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20.98, 22.82, 24.07, 24.56, 27.44, 29.49, 30.73, 35.79, 37.79, 46.83, 49.92, 51.85, 72.04, 72.24, 73.28, 82.41, 170.24
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1 .     orientalol E 6-acetate
C17H28O4     ÏàËÆ¶È:64.7%
Phytochemistry          2003          63          877-881
Guaiane-type sesquiterpenoids from Alisma orientalis
Guo-Ping Peng, Gang Tian, Xian-Feng Huang, Feng-Chang Lou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     cyclokessyl acetate
    ÏàËÆ¶È:64.7%
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
3 .     compound 7b
    ÏàËÆ¶È:64.7%
Tetrahedron Letters          2003          44          579-582
A new diorganozinc-based enantioselective access to truncated d-ribo-phytosphingosine
Tahar Ayad, Yves G¨¦nisson, Alexandre Verdu, Michel Baltas, Liliane Gorrichon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3-Acetylamino-4-hydroxy-1,1-dioxo-tetrahydro-1¦Ë6-thiophene-3-carboxylic acid
C17H29NO6S     ÏàËÆ¶È:64.7%
Tetrahedron          2012          68          208-213
1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes
Nikla Baricordi, Simonetta Benetti, Valerio Bertolasi, Carmela De Risi, Gian P. Pollini, Francesco Zamberlan, Vinicio Zanirato
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     orientalol E 6-acetate
    ÏàËÆ¶È:64.7%
Natural Product Research and Development          2001          13(3)          1-3
CHEMICAL STUDIES ON ALISMA ORIENTALIS JUZEP.
PENG Guo ping; LOU Feng chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     5(11)-epoxycadinane-4¦Â,5¦Â,10¦Â,11-tetraol
C15H26O3     ÏàËÆ¶È:64.7%
Planta Medica          2012          78          1010-1014
Sesquiterpenoids from the Rhizomes of Homalomena occulta
Xie, Xiao-Yu; Wang, Rui; Shi, Yan-Ping:
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1-[N-[[(3R)-3-[[(2-Methylpropyl)amino]carbonyl]-(2R)-2-aziridinyl]carbonyl]-L-leucyl]-L-proline
C19H32N4O5     ÏàËÆ¶È:64.7%
Journal of Medicinal Chemistry          1995          38          3078-3085
Aziridine Analogs of [[trans-(Epoxysuccinyl)-L-leucyl]amino]-4-guanidinobutane (E-64) as Inhibitors of Cysteine Proteases
Valeri Martichonok, Celine Plouffe, Andrew C. Storer, Robert Menard, J. Bryan Jones
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 5a
    ÏàËÆ¶È:64.7%
Indian Journal of Chemistry          1995          34B          992-993
13C NMR assignments of ¦Á- and ¦Â-dihydroartemisinin
Ashish Kumar Pathak, Dharam C Jain & Ram P Sharma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     rumphellclovane E
C15H24O3     ÏàËÆ¶È:64.7%
Tetrahedron          2013          69          2740-2744
Rumphellclovanes C¨CE, new clovane-type sesquiterpenoids from the gorgonian coral Rumphella antipathies
Hsu-Ming Chung, Jui-Hsin Su, Tsong-Long Hwang, Jan-Jung Li, Jih-Jung Chen, Yung-Husan Chen, Yu-Chia Chang, Yin-Di Su, Yu-Hsin Chen, Lee-Shing Fang, Jyh-Horng Sheu, Wei-Hsien Wang, Ping-Jyun Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     8¦Â-acetoxy-10¦Á-oxyethyl-guaia-4¦Á,11diol
C19H34O5     ÏàËÆ¶È:63.1%
Chinese Chemical Letters          2004          15          791-793
A New Sesquiterpenoid from Magnolia delavayi
Jian Xin CAO, Guo Fang LAI, Yi Feng WANG, Yuan Feng HUANG, Shi De LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     17-epioxandrolone
C19H32O3     ÏàËÆ¶È:63.1%
Steroids          1992          57          306-312
Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17¦Á-methyl steroids: synthesis and rearrangement
Honggang Bi, Robert Mass¨¦, George Just
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     17-Epioxandrolone
    ÏàËÆ¶È:63.1%
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
13 .     (1S)-1-C-[4-(adamant-1-ylmethoxy)butyl]-N-butyl-1-deoxynojirimycin
C25H45NO5     ÏàËÆ¶È:63.1%
European Journal of Organic Chemistry          2010                   1258-1283
Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism
Tom Wennekes, Richard J. B. H. N. van den Berg, Thomas J. Boltje, Wilma E. Donker-Koopman, Bastiaan Kuijper, Gijsbert A. van der Marel, Anneke Strijland, Carlo P. Verhagen, Johannes M. F. G. Aerts and Herman S. Overkleeft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     4-acetoxy-3-acetylamino-1,1-dioxo-tetrahydro-1¦Ë6-thiophene-3-carboxylic acid
C19H31NO7S     ÏàËÆ¶È:61.1%
Tetrahedron          2012          68          208-213
1,4-Dithiane-2,5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes
Nikla Baricordi, Simonetta Benetti, Valerio Bertolasi, Carmela De Risi, Gian P. Pollini, Francesco Zamberlan, Vinicio Zanirato
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (2S,3S,4R)-2-Acetamido-1,3,4-triacetoxyhexadecane
C24H43NO7     ÏàËÆ¶È:61.1%
European Journal of Organic Chemistry          1988          1988          619-625
Biologically active glycosides from asteroidea, XV. Asymmetric synthesis of phytosphingosine and phytosphingosine anhydro base: Assignment of the absolute stereochemistry
Shigeo Sugiyama, Masanori Honda and Tetsuya Komori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     13,18-dihydroxystemodan-2-one
    ÏàËÆ¶È:60%
Phytochemistry          2002          59          57-62
Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
Avril R.M. Chen, Paul B. Reese
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3-oxo-4¦Â-hydroxy-5¦Â,10¦Â-cis-17¦Á,20¦Á-cleroda-13(14)-en-15,16-olide
C20H30O4     ÏàËÆ¶È:60%
Phytochemistry          1988          27          3187-3196
Terpenoids from Ageratina saltillensis
Nianbai Fang,Sanggong Yu,Tom J. Mabry,Khalil A. Abboud,Stanley H. Simonsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (1S)-N-[5-(adamant-1-ylmethoxy)pentyl]-1-C-butyl-1-deoxynojirimycin
C26H48NO5     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          2010                   1258-1283
Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism
Tom Wennekes, Richard J. B. H. N. van den Berg, Thomas J. Boltje, Wilma E. Donker-Koopman, Bastiaan Kuijper, Gijsbert A. van der Marel, Anneke Strijland, Carlo P. Verhagen, Johannes M. F. G. Aerts and Herman S. Overkleeft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     (1S)-1-C-[5-(adamant-1-ylmethoxy)pentyl]-1-deoxy-N-hexylnojirimycin
C28H51NO5     ÏàËÆ¶È:59.0%
European Journal of Organic Chemistry          2010                   1258-1283
Synthesis and Evaluation of Lipophilic Aza-C-glycosides as Inhibitors of Glucosylceramide Metabolism
Tom Wennekes, Richard J. B. H. N. van den Berg, Thomas J. Boltje, Wilma E. Donker-Koopman, Bastiaan Kuijper, Gijsbert A. van der Marel, Anneke Strijland, Carlo P. Verhagen, Johannes M. F. G. Aerts and Herman S. Overkleeft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     3¦Â,20R-bis(acetoxy)-5¦Â-12¦Á-hydroxy-pregn-14-ene
C25H38O5     ÏàËÆ¶È:59.0%
Steroids          2011          76          1166-1175
Norrish¨CPrins reaction as a key step in the synthesis of 14¦Â-hydroxy-5¦Á (or 5¦Â or ¦¤5,6)-pregnane derivatives
Philippe Geoffroy, Blandine Ressault, Eric Marchioni, Michel Miesch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (-)-Cumacrene, (4S)-4-[(1R,2S)-2-isopropenyl-1-methylcyclobutyl]-1-methylcyclohexene
C15H24     ÏàËÆ¶È:58.8%
Phytochemistry          2005          66          249-260
Sesquiterpenes from Cupressus macrocarpa foliage
Laurence G. Cool
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (1R,4S,5R,7R,10S)-1,11-dihydroxyeudesman-14,4-olide
C15H24O4     ÏàËÆ¶È:58.8%
Phytochemistry          2003                   1003-1011
Polar constituents of celery seed
Junichi Kitajima, Toru Ishikawa, Mitsuru Satoh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     5(9),6-tricyclohumulane-4¦Á,8¦Á,10¦Á-triol
    ÏàËÆ¶È:58.8%
Phytochemistry          2002          59          39-44
Microbial metabolism of partheniol by Mucor circinelloides
Galal T. Maatooq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     10-bromo-9-hydroxy-chamigra-2,7(14)-diene
C15H23BrO     ÏàËÆ¶È:58.8%
Phytochemistry          2001          58          517-523
Halogenated metabolites with antibacterial activity from the Okinawan Laurencia species
Charles Santhanaraju Vairappan, Minoru Suzuki, Tsuyoshi Abe, Michio Masuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     (1S,4S,5S,6R,7S,8S,9R,10S)-1-acetoxy-9-benzoyloxy-8-cinnamoyloxy-4,6-dihydroxydihydro-¦Â-agarofuran
C33H38O9     ÏàËÆ¶È:58.8%
Journal of Natural Products          2008          71(8)          1331-1335
Sesquiterpenes from Celastrus vulcanicola as Photosynthetic Inhibitors
David Torres-Romero, Beatriz King-D¨ªaz, Ignacio A.Jim¨¦nez, Blas Lotina-Hennsen, and Isabel L. Bazzocchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     lepadiformine C
C16H29N     ÏàËÆ¶È:58.8%
Journal of Natural Products          2006          69(4)          558-562
Sensitivity of Cardiac Background Inward Rectifying K Outward Current (IK1) to the Alkaloids Lepadiformines A, B, and C
Martin-Pierre Sauviat, Joseph Vercauteren, Nicole Grimaud, Marcel Jug, Mohamed Nabil, Jean-Yves Petit, and Jean-Franois Biard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     1¦Á,6¦Â-dihydroxyambrox
C16H28O3     ÏàËÆ¶È:58.8%
Journal of Natural Products          2006          69(6)          957-959
Biotransformation of (−-Ambrox by Cell Suspension Cultures of Actinidia deliciosa
Asma Nasib, Syed Ghulam Musharraf, Sajjad Hussain, Saifullah Khan,Shazia Anjum, Shamsher Ali, Atta-ur-Rahman, and M. Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     dihydrobotrydialone
    ÏàËÆ¶È:58.8%
Journal of Natural Products          2000          63          182-184
Secobotrytriendiol and Related Sesquiterpenoids: New Phytotoxic Metabolites from Botrytis cinerea
Rosa Dur¨¢n-Patr¨®n, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     arnimollin acetate
    ÏàËÆ¶È:58.8%
Planta Medica          1990          56          104-110
Germacranolides, Guaianolides, and Xanthanolides from the Flowers of Arnica moths and an X-Ray Structure Analysis of Baileyin Acetate
Christoph Marcinek-Hupen-Bestendonk,G¨¹nter Willuhn,Alots Steigel,Detlef Wendisch,BirgitMiddelhauve, Michael Wiebcke and Dietrich Mootz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     1(S*)-hydroxy-¦Á-bisabolo1oxide A acetate
C17H28O4     ÏàËÆ¶È:58.8%
Planta Medica          1988          54          463-464
¦Á-Bisabololoxide Derivatives from Artemisia abrotanum
A. H. Mericli, B. cubukcu, J. Jakupovict , and N. Ozhatay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     ananosmin acetate
    ÏàËÆ¶È:58.8%
Acta Botanica Yunnanica          1993          15(2)          196-200
SESQUITERPENOIDS FROM KADSURA ANANOSMA
ZOU Cheng,PU Xiang-Yu,ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     compound 1
C15H26O2     ÏàËÆ¶È:58.8%
Chemical & Pharmaceutical Bulletin          1990          38          1405-1407
Studies on the Sesquiterpenoids of Panax ginseng C. A. MEYER. IV
Hisakatsu IWABUCHI,Nobuo KATO and Masahiro YOSHIKURA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     panasinsanol A
C15H26O     ÏàËÆ¶È:58.8%
Chemical & Pharmaceutical Bulletin          1987          35          1975-1981
Studies on the Sesquiterpenoids of Panax ginseng C. A. MEYER. Isolation and Structure Determination of Sesquiterpene Alcohols, Panasinsanols A and B
HISAKATSU IWABUCHI,MASAHIRO YOSHIKURA,YOSHITOMI IKAWA and WASUKE KAMISAKO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     panasinsanol B
C15H26O     ÏàËÆ¶È:58.8%
Chemical & Pharmaceutical Bulletin          1987          35          1975-1981
Studies on the Sesquiterpenoids of Panax ginseng C. A. MEYER. Isolation and Structure Determination of Sesquiterpene Alcohols, Panasinsanols A and B
HISAKATSU IWABUCHI,MASAHIRO YOSHIKURA,YOSHITOMI IKAWA and WASUKE KAMISAKO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     4¦Á,10¦Á-dihydroxy-5¦Â-H-guaj-6-en
    ÏàËÆ¶È:58.8%
China Journal of Chinese Materia Medica          2009          34          994-998
Chemical constituents of A lisma orientalis and their immunosuppressive function
ZHANG Chaofeng, ZHOU Aichun, ZHANG mian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     (5S)-5-hydroxyacetylcaespitol
C17H27Br2ClO4     ÏàËÆ¶È:58.8%
Journal of Natural Products          2010          73          27-32
Cytotoxic Halogenated Metabolites from the Brazilian Red Alga Laurencia catarinensis
Cintia Lhullier, Miriam Falkenberg, Efstathia Ioannou, Antonio Quesada, Panagiota Papazafiri, Paulo Antunes Horta, Eloir Paulo Schenkel, Constantinos Vagias and Vassilios Roussis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     3¦Â-acetoxyoplopanone
C17H28O4     ÏàËÆ¶È:58.8%
Phytochemistry          1997          46          1039-1043
Sesquiterpenoids from Pallenis spinosa
Giovanni Appendino, Jasmin Jakupovic, Sven Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     1¦Â,15-diacetoxy-4¦Á,6¦Â-dihydroxyeudesmane
    ÏàËÆ¶È:58.8%
Journal of Natural Products          1988          Vol 51          475
Epoxidation Reaction of 6¦Â-Acetoxyeudesmenes and Acid-catalyzed Transformations of the Epoxy Compounds
E. Cabrera, A. Garcia-Granados, M. A. Quecuty
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     pyrazoline
C17H26O2N2     ÏàËÆ¶È:58.8%
Journal of Natural Products          1993          Vol 56          857
Preparation of a Cyclopropane-Containing Analogue of Artemisinin
Soo-Un Kim, Jin-Hyuk Choi, Sang Soo Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     10-epi-Dihydrobotrydial
C17H28O5     ÏàËÆ¶È:58.8%
Phytochemistry          1996          41          513-517
Biologically active sesquiterpenoid metabolites from the fungus Botrytis cinerea
Isidro G. Collado, Rosario Hern¨¢ndez-Gal¨¢n, Victoria Prieto, James R. Hanson, Laureana G. Rebordinos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     1¦Â-Acetoxy-3-eudesmen-11-ol
C17H28O3     ÏàËÆ¶È:58.8%
Phytochemistry          1995          39          603-607
Sesquiterpenes from leaves of Cryptomeria japonica
Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     compound(ref 2)
    ÏàËÆ¶È:58.8%
Phytochemistry          1994          37          597-623(604)
The daucane (carotane) class of sesquiterpenes
Emilio L. Ghisalberti
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     9-O-Acetylseiricardine B
C17H28O3     ÏàËÆ¶È:58.8%
Phytochemistry          1993          33          69-78
Seiricardines B and C, phytotoxic sesquiterpenes from three species of Seiridium pathogenic for cypress
Antonio Evidente, Andrea Motta, Lorenzo Sparapano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     intrlcatetraol diacetate
C34H58Br2Cl2O8     ÏàËÆ¶È:58.8%
Phytochemistry          1993          33          651-656
Intricatetraol, a halogenated triterpene alcohol from the red alga Laurencia intricata
Minoru Suzuki, Yoshihide Matsuo, Satoshi Takeda, Teruaki Suzuki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     isotrichodiol
    ÏàËÆ¶È:58.8%
Phytochemistry          1991          30          2237-2243
Biosynthesis of trichothecene mycotoxins: Identification of isotrichodiol as a post-trichodiene intermediate
Andrew R. Hesketh, Linden Gledhill, David C. Marsh, Barrie W. Bycroft, Paul M. Dewick, John Gilbert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     9-Epi-myrionine
C15H26N2O     ÏàËÆ¶È:58.8%
Organic Letters          2007          Vol. 9, No. 18          3531-3534
Solution and Crystal Conformations of Myrionine, a New 8¦Â-Alkyl-cis-decahydroquinoline of Myrioneuron nutans
Van Cuong Pham, Akino Jossang, Ang¨¨le Chiaroni, Thierry S¨¦venet,Van Hung Nguyen, and Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     (3S,5aR,6aS,7aS)-5,5a,6,6a,7,7a-Hexahydro-3-isobutyl-3,6,6,7a-tetramethylbicyclo[4.1.0]hept-1(6)-eno[3,4-b][1,4]oxazin-2(3H)-one
C17H27NO2     ÏàËÆ¶È:58.8%
The Journal of Organic Chemistry          2011          76          1621-1633
Asymmetric Synthesis of r-Methyl-r-Amino Acids via Diastereoselective Alkylation of (1S)-(+)-3-Carene Derived Tricyclic Iminolactone
Ta-Jung Lu and Cheng-Kun Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     compound 3
C16H25NO5S     ÏàËÆ¶È:58.8%
Tetrahedron Letters          2000          41          7289-7292
Synthesis of the first enantiomerically pure 3-thiazolines via Asinger reaction
Imre Schlemminger, Hans-Hermann Janknecht, Wolfgang Maison, Wolfgang Saak, J¨¹rgen Martens
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     7,15-dihydroxybisabol-10-ene acetate
C17H28O2     ÏàËÆ¶È:58.8%
Phytochemistry          1989          28          531-542
ent-clerodanes and other constituents from bolivian Baccharis species
C. Zdero,F. Bohlmann,J.C. Solomon,R.M. King,H. Robinson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     1-hydroxy-¦Á-bisabololoxide A acetaee
    ÏàËÆ¶È:58.8%
Phytochemistry          1989          28          2163-2167
Sesquiterpene lactones from Artemisia hispanica
Juan F. Sanz,Oscar Barbera,J.Alberto Marco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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