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qqzhao: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2014-04-15 16:38:32
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1 .     1(10)-en-2-oxo-7¦Á-isopropanoleremophilane
C15H24O2     ÏàËÆ¶È:93.3%
Chemical Research in Chinese Universities          2009          25          480-482
Two Eremophilane-type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana(Hemsl.) Greenm
WANG Cai-fang, ZHAO Yu, LIU Yan-ze and ZHANG Zhen-zhong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     (rel)-4¦Â,5¦Â,7¦Â-eremophil-1(10)-en-2-oxo-12-oic acid
    ÏàËÆ¶È:80%
Qu¨ªmica Nova          2013          36          1008-1013
SESQUITERPENOS DE Ocotea lancifolia (Lauraceae)
Maria Jos¨¦ de Camargo, Mayker Lazaro Dantas Miranda, Camila Miyuki Kagamida, Edilene Delphino Rodrigues,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     viridiflorol
C15H26O     ÏàËÆ¶È:66.6%
Acta Botanica Boreali-Occidentalia Sinica          2006          26          2146-2149
Liposoluble Constituents in Eucalyptus globulus Labill. Fruits
TAN MAN-Liang, WANG Ye, ZHOU Li-gang, JIANG Wei-bo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     5¦Á-hydroxyisopterocarpolone
C15H24O3     ÏàËÆ¶È:66.6%
Phytochemistry          1996          43          815-817
Eudesmane sesquiterpenes from Artemisia eriopoda
Jin-Feng Hu, Su-Ping Bai, Zhong-Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     7-epiglobulol
C15H26O2     ÏàËÆ¶È:66.6%
Phytochemistry          1994          37          1023-1025
The hydroxylation of globulol and 7-epiglobulol by Cephalosporium aphidicola
James R. Hanson, Peter B. Hitchcock, Revathy Manickavasagar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (+)-5¦Á-Hydroxy-isop terocarpo lone
    ÏàËÆ¶È:66.6%
Chemical Journal of Chinese Universities          2005          26          1281-1283
Total Syn thes is of 5¦Á-Hydroxy-isopterocarpolone
GUAN Yu-Kun,LI Ping,ZHOU Gang,GAO Xiao-Lei,LI Yu-Lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     4-epi-globulol
C15H26O     ÏàËÆ¶È:66.6%
Journal of the Brazilian Chemical Society          1990          1          105-109
Composition of the Essential Oil of Vassoura.
Carmen Lucia Queiroga, Alberto Fukai and Anita J. Marsaioli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (-)-10-epi-Globulol
    ÏàËÆ¶È:66.6%
European Journal of Organic Chemistry          1995          1995          1039-1043
New sesquiterpene ethers and other constituents isolated from Brazilian vassoura oil
Peter Weyerstahl, Christian Christiansen and Helga Marschall
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     norlongilactone
    ÏàËÆ¶È:66.6%
China Journal of Chinese Materia Medica          2012          37          1973-1976
Sesquiterpenes and monoterpene from Aquilaria sinensis
YANG Lin; QIAO Lirui; XIE Dan; DAI Jungui; GUO Shunxing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     methyl 3-oxoartemisinate structure
C16H22O3     ÏàËÆ¶È:62.5%
Planta Medica          1996          62          359-360
Production of Methyl 3-Oxoartemisinate from Methyl Artemisinate by Suspension Cell Culture of Mentha piperita
Soo-Un Kim and Hyung-Jin Kwon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (7¦Á,9¦Á,10¦Á)-9,10-epoxy-eremophilan-11-ol
C15H26O2     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2008          Vol. 91          1712
Two New Eremophilane-Type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana (Hemsl.) Greenm
Cai-FangWang, Yu Zhao, Yan-Ze Liu, and Zhen-Zhong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     rhombidiol
C15H26O2     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2005          53(2)          238-240
Eudesmane Sesquiterpenes from the Aquatic Fungus Beltrania rhombica
Vatcharin RUKACHAISIRIKUL, Chutanat KAEWBUMRUNG,Souwalak PHONGPAICHIT,and Zubaidah HAJIWANGOH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     cadinane-4¦Â,5¦Á,10¦Â-triol
C15H28O3     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2003          51(8)          986-989
Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA
Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     muurolane-4¦Â,5¦Â,10¦Â-triol
C15H28O3     ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          2003          51(8)          986-989
Cadinane-Type Sesquiterpenes from the Roots of Taiwania cryptomerioides HAYATA
Yueh-Hsiung KUO, Chiou-Fung CHYU, and Hsiu-Chuan LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (-)1¦Â,4¦Â,6¦Átrihydroxy-eudesmane
C15H28O3     ÏàËÆ¶È:60%
Phytochemistry          2008          69          2367-2373
Sesquiterpenoids from Homalomena occulta affect osteoblast proliferation,differentiation and mineralization in vitro
Yong-Mei Hu, Chuan Liu, Ka-Wing Cheng, Herman H.-Y. Sung, Lan D. Williams,Zhong-Lin Yang Wen-Cai Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (()-3,7,11-trimethyl-10-dodecen-1,7-diol
    ÏàËÆ¶È:60%
Journal of Natural Products          2002          65          1319-1322
African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol
Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (4Z,8¦Á,11S)-caryophyll-4(5)-ene-8,14-diol
C15H26O2     ÏàËÆ¶È:60%
Journal of Natural Products          2000          63          44-47
Biotransformation of (4E,8R)-Caryophyll-4(5)-en-8-ol by Botrytis cinerea
Rosa Dur¨¢n-Patr¨®n, Josefina Aleu, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     10¦Á-hydroxyamorphan-4-en-3-one
C15H24O2     ÏàËÆ¶È:60%
Journal of Natural Products          1997          60          38-40
Bioactive Compounds from Taiwania cryptomerioides
Kan He, Lu Zeng, Guoen Shi, Geng-Xian Zhao, John F. Kozlowski, and Jerry L. McLaughlin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     zingiberene-3,6-¦Á-endoperoxide
C15H24O2     ÏàËÆ¶È:60%
Planta Medica          1996          62          565-566
Sesquiterpene Peroxides from Senecio selloi and Eupatorium rufescens
G. R¨¹cker, E. P. Scherikel, D. Manns, R. Mayer,K. Heiden, and B. M. Heinzmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     4¦Â,5¦Á, 10¦Â-trihydroxycadinane
C15H26O2     ÏàËÆ¶È:60%
Planta Medica          1997          63          250-254
Minor Components with Smooth Muscle Relaxing Properties from Scented Myrrh (Commiphora guidotti)
Maria Andersson, Ola Bergendorff, Rudong Shan, Peter Zygmunt, and OIov Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     Pterodontic acid
C15H22O2     ÏàËÆ¶È:60%
Acta Botanica Yunnanica          1996          18£¨3£©          349-352
FOUR NEW SESQUITERPENOIDS FROM LAGGERA PTERODONTA
LI Shun-Lin, DING Jing-Kai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (2RS,4RS,6SR)-2-Cyclohexyltetrahydro-6-(2-methylprop-1-en-1-yl)-2H-pyran-4-ol
C15H26O2     ÏàËÆ¶È:60%
Helvetica Chimica Acta          2009          92          1333-1340
Alkyl-Group Selection in an Acidic-Surfactant-Promoted Reaction of Homoallyl Alcohols and Aldehydes in Water
Takanori Hatakeyama, Yuki Chisaka, Chiaki Kuroda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     laggerone B
    ÏàËÆ¶È:60%
Chinese Chemical Letters          1996          7          1093-1094
EUDESMANES AND EUDESMANOIC GLUCOSIDES FROM LAGGERA PETERODONTA
YU ZHAO,JIAN MIN YUE,JING KAI DING,ZHONG WEN LIN AND HAN DONG SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (-)-10¦Â-hydroxy-4-muurolen-3-one C
C15H24O2     ÏàËÆ¶È:60%
Chinese Chemical Letters          2008          19          1265-1267
First total synthesis of 10¦Á-hydroxy-4-muurolen-3-one and its C10-isomer
Fu Qiang Bi, Li Jing Fang, Chen Xi Zhang, Yu Lin Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     valerianol
    ÏàËÆ¶È:60%
Phytochemistry          1999          52          1063-1067
The hydroxylation of the sesquiterpenoid valerianol by Mucor plumbeus
Simone Fontes Arantes, James R. Hanson, Peter B. Hitchcock
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     1,4-epidioxy-bisabola-2,10-diene(1S,4R,6R)
C15H24O     ÏàËÆ¶È:60%
Phytochemistry          1997          45          537-544
Oxygenated bisabolanes from Alpinia densibracteata
Lai-King Sy, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     5¦Á,11-dihydroxy-3-ene-dudesman-2-one
C15H24O3     ÏàËÆ¶È:60%
Phytochemistry          1997          44          459-464
Eudesmane sesquiterpenes from Laggera pterodonta
Yu Zhao, Jianmin Yue, Zhongwen Lin, Jingkai Ding, Handong Sun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     (¡À)-[1S-(1¦Â,4¦Â,4a¦Â,6¦Â,8a¦Á]-7-Chloro-1,6-di-methyl-4-(1-methylethyl)-1,2,3,4,4a,5,6,7,8,8a-decahydro-l,6-naphthalenediol
    ÏàËÆ¶È:60%
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
29 .     6-isocedrol
    ÏàËÆ¶È:60%
Journal of Natural Products          1984          Vol 47          924-933
13C-nmr Study of Cedrol, 6-Isocedrol, and ¦Á-Cedrene
P. Joseph-Nathan, R. L. Santillan, A. Guti¨¦rrez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     6-isocedrol
    ÏàËÆ¶È:60%
Journal of Natural Products          1986          Vol 49          79
13C-nmr Studies of Cedranolides
P. Joseph-Nathan, A. Guti¨¦rrez, J. D. Hern¨¢ndez, L. U. Rom¨¢n, R. L. Santillan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     8-Epicedrol
    ÏàËÆ¶È:60%
Phytochemistry          1995          39          1081-1084
The biotransformation of 8-epicedrol and some relatives by Cephalosporium aphidicola
Estelle Gand, James R. Hanson, Habib Nasir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     ent-halima-5(10),13-dien-16,15-olide
C20H30O2     ÏàËÆ¶È:60%
Phytochemistry          1995          38          189-194
Clerodane and ent-halimane diterpenes from polyalthia longifolia
Noriyuki Hara, Hitomi Asaki, Yoshinori Fujimoto, Yogesh Kumar Gupta, Ashish Kumar Singh, Mahendra Sahai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     3-oxofabiaimbricatan
C15H24O2     ÏàËÆ¶È:60%
Phytochemistry          1994          36          1439-1442
Sesquiterpenes from Fabiana imbricata
Guillermo Schmeda-Hirschmann, Fani Papastergiou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     (+)-cis-14-Normuurol-5-en-4-one
    ÏàËÆ¶È:60%
Phytochemistry          1994          36          961-965
cis-calamenene-related sesquiterpenoids from Cupressus bakeri foliage
Kim Young-Kyoon, Laurence G. Cool, Eugene Zavarin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     compound 12
    ÏàËÆ¶È:60%
Phytochemistry          1994          37          1101-1107
Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species
J.Alberto Marco, Juan F. Sanz-Cervera, Vicente Garcia-Lliso, Alfonso Susanna, Nuria Garcia-Jacas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 2
    ÏàËÆ¶È:60%
Tetrahedron Letters          2000          41          9219-9222
Synthesis and reactions of a novel chlorostannane resin: coupling with functionalized organozinc halides
Xizhen Zhu, Bruce E. Blough, F. Ivy Carroll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     ¦Á-Humulen-14-oic acid
    ÏàËÆ¶È:60%
Phytochemistry          1982          21          685-689
¦Á-Humulene derivatives including a sesquiterpene acid with a rearranged carbon skeleton from Lychophorora columnaris
Ferdinand Bohlmann, Christa Zdero, Harold Robinson, Robert M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     compound 2
    ÏàËÆ¶È:60%
Pharmazie          2002          57          59-61
Microbiological conversion of a - and -eudesmol mixture by Rhizopus
G.T. Maatooq - J.J. Hoffmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     1S,4R,6R-1,4-endoperoxy-bisabola-2,10-diene
    ÏàËÆ¶È:60%
Archives of Pharmacal Research          2000          23          151-154
Cytotoxic peroxides from Artemisia stolonifera
Hak Cheol Kwon, Sang Un Choi and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     5(10),13E-ent-halimadien-15,16-olide
C20H30O2     ÏàËÆ¶È:60%
Tetrahedron Letters          2003          44          369-372
Synthesis and absolute configuration of three natural ent-halimanolides with biological activity
I.S Marcos, A.B Pedrero, M.J Sexmero, D Diez, P Basabe, F.A Hern¨¢ndez, J.G Urones
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     (1R,7S,10S)-7-(1-Methylethyl)-10-methylbicyclo[4.4.0]dec-5-en-4-one
    ÏàËÆ¶È:60%
Journal of the Chemical Society, Perkin Transactions 1          2000                   189-194
Synthesis of sesquiterpene allylic alcohols and sesquiterpene dienes from Cupressus bakeri and Chamaecyparis obtusa
Koon-Sin Ngo and Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     compound 3a
C14H24O2     ÏàËÆ¶È:60%
Tetrahedron          2002          58          1647-1656
Studies on the synthesis of (¡À)-pathylactone A, a nor-sesquiterpene lactone isolated from marine sources
Fernando Coelho, Gaspar Diaz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     4-keto-15-nor-muurol-5-ene
C14H22O     ÏàËÆ¶È:60%
Tetrahedron          1999          55          15109-15126
Autoxidation of 4-amorphen-11-ol and the biogenesis of nor- and seco-amorphane sesquiterpenes from fabiana imbricata
Koon-Sin Ngo, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     exo,exo-8-methyltetracyclo[4.4.(12,5).(17,10).0(1,6)]-dodec-exo-3(4)-yl acetate
C15H22O2     ÏàËÆ¶È:60%
Russian Journal of Organic Chemistry          2005          41          974-977
Synthesis of Esters from Cage-Like Unsaturated Hydrocarbons, Carboxylic Acid Anhydrides, and Water
M. K. Mamedov, E. K. Nabieva and R. A. Rasulova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     ¦Ã-eudesmol
    ÏàËÆ¶È:60%
Zeitschrift f¨¹r Naturforschung C          2002          57          654-659
Microbial Transformation of a b- and g-Eudesmols Mixture
G. T. Maatooq
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     (-)-nor-aromadendr-10¦Â-ol
    ÏàËÆ¶È:60%
Zeitschrift f¨¹r Naturforschung C          2009          64          840-846
Structure-Activity Relationships of Aromadendranes in Uterus-Relaxant Activity
N. P¨¦rez-Hern¨¢ndez, H. Ponce-Monter, M. I. Ortiz, R. Cariño-Cort¨¦sa, and P. Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     compound 9
    ÏàËÆ¶È:60%
Canadian Journal of Chemistry          1986          64          1-4
Stress metabolites of Solanummelongena: biosynthetic studies and isolation of auberganol and ¦Á- and ¦Â-eudesmol
Albert Stoessl, J.B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     costic acid
    ÏàËÆ¶È:60%
Phytochemistry          2013          95          19-93
Sesquiterpenoids in subtribe Centaureinae (Cass.) Dumort (tribe Cardueae, Asteraceae): Distribution, 13C NMR spectral data and biological properties Review Article
Maurizio Bruno, Svetlana Bancheva, Sergio Rosselli, Antonella Maggio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     Isolongifolene Alcohol
    ÏàËÆ¶È:60%
Journal of Agricultural and Food Chemistry          1994          42          138-142
Structure elucidation of oxidation-reduction products of isolongifolene
Isabelle Bombarda, Jacqueline Smadja, Emile M. Gaydou, Jacques Yves Conan, Robert Faure
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     (-)-epi-cedrol
C15H26O     ÏàËÆ¶È:60%
Journal of Agricultural and Food Chemistry          2012          60          124-128
Phytochemicals from Cunninghamia konishii Hayata Act as Antifungal Agents
Sen-Sung Cheng, Min-Jay Chung, Chun-Ya Lin, Ya-Nan Wang, and Shang-Tzen Chang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     (6S,7R)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one
    ÏàËÆ¶È:60%
European Journal of Organic Chemistry          1998          1998          2851-2854
Synthesis of (6S,7S)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the Opposite Enantiomer of the Antibacterial Sesquiterpene from Premnaoligotricha, and the (R) Enantiomer of Ancistrodial, the Defensive Sesquiterpene from Ancistrotermes cavithorax
Sayo Horiuchi, Hirosato Takikawa and Kenji Mori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     (6R*,7S *)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one
C15H26O2     ÏàËÆ¶È:60%
European Journal of Organic Chemistry          1996          1996          891-897
Synthesis of Mono- and Sesquiterpenoids, XXV. Synthesis of (6R*,7R*)-7-Hydroxy-6,11-cyclofarnes-3(15)-en-2-one, the Racemate of the Antibacterial Sesquiterpene from Premna oligotricha, and Its (6R*,7S*) Isomer
Arata Yajima, Hirosato Takikawa and Kenji Mori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     14-chloroxeniaphylla-4,8(19)-dien-15-ol
C20H33ClO     ÏàËÆ¶È:60%
Australian Journal of Chemistry          1981          34          2657-2664
Studies of Australian soft corals. XXV. Several caryophyllene-based diterpenes from a Nephthea species
A Ahond, BF Bowden, JC Coll, J Fourneron and SJ Mitchell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     5,10-dehydroambliol B
    ÏàËÆ¶È:60%
The Journal of Organic Chemistry          1988          53          4574-4578
Sesterterpene sulfates from a sponge of the family Halichondriidae
Michael R. Kernan, D. John Faulkner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     ¦Ã-Eudesmol
    ÏàËÆ¶È:60%
Magnetic Resonance in Chemistry          1995          33          233-235
Two-dimensional NMR of sesquiterpenes. 8¡ªcomplete assignment of 1H and 13C NMR spectra of seven sequiterpene alcohols from Neocallitropsis pancheri
Phila Raharivelomanana, Jean-Pierre Bianchini, Aim¨¦ Cambon, Marcel Azzaro and Robert Faure
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     (6¦Á,8¦Á)-6-acetyloxy)eremophil- 7(11)-en-12,8-olide
C17H24O4     ÏàËÆ¶È:58.8%
Helvetica Chimica Acta          2006          Vol. 89          915
Terpenoids from the Roots of Ligularia muliensis
Qiu-Hong Wu, Chun-Mei Liu, Yan-Jun Chen, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     compound 11
C21H28O4     ÏàËÆ¶È:58.8%
Journal of Natural Products          2003          66          1263-1265
Determination of the Absolute Stereochemistry of Cyclosmenospongine
Natalia K.Utkina,Vladimir A. Denisenko, Olga V. Scholokova, and Aleksandra E. Makarchenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     (2R,3R)-2-Hydroxy-3-(hydroxymethyl)-3,5-dimethyl-N-(3-oxo-3-(pentylamino)propyl)hexanamide
C17H34N2O4     ÏàËÆ¶È:58.8%
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
59 .     nardosinanol D
C16H26O4     ÏàËÆ¶È:56.2%
Journal of Natural Products          2008          71(3)          375-380
Nardosinanols A#I and Lemnafricanol, Sesquiterpenes from Several Soft Corals, Lemnalia sp., Paralemnalia clavata, Lemnalia africana, and Rhytisma fulvum fulvum
Ashgan Bishara, Dina Yeffet, Mor Sisso, Guy Shmul, Michael Schleyer, Yehuda Benayahu, Amira Rudi, and Yoel Kashman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     3¦Á,4¦Á-Isopropyliden-¦Â-ionol
C16H26O3     ÏàËÆ¶È:56.2%
Journal of Asian Natural Products Research          2005          7          151-156
Three new compounds from Isodon melissoides
AI-HUA ZHAO, RONG-TAO LI, BEI JIANG, JI-XIA ZHANG,QIN-SHI ZHAO and HAN-DONG SUN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     1-naphthalene acetic-7-oxo-1,2,3,4,4a,7,8,8a-octahydro-1,2,4a,5-tetramethyl acid
C16H24O3     ÏàËÆ¶È:56.2%
Phytochemistry          1992          31          1823-1825
Tetranorditerpenes from Detarium microcarpum
Rita Aquino, Maria Letizia Ciavatta, Nunziatina De Tommasi, Eszter G¨¤cs-Baitz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     norambreinolide-18,6¦Á-olide
C16H22O4     ÏàËÆ¶È:56.2%
Journal of Natural Products          2010          73          1601-1605
Sesterterpenoids and Other Constituents of Salvia sahendica
Firouz Matloubi Moghaddam, Mahdi Moridi Farimani, Marjan Seirafi, Salman Taheri, Hamid Reza Khavasi, Jandirk Sendker, Peter Proksch, Victor Wray, and RuAngelie Edrada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     flavalin E
C16H24O3     ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          2011          59(6)          698-702
Sesquiterpenoids from the Formosan Soft Coral Lemnalia flava
Jui-Hsin SU, Yi LU, Wen-Yu HUNG,Chiung-Yao HUANG, Michael Y. CHIANG,Ping-Jyun SUNG, Yao-Haur KUO,and Jyh-Horng SHEU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     paralemnolin P
C16H24O3     ÏàËÆ¶È:56.2%
Chemical & Pharmaceutical Bulletin          2010          58          30-33
Paralemnolins J¡ªP, New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoide
Guey-Horng Wang, Ho-Cheng Huang, Jui-Hsin Su, Yang-Chang Wu and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     1¦Â-t-butoxy-4-(3'-oxobutyl)-7a¦Â-methyl-7,7a-dihydro-5(6H)-indanone
    ÏàËÆ¶È:56.2%
Steroids          1984          44          283-292
[1,2,3,4-13C] Testosterone and [1,2,3,4-13C] estradiol
Gijsbert Zomer, Hans Wynberg, Nick M. Drayer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     compound 11a
    ÏàËÆ¶È:56.2%
Tetrahedron Letters          2004          45          6017-6020
A new approach to the synthesis of polycyclic structures
Michael E Briggs, Myriem El Qacemi, Chakib Kalaı̈, Samir Z Zard
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     DL-N-[5-(p-Amidinophenyl)pentanoyl]-3-methyl-¦Â-alanineethylester
C18H27N3O3     ÏàËÆ¶È:56.2%
Bioorganic & Medicinal Chemistry          1995          3          539-551
A novel series of orally active antiplatelet agents
Jeffery A. Zablocki, Foe S. Tjoeng, Philippe R. Bovy, Masateru Miyano, Robert B. Garland, Kenneth Williams, Lori Schretzman, Mark E. Zupec, Joseph G. Rico, Richard J. Lindmark, Mihaly V. Toth, Dudley E. McMackins, Steven P. Adams, Susan G. Panzer-Knodle,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     [15-(13)C2H3]-E-7,11-Dehydro-dihydroartemisinic acid methyl ester
C16H24O2     ÏàËÆ¶È:56.2%
Tetrahedron          2007          63          9548-9566
In vivo transformations of artemisinic acid in Artemisia annua plants
Geoffrey D. Brown, Lai-King Sy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     tessaric acid methyl esthe[rmethyl 2-((2R,8S,8aR)-8,8a-dimethyl-6-oxo-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl)acrylate]
C16H24O2     ÏàËÆ¶È:56.2%
Bioorganic & Medicinal Chemistry          2009          17          6251-6256
Tessaric acid derivatives induce G2/M cell cycle arrest in human solid tumor cell lines
Leticia G. Le¨®n, Osvaldo J. Donadel, Carlos E. Tonn, Jos¨¦ M. Padr¨®n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     (3a'S,4'R,6a'R)-5,5-dimethyl-4'-(3-methylbut-2-enyl)-tetrahydro-1'H-spiro[[1,3]dioxane-2,2'-pentalen]-5'(3'H)-one
C18H28O3     ÏàËÆ¶È:56.2%
European Journal of Organic Chemistry          2010                   1149-1157
Synthesis of Functionalized Hydropentalenes by an Asymmetric Deprotonation/Alkylation Strategy
Vanessa Lutz, Angelika Baro, Peter Fischer and Sabine Laschat
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     13,19-dihydroxy-halima-5(10),14-diene
C20H34O2     ÏàËÆ¶È:55.5%
Biochemical Systematics and Ecology          2004          32          45-53
Diterpenes from Stevia gilliesii
Tamara L. Meragelman, Diego S. Pedrosa, Roberto R. Gil
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
72 .     19-nortestosterone
    ÏàËÆ¶È:55.5%
Steroids          2005          70          193-198
Steroids¡¯ transformations in Penicillium notatum culture
Agnieszka Bartma¨½ska, Jadwiga Dmochowska-Gładysz, Ewa Huszcza
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
73 .     Solajiangxin E
C18H28O3     ÏàËÆ¶È:55.5%
Phytochemistry Letters          2013          6          453-456
Three new cytotoxic sesquiterpenoids from Solanum lyratum
Fang Yao, Qin-Lan Song, Lei Zhang, Gui-Sheng Li, Sheng-Jun Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
74 .     2-Hydroxysolajiangxin E
C18H28O4     ÏàËÆ¶È:55.5%
Phytochemistry Letters          2013          6          453-456
Three new cytotoxic sesquiterpenoids from Solanum lyratum
Fang Yao, Qin-Lan Song, Lei Zhang, Gui-Sheng Li, Sheng-Jun Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
75 .     (-)-Perhydro-3¦Á,4a¦Á,7,7,10a¦Â-pentamethyl-cis-4a-transoid-10a,10b-trans-6a-naphtho[2,1-b]pyran
    ÏàËÆ¶È:55.5%
Helvetica Chimica Acta          1986          69          163-173
Conformation-Odor Relationships in Norlabdane Oxides
G¨¹nther Ohloff, Christian Vial, Edouard Demole, Paul Enggist, Wolfgang Giersch, Elise J¨¦gou, Andrew J. Caruso, Judith Polonsky and Edgar Lederer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
76 .     manaarenolide F
C20H32O6     ÏàËÆ¶È:55%
Journal of Natural Products          2006          69(8)          1134-1139
Manaarenolides A−I, Diterpenoids from the Soft Coral Sinularia manaarensis
Jui-Hsin Su, Atallah F. Ahmed, Ping-Jyun Sung, Chih-Hua Chao, Yao-Haur Kuo, and Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
77 .     (6¦Â)-5(R)-[2-(3-Furanyl)ethyl]-1,1,5,6-tetramethyl-1,2,3,4,5,6,7,8-octahydronaphthalene
C20H30O     ÏàËÆ¶È:55%
Journal of Natural Products          2000          63          1623-1625
Synthesis of 16,18-Dihydroxycleroda-3,13Z-dien-16,15-olide,(+)-16-Hydroxycleroda-3,13Z-dien-16,15-olide, and (-)-Hydroxyhalima-5(10),13-dien-16,15-olide from (+)-Hardwickiic Acid
Paulo M. Imamura, and Marta Costa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
78 .     Sapinsignoid E
C20H34O3     ÏàËÆ¶È:55%
Journal of Natural Products          2012          75          722-727
Cytotoxic Diterpenoids from Sapium insigne
Hong-Bing Liu, Hua Zhang, Jin-Hai Yu, Cheng-Hui Xu, Jian Ding, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
79 .     mixture of 2-bromo-2c-isobutyryl-3,3-dimethylcyclopropyl-1r-methanol and 1-bromo-2-isopropyl-6,6-dimethyl-3-oxabicyclo[3.1.0]hexan-2-ol
C10H18BrO2     ÏàËÆ¶È:55%
Russian Journal of Organic Chemistry          2005          41          1601-1609
Synthesis of 1-Bromosubstituted Analogs of cis-Deltamethrinic and cis-Permethrinic Acids
A. E. Sheshenev, M. S. Baird and I. G. Bolesov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
80 .     15-chloroxeniaphylla-4,8(19)-dien-14-ol
C20H33ClO     ÏàËÆ¶È:55%
Australian Journal of Chemistry          1981          34          2657-2664
Studies of Australian soft corals. XXV. Several caryophyllene-based diterpenes from a Nephthea species
A Ahond, BF Bowden, JC Coll, J Fourneron and SJ Mitchell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
81 .     xeniaphylla-4,8(19)-diene-14,15-diol
C20H34O2     ÏàËÆ¶È:55%
Australian Journal of Chemistry          1981          34          2657-2664
Studies of Australian soft corals. XXV. Several caryophyllene-based diterpenes from a Nephthea species
A Ahond, BF Bowden, JC Coll, J Fourneron and SJ Mitchell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
82 .     (-)-bicyclogermacrene
    ÏàËÆ¶È:53.3%
Chemistry & Biodiversity          2008          Vol. 5          2449
Furanocembranoids from the Soft Corals Sinularia asterolobata and Litophyton arboreum
Daniela Grote, Hans-Martin Dahse, and Karlheinz Seifert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
83 .     15-Hydroxy-Tmuurolol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2009          72          99-101
T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes
Ling Ding, Roland Pfoh, Stephan Ruhl, Song Qin,and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
84 .     T-Muurolol
C15H26O     ÏàËÆ¶È:53.3%
Journal of Natural Products          2009          72          99-101
T-Muurolol Sesquiterpenes from the Marine Streptomyces sp. M491 and Revision of the Configuration of Previously Reported Amorphanes
Ling Ding, Roland Pfoh, Stephan Ruhl, Song Qin,and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
85 .     eremophil-6-en-11-ol
C15H26O     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2008          Vol. 91          1712
Two New Eremophilane-Type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana (Hemsl.) Greenm
Cai-FangWang, Yu Zhao, Yan-Ze Liu, and Zhen-Zhong Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
86 .     (6¦Á,8¦Á)-6-hydroxyeremophil-7(11)-en-12,8-olide
C15H22O3     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2006          Vol. 89          915
Terpenoids from the Roots of Ligularia muliensis
Qiu-Hong Wu, Chun-Mei Liu, Yan-Jun Chen, and Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
87 .     (3¦Â)-eudesm-4(14)-ene-3,11-diol
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2004          Vol. 87          1446
Eudesmane-Type Sesquiterpene Derivatives from Saussurea conica
Cheng-Qi Fan, Zha-Jun Zhan, Hui Li, and Jian-Min Yue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
88 .     Isom¨¦re cis(1S,3S,4S,6S)
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2001          Vol. 84          2430
Epoxyesters p-menthaniques et pinaniques en milieu basique -Parfum de noix de coco
Marie-Jos¨¦phe Bourgeois et Evelyne Montaudon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
89 .     Isom¨¦re trans (1R,3R,4R,6S)
    ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2001          Vol. 84          2430
Epoxyesters p-menthaniques et pinaniques en milieu basique -Parfum de noix de coco
Marie-Jos¨¦phe Bourgeois et Evelyne Montaudon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
90 .     elongatol A
C15H24O3     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2007          55(5)          762-765
Nardosinane Sesquiterpenoids from the Formosan Soft Coral Nephthea elongata
Shang-Kwei WANGa and Chang-Yih DUH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
91 .     15-hydroxyallo-cedrol
C15H26O2     ÏàËÆ¶È:53.3%
Phytochemistry          2007          68          2409-2414
Sesquiterpenes from the wood of Juniperus lucayana
Yarelis Ort¨ªz Nuñez, Iraida Spengler Salabarria, Isidro G. Collado,Rosario Hern¨¢ndez-Gal¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
92 .     (-)-epi-cedrol
    ÏàËÆ¶È:53.3%
Phytochemistry          2003          64          303-323
Terpenoids from the seeds of Artemisia annua
Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
93 .     (-)-amorpha-4,7(11)-diene
    ÏàËÆ¶È:53.3%
Phytochemistry          2002          61          79-91
Volatile components from European liverworts Marsupella emarginata, M. aquatica and M. alpina
Adewale Martins Adio, Claudia Paua, Wilfried A. König, Hermann Muhle
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
94 .     (-)-lupanine
    ÏàËÆ¶È:53.3%
Phytochemistry          2002          61          975-978
Quinolizidine alkaloids from the curare adjuvant Clathrotropis glaucophylla
Anne-Lise Sagen, J¨¹rg Gertsch, Rita Becker, Jörg Heilmann, Otto Sticher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
95 .     illudiolone
C15H24O3     ÏàËÆ¶È:53.3%
Phytochemistry          2002          61          395-398
Sesquiterpenes from Omphalotus illudens
Trevor C. McMorris, A. Kashinatham, Ricardo Lira, Henrik Rundgren, Peter K. Gantzel,Michael J. Kelner, Robin Dawe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
96 .     compound 5
C15H24     ÏàËÆ¶È:53.3%
Phytochemistry          2001          58          969-972
ent-Daucane and acorane sesquiterpenes from¡ÁCupressocyparis leylandii foliage
Laurence G. Cool
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
97 .     halichonadin F
C15H27N     ÏàËÆ¶È:53.3%
Journal of Natural Products          2008          71(7)          1301-1303
Halichonadin F and the Cu(I) Complex of Halichonadin C from the Sponge Halichondria sp.
Haruaki Ishiyama, Shingo Kozawa, Kazuki Aoyama,Yuzuru Mikami, Jane Fromont, and Jun¡¯ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
98 .     mairetolide F
C15H22O4     ÏàËÆ¶È:53.3%
Journal of Natural Products          2006          69          1471-1475
Eremophilanes from Senecio mairetianus and Some Reaction Products
Ana-L. Prez-Castorena, Amira Arciniegas, S. Laura Guzmn, Jos Luis Villaseor, and Alfonso Romo de Vivar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
99 .     (-)-(1R,7S,-10R)-1-hydroxy-11-norcadinan-5-en-4-one
C14H22O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          1309-1313
Norsesquiterpenes from the Brown Alga Dictyopteris divaricata
Fuhang Song, Xiuli Xu, Shuai Li, Sujuan Wang, Jielu Zhao, Peng Cao, Yongchun Yang, Xiao Fan, Jiangong Shi, Lan He, and Yang L
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
100 .     (4S,9S,10R)-4,10,11-tribromo-10,11-seco-lippifoli-1(6)-en-5-one
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2005          68          659-665
Absolute Configuration of Lippifoliane and Africanane Derivatives
Carlos M. Cerda-Garca-Rojas, Angelina del C. Coronel, Marina E.P. de Lampasona, Csar A. N. Cataln, and Pedro Joseph-Nathan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
101 .     5¦Á,7¦Á,10¦ÂH-3-patchoulen-2-one
C15H22O     ÏàËÆ¶È:53.3%
Journal of Natural Products          2004          67          914-917
Three New Sesquiterpenes from Croton arboreous
A. Berenice Aguilar-Guadarrama, and Mara Yolanda Rios
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
102 .     (4R,5S,6R,7R,11S)-12-Hydroxy-1(10)-aromadendren-14-al
C15H22O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2004          67          799-805
Isolation of a Library of Aromadendranes from Landolphia dulcis and Its Characterization Using the VolSurf Approach
Brian Skole, Flemming S. Jrgensen, Bogdan A. Budnik, Patrick Ekpe, and Jerzy W. Jaroszewski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
103 .     10¦Á,15-dihydroxyamorph-4-en-3-one
C15H24O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2007          70          304-306
Amorphane Sesquiterpenes from a Marine Streptomyces sp
Shao Jie Wu,Serge Fotso, Fuchao Li, Song Qin, and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
104 .     5¦Â,8¦Â-epidioxy-11-hydroxy-6-eudesmene
C15H24O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2007          70          1449-1453
Sesquiterpenoids and Artificial 19-Oxygenated Steroids from the Formosan Soft Coral Nephthea erecta
Shi-Yie Cheng,Chang-Feng Dai, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
105 .     8¦Â-hydroxyprespatane
C15H24O     ÏàËÆ¶È:53.3%
Journal of Natural Products          2007          70          1449-1453
Sesquiterpenoids and Artificial 19-Oxygenated Steroids from the Formosan Soft Coral Nephthea erecta
Shi-Yie Cheng,Chang-Feng Dai, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
106 .     8¦Â-hydroperoxyprespatane
C15H24O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2007          70          1449-1453
Sesquiterpenoids and Artificial 19-Oxygenated Steroids from the Formosan Soft Coral Nephthea erecta
Shi-Yie Cheng,Chang-Feng Dai, and Chang-Yih Duh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
107 .     compound 2
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          1319-1322
African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol
Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
108 .     compound 3
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2002          65          1319-1322
African Elephant Sesquiterpenes. II. Identification and Synthesis of New Derivatives of 2,3-Dihydrofarnesol
Thomas E. Goodwin,Felisia D. Brown, Richard W. Counts, Nichole C. Dowdy, Patrick L. Fraley,Randall A. Hughes, Daniel Z. Liu, Courtney D. Mashburn, Josh D. Rankin, Russell S. Roberson, Katie D. Wooley, Elizabeth L. Rasmussen, Scott W. Riddle, Heidi S. Ridd
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
109 .     (4S,5S,6¦Á,7¦Á,10R)-eudesma-5-en-11-ol epoxide
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          2001          64          393-395
Oxygenated Sesquiterpenoids from a Nonpoisonous Sardinian Chemotype of Giant Fennel (Ferula communis)
Giovanni Appendino, Giancarlo Cravotto, Olov Sterner, and Mauro Ballero
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
110 .     manshurolide
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          415-418
Sesquiterpene Esters of Aristolochic Acid from the Root and Stem of Aristolochia heterophylla
Tian-Shung Wu, Yu-Yi Chan, Yann-Lii Leu, and Zong-Tsi Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
111 .     2,6,10-trimethyl-2-undecen-6-ol
C14H28O     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          214-218
Nuapapuin A and Sigmosceptrellins D and E: New Norterpene Cyclic Peroxides from a Southern Australian Marine Sponge, Sigmosceptrella sp.
Simon P. B. Ovenden and Robert J. Capon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
112 .     1,10-seco-4¦Î -hydroxy-muurol-5-ene-1,10-diketone
C15H24O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          549-553
Muurolane Sesquiterpenes from Illicium tsangii
Koon-Sin Ngo, Wing-Tak Wong, and Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
113 .     dihydroartemisinic acid
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          430-433
Isolation and Identification of Dihydroartemisinic Acid from Artemisia annua and Its Possible Role in the Biosynthesis of Artemisinin
T. Eelco Wallaart, Wim van Uden, Heidi G. M. Lubberink, Herman J. Woerdenbag, Niesko Pras, and Wim J. Quax
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
114 .     (8R)-8-hydroxypatchoulol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          437-440
Biotransformation of the Fungistatic Sesquiterpenoid Patchoulol by Botrytis cinerea
Josefina Aleu, James R. Hanson, Rosario Hern¨¢ndez Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
115 .     triterpenoid
C30H50O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          653-654
A New Acyclic Diketotriterpenoid Isolated from the Indonesian Marine Sponge Hyrtios erectus
David E. Williams, Akbar Tahir, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
116 .     3-ketodihydroartemisinic acid
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          790-793
Semisynthesis of 3-¦Â-Hydroxyartemisinin
Nancy Acton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
117 .     compound 9
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          790-793
Semisynthesis of 3-¦Â-Hydroxyartemisinin
Nancy Acton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
118 .     7¦ÂH-eudesm-2-ene-4¦Á,11-diol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1998          61          22-28
Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol
Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
119 .     carissone
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1996          59          409-411
Constituents of Persea japonica
Chao-Chiun Wang, Chang-Sheng Kuoh and Tian-Shung Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
120 .     compound 2
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1996          59          866-868
Drimane Sesquiterpenes from the Sponge Dysidea fusca
A. Montagnac, M.-T. Martin, C. Debitus, and M. Païs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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