1422
Enantiospecific synthesis of (+)-trans-¦Á-himachalene via an intramolecular type II carbonyl ene reaction
Srikrishna,A; Kumar,P Ravi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

49 .     3-(9-(Julolidinyl)ethynyl)-6-methylpyridazine
C19H19N3     ÏàËÆ¶È:50%
Heterocycles          2010          81          1445-1457
Rod-Like Conjugated Molecules with Ethynylene Linkage and Pyridazines Moieties: Synthesis and Light Emitting Properties
Caroline Hadad, Catherine Fiol-Petit, Anne-Sophie Cornec, Georges Dupas, Yvan Ramondenc, and Nelly Pl¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

50 .     lyconadin A
    ÏàËÆ¶È:50%
Heterocycles          2009          77          679-729
The Lycopodium Alkaloids
Yusuke Hirasawa, Jun'ichi Kobayashi, and Hiroshi Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

51 .     rac-cis-2-(2-methallyloxy)cyclohexanol
C10H18O2     ÏàËÆ¶È:50%
Heterocycles          2009          77          1123-1146
Synthesis of Annulated 1,4-Dioxanes and Perhydro-1,4-oxazines by Domino-Wacker-Carbonylation and Domino-Wacker-Mizoroki-Heck Reactions
Lutz F. Tietze, Arne Heins, Mohammad Soleiman-Beigi, and Christian Raith
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

52 .     1-(2-methyl-1,2,3,4-tetrahydroisoquinolin-1-yl)cyclohexan-1-ol
C16H23NO     ÏàËÆ¶È:50%
Heterocycles          2004          63          401-409
Alkali Metal-mediated Synthesis of 1- and 4-Substituted N-Alkyl-1,2,3,4-tetrahydroisoquinolines
Ugo Azzena,* Luisa Pisano, and Mario Pittalis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

53 .     Compound 32
C15H20N2O2     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2008          16          1431-1443
Design, synthesis and preliminary pharmacological evaluation of new piperidine and piperazine derivatives as cognition-enhancers
Elisabetta Martini, Carla Ghelardini, Silvia Dei, Luca Guandalini, Dina Manetti, Michele Melchiorre, Monica Norcini, Serena Scapecchi, Elisabetta Teodori, Maria Novella Romanelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

54 .     5-(3-Phenylpropyl)piperidin-2-one
C14H19NO     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2010          93          1180-1186
The Baylis¨CHillman Adducts as Valuable Source for One-Pot Multi-Step Synthesis: A Facile Synthesis of Substituted Piperidin-2-ones
Deevi Basavaiah, Raju Jannapu Reddy and Dandamudi V. Lenin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

55 .     Compound 5 cis
    ÏàËÆ¶È:50%
Magnetic Resonance in Chemistry          2010          48          356-361
Relative acidities and structure analysis of cis and trans isomers of 1, 5-oxazaspiro[5.5] undecane derivatives by multinuclear magnetic resonance (pages 356¨C361)
Jorge Antonio Guerrero-Álvarez, Wendy Paloma Mas-Ku, Cesar Garc¨ªas-Morales and Armando Ariza-Castolo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

56 .     Compound 22
    ÏàËÆ¶È:50%
Magnetic Resonance in Chmesitry          2005          43          1057-1062
Complete 1H and 13C NMR spectral assignment of N-aralkylsulfonamides, N-sulfonyl-1, 2, 3, 4-tetrahydroisoquinolines and N-sulfonyl-2, 3, 4, 5-tetrahydro-1H-2-benzazepines. Conformational analysis of N-[((3', 4'-dichlorophenyl)methyl)sulfonyl]-3-methyl-2,
Jorge L. Jios, Gustavo P. Romanelli, Juan Carlos Autino, H¨¦ctor E. Giaccio, Helmut Duddeck and Michael Wiebcke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

57 .     Compound 2
    ÏàËÆ¶È:50%
Magnetic Resonance in Chmesitry          2002          40          659-665
Phenylselenenylmenthane derivatives and their enantiomeric discrimination by 1H and 13C NMR spectroscopy in the presence of a chiral dirhodium complex
Shahid Malik, Stefan Moeller, Helmut Duddeck and Muhammad Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

58 .     Faurinone
    ÏàËÆ¶È:50%
Phytochemistry          1983          22          1505-1506
A structure of faurinone, a sesquiterpene ketone isolated from valeriana officinalis
R. Bos, H. Hendriks, J. Kloosterman, G. Sipma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

59 .     (R)-1-(1-Hydroxy-3-methylbutan-2-yl)-4-phenyl-1,2,5,6-tetrahydropyridine
    ÏàËÆ¶È:50%
Tetrahedron Letters          2001          42          2063-2068
Solid-phase Zincke route to pyridinium, tetrahydropyridine, and piperidine derivatives: vesamicol analogs
Masahiro Eda, Mark J Kurth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

60 .     (R)-4-(1,1-Dimethylethyl)-1-(1-hydroxy-3-phenylpropan-2-yl)-1,2,5,6-tetrahydropyridine
    ÏàËÆ¶È:50%
Tetrahedron Letters          2001          42          2063-2068
Solid-phase Zincke route to pyridinium, tetrahydropyridine, and piperidine derivatives: vesamicol analogs
Masahiro Eda, Mark J Kurth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

61 .     fragment A
    ÏàËÆ¶È:50%
Tetrahedron Letters          2001          42          6057-6060
Total synthesis of aspirin-triggered 15-epi-lipoxin A4
Ana R Rodrı́guez, Bernd W Spur
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

62 .     compound 6e
    ÏàËÆ¶È:50%
Tetrahedron Letters          2002          43          607-609
Oxazoline azomethine imines preparation and cycloaddition with phenyl isocyanate
Olivier Bedel, Dominique Urban, Yves Langlois
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

63 .     compound 24
    ÏàËÆ¶È:50%
Tetrahedron Letters          2002          43          6975-6978
Towards a total synthesis of guanacastepene A: construction of fully functionalized AB and BC ring segments
Goverdhan Mehta, Jayant D Umarye, Vanessa Gagliardini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

64 .     compound 22
    ÏàËÆ¶È:50%
Tetrahedron Letters          2002          43          8149-8151
Homocoupling of alkyl-, alkenyl-, and arylboronic acids
J.R. Falck, Suchismita Mohapatra, Muralidhar Bondlela, Sylesh K. Venkataraman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

65 .     compound 10b
C16H22S     ÏàËÆ¶È:50%
Tetrahedron Letters          2002          43          9615-9619
Thermal rearrangements of bis-allenyl thiosulfonates. Synthesis of novel thienothiophene and thieno-oxathiine derivatives
Mihail L. Birsa, Marina Cherkinsky, Samuel Braverman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

66 .     compound cis-3a
    ÏàËÆ¶È:50%
Tetrahedron Letters          2003          44          6809-6812
Clean and atom-economic synthesis of octahydroacridines: application to essential oil of citronella
Raquel G Jacob, Gelson Perin, Giancarlo V Botteselle, Eder J Lenardão
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

67 .     compound 2e
    ÏàËÆ¶È:50%
Tetrahedron Letters          2003          44          9169-9171
A simple and fast procedure for efficient synthesis of ¦Â- and ¦Ã-azidoarylketones
Pradeep N.D. Singh, Sivaramakrishnan Muthukrishnan, Rajesh S. Murthy, Rodney F. Klima, Sarah M. Mandel, Michael Hawk, Nina Yarbrough, Anna D. Gudmundsd¨®ttir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

68 .     compound 7
C16H25N     ÏàËÆ¶È:50%
Tetrahedron Letters          2004          45          3565-3568
Stereoselective synthesis of activated cyclopropanes with an ¦Á-pyridinium acetamide bearing an 8-phenylmenthyl group as the chiral auxiliary
Satoshi Kojima, Kyoko Hiroike, Katsuo Ohkata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

69 .     compound 19
C16H26O3     ÏàËÆ¶È:50%
Tetrahedron Letters          2004          45          6867-6870
Enantiospecific first total synthesis of (+)-trans-¦Á-himachalene
A. Srikrishna, P. Ravi Kumar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

70 .     compound 24
C16H26O2     ÏàËÆ¶È:50%
Tetrahedron Letters          2004          45          6867-6870
Enantiospecific first total synthesis of (+)-trans-¦Á-himachalene
A. Srikrishna, P. Ravi Kumar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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71 .     compound 2b
    ÏàËÆ¶È:50%
Tetrahedron Letters          2004          45          6733-6736
Access to novel substituted diazaadamantanes via semi-natural tetrahydrocytisine
Alexandre V. Ivachtchenko, Alexandre Khvat, Sergey E. Tkachenko, Yuri B. Sandulenko, Vladimir Y. Vvedensky
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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72 .     5-Fluoro-1,2,3,4-tetrahydroacridine
C13H12FN     ÏàËÆ¶È:50%
Tetrahedron Letters          2005          46          767-770
Synthesis of regiospecifically substituted quinolines from anilines
Giorgio Chelucci, Ilaria Manca, Gerard A. Pinna
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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73 .     compound 3a
    ÏàËÆ¶È:50%
Tetrahedron Letters          2005          46          1039-1044
Ionic liquid accelerated intramolecular hetero-Diels-Alder reactions: a protocol for the synthesis of octahydroacridines
J.S. Yadav, B.V.S. Reddy, Lakshindra Chetia, G. Srinivasulu, A.C. Kunwar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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74 .     ÃÀà­Ëûàº
    ÏàËÆ¶È:50%
Chinese Journal of Medicinal Chemistry          2007          17          314-315
Liposoluble constituents of Dracocephalum tanguticum Maxim. (I)
ZHENG Hong-ting, ZHANG Guo-gang, ZHENG Ya-fu, JIN Yin-ping, DU Shu-shan, DENG Zhi-wei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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75 .     compound 13
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          1994          2          1423-1434
Structure¡ªactivity studies leading to potent chloride channel blockers: 5e-tert-butyl-2-[4-(substituted-ethynyl)phenyl]-1,3-dithianes
Qing X. Li, John E. Casida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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76 .     1-Phthalimido-7-[[N-ethyl-N-[(2-mesitylene) sulfonyl]-amino]-4-azaheptane
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          1996          4          825-836
Synthesis and evaluation of a polyamine phosphinate and phosphonamidate as transition-state analogue inhibitors of spermidine/spermine-N1-acetyltransferase
Ronghui Wu, Nada H. Saab, Huatao Huang, Laurie Wiest, Anthony E. Pegg, Robert A. Casero Jr, Patrick M. Woster
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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77 .     9-Methoxycarbonylnonyltriphenylphosphonium bromide
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          1997          5          1267-1274
Identification and biosynthesis of (E,E)-10,12-tetradecadienyl acetate in Spodoptera littoralis female sex pheromone gland
Isabel Navarro, Esther Mas, Gemma Fabri¨¤s, Francisco Camps
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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78 .     7-[4-Hydroxybutyl]-1,2,3,4-tetrahydronaphthalene-1-one
C14H18O2     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          1998          6          2421-2439
The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewisx
Paul V. Murphy, Rod E. Hubbard, David T. Manallack, Ruth E. Wills, John G. Montana, Richard J.K. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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79 .     7-Carboxypropyl-1,2,3,4-tetrahydronaphthalene-1-one
C14H16O3     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          1998          6          2421-2439
The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewisx
Paul V. Murphy, Rod E. Hubbard, David T. Manallack, Ruth E. Wills, John G. Montana, Richard J.K. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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80 .     6-Carboxypropyl-1,2,3,4-tetrahydronaphthalene
C14H18O2     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          1998          6          2421-2439
The design, synthesis, and evaluation of novel conformationally rigid analogues of sialyl Lewisx
Paul V. Murphy, Rod E. Hubbard, David T. Manallack, Ruth E. Wills, John G. Montana, Richard J.K. Taylor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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81 .     (2S,2aR,6S,7aS,7bS,8R,9S)-7b-(1-Butenyl)hexahydro-9-methyl-4H-2,2,6-(epoxy[1]propanyl[3]ylidene)furo[2,3,4-gh]pyrrolizin-10-one
C16H21NO3     ÏàËÆ¶È:50%
Tetrahedron          2012          68          598-602
Oxidation of acyclic alkenes and allyl and benzyl ethers with DIB/t-BuOOH/Mg(OAc)2
Thanapat Sastraruji, Stephen G. Pyne, Alison T. Ung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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82 .     1-Nitro-N-tosylnonan-2-amine
C16H26N2O4S     ÏàËÆ¶È:50%
Tetrahedron          2012          68          1736-1744
The use of samarium or sodium iodide salts as an alternative for the aza-Henry reaction
Humberto Rodr¨ªguez-Solla, Carmen Concell¨®n, Noem¨ª Alvaredo, Raquel G. Soengas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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83 .     (20R)-24-Methylenecholestane-3¦Â,21-diol
    ÏàËÆ¶È:50%
Journal of the Chemical Society, Perkin Transactions 1          1984                   2277-2282
Steroids from the starfish Euretaster insignis: a novel group of sulphated 3¦Â,21-dihydroxysteroids
Maria V. D'Auria, Ester Finamore, Luigi Minale, Cosimo Pizza, Raffaele Riccio, Franco Zollo, Michelle Pusset and Philippe Tirard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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84 .     compound 1bc
C21H30N4O4F6     ÏàËÆ¶È:50%
Heterocycles          2000          53          1317-1328
Solution Parallel Synthesis of Cyclic Guanidines
Christelle Marmillon, Jacques Bompart, Mich¨¨le Calas, Roger Escale,* and Pierre-Antoine Bonnet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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85 .     (1S,5R)-6-isopropylidine-1,5-dimethylbicyclo-[3.3.0]octan-3-one
C13H20O     ÏàËÆ¶È:50%
Indian Journal of Chemistry          2011          50B          1092-1106
Enantiospecific first total synthesis of cucumin-H
Srikrishna, A; Dethe, Dattatraya H
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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86 .     methyl 2,6-dimethyl-10-oxoundeca-(2E,6Z)-dienoate
    ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2005          41          1228-1229
ChemicallyRationalApproachtotheSynthesisofPrecursorsofthe¡°Prenyl¡±FragmentinEpothilones
F.A. Gimalova, Z.A. Yusupov, T.A. Maslova and M.S. Miftakhov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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87 .     5-exo-acetoxy-2,2,3-exotrimethylbicyclo[2.2.1]-heptane
C12H20O2     ÏàËÆ¶È:50%
Russian Journal of Organic Chemistry          2001          37          1418-1429
Reactions of Some Terpenes and Their Derivatives with Acylating Agents in the Presence of Aluminosilicate Catalysts
K. P. Volcho, L. E. Tatarova, E. V. Suslov, D. V. Korchagina and N. F. Salakhutdinov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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88 .     compound 2
    ÏàËÆ¶È:50%
Organic Magnetic Resonance          1983          21          122-124
Differentiation of diastereomeric bornane derivatives by 13C NMR spectroscopy
Helmut Duddeck, Blagoy Blagoev, Nikolina D. Berova and Vassil Vassilev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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89 .     compound 1
    ÏàËÆ¶È:50%
Organic Magnetic Resonance          1982          19          95-97
The assignment of 13C NMR shift data in clerodanes and related structures
J. M. Luteijn, A. Van Veldhuizen and A. De Groot
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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90 .     N-tert-Butoxycarbonyl-5-(hexylthiomethyl)pyrrolidin-2-one
C16H29NO3S     ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2011          19          5500-5506
Substituted lactam and cyclic azahemiacetals modulate Pseudomonas aeruginosa quorum sensing
Venkata L.A. Malladi, Adam J. Sobczak, Natalie Maricic, Senthil Kumar Murugapiran, Lisa Schneper, John Makemson, Kalai Mathee, Stanislaw F. Wnuk
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2012-05-10 19:26:16
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kaola0916

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4Â¥: Originally posted by chzhbin at 2012-06-06 23:58:39
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5Â¥2012-06-07 09:18:38
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