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jessiegao07

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13C NMR
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1 .     Euphoractine B
C29H38O6     ÏàËÆ¶È:70.3%
Phytochemistry          1993          32          208-210
Diterpenoids from Euphorbia micractina
Jian-Gong Shi, Zhong-Jian Jia, Li Yang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     euphoractin I
C29H40O6     ÏàËÆ¶È:65.5%
Journal of Natural Products          2013          76          1039-1046
Diterpenoids with Diverse Skeletons from the Roots of Euphorbia micractina
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Ying Guo, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 43
C36H50O4Si     ÏàËÆ¶È:64%
The Journal of Organic Chemistry          1998          63          306-313
Total Synthesis of Allocyathin B2, a Metabolite of Bird's Nest Fungi
Motoo Tori, Naoko Toyoda, and Masakazu Sono
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (22E,24R)-3¦Â-ôÇ»ùÂó½ÇçÞ-5,8,22-ÈýÏ©-7-ͪ
C28H42O2     ÏàËÆ¶È:60.7%
Journal of Chinese Medicinal Materials          2008          31          1343-1347
Studies on the Anti-tumor Activity Principles of a Marine-derived Fungus BZYT-21
GAO Zong-hua, MA Li-ying, SHEN Yun-xiu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     3¦Â,5¦Á,9¦Á-ÈýôÇ»ù-(22E,24R)-Âó½ÇçÞ-7,22-¶þÏ©-6-ͪ
    ÏàËÆ¶È:60.7%
Journal of Tropical and Subtropical Botany          2011          19          75-78
Steroidal Metabolites of Fimetariella rabenhorstii,Endophytic Fungus from Aquilaria sinensis
TAO, Meihua, YAN, Jian, WEI, Xiaoyi, LI, Dongli, ZHANG, Weimin, TAN, Jianwen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     scuterivulactone A
C29H36O8     ÏàËÆ¶È:59.2%
Chemical & Pharmaceutical Bulletin          1997          45          152-160
Studies on the Constituents of Scutellaria Species. XVIII. Structures of Neoclerodane-Type Diterpenoids from the Whole Herb of Scutellaria rivularis WALL.
Haruhisa KIZU,Yoshitaka IMOTO,Tsuyoshi TOMIMORI,Tohru KIKUCHI,Shigetoshi KADOTA and Koji TSUBONO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     euphoractin F
C27H36O6     ÏàËÆ¶È:59.2%
Journal of Natural Products          2013          76          1039-1046
Diterpenoids with Diverse Skeletons from the Roots of Euphorbia micractina
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Ying Guo, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     1,4,6-Cholestatrien-3¦Á-ol
    ÏàËÆ¶È:57.6%
Steroids          2007          72          360-367
Chemoselective reduction of 1,4,6-cholestatrien-3-one and 1,4,6-androstatriene-3,17-dione by various hydride reagents
Eunjeong Kim, Eunsook Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 12
    ÏàËÆ¶È:57.1%
Steroids          1995          60          666-673
New cytotoxic steroids from the marine sponge Dysidea fragilis coming from the lagoon of Venice
Anna Aiello, Ernesto Fattorusso, Marialuisa Menna, Rosa Carnuccio, Teresa Iuvone
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (22E,24R)-ergosta-7,22-dien-3¦Â,5¦Á,9¦Á-trihydroxy-6-one
C28H44O4     ÏàËÆ¶È:57.1%
Natural Product Research and Development          2007          19          436-438
Chemical Constituents of Basidiomycetes Russula subnigricans
GONG Qing-fang; ZHANG Yu-mei; TAN Ning-hua; CHEN Zuo-hong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 3
C30H40O7     ÏàËÆ¶È:57.1%
Tetrahedron          2004          60          5025-5030
New tri- and tetracyclic diterpenes from Euphorbia villosa
Andrea Vasas, Judit Hohmann, Peter Forgo, P¨¢l Szab¨®
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     euphoractin H
C28H38O6     ÏàËÆ¶È:57.1%
Journal of Natural Products          2013          76          1039-1046
Diterpenoids with Diverse Skeletons from the Roots of Euphorbia micractina
Ye Tian, Wendong Xu, Chenggen Zhu, Sheng Lin, Ying Guo, and Jiangong Shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3¦Â,5¦Á,9¦Á-trihydroxyl-(22E,24R)-ergosta-7,22-diene-6-one
    ÏàËÆ¶È:57.1%
Natural Product Research and Development          2012          24          1047-1050
Secondary Metabolites from Marine Fungus Fusarium sp.
LIU Tao; LI Zhan-lin; WANG Yu; TIAN Li; PEI Yue-hu; HUA Hui-ming
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3¦Â,5¦Á,9¦Á-trihydroxyergosta-7,22-dien-6-one
    ÏàËÆ¶È:57.1%
Natural Product Research and Development          2012          24          1747-1749
Chemical Constituents of Favolus arcularius
YIN Wei, LIU Jin-song, WU Pei-yun, LIANG Yi-min, WANG Gang*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (13R)-8¦Â,13-epoxyclerodane
C34H38O7     ÏàËÆ¶È:56.6%
Journal of Natural Products          1998          61          1030-1032
Some Biogenetic-Type Transformations of Neoclerodane Diterpenoids from Scutellaria Species
Ahmed A. Hussein, Dulce M. Muñ oz, Mar¨ªa C. de la Torre, and Benjam¨ªn Rodr¨ªguez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     2-[(4¦ÂS,8aS)-3,4b,5,6,7,8,8a,9-Octahydro-4-hydroxy-1,4b,8,8-tetramethyl-3,9-dioxophenanthren-2-yl]ethyl 4-¦ÂRomobenzoate
    ÏàËÆ¶È:56%
Helvetica Chimica Acta          2000          Vol. 83          407
A New Potent Antifungal Quinone Methide Diterpene with a Cassane Skeleton from Bobgunnia madagascariensis
Fr¨¦d¨¦ ric Schaller, Lila Rahalison, Nurul Islam, Olivier Potterat, and Kurt Hostettmann,Helen Stoeckli-Evans,Steven Mavi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     scopadulcic acid C
C27H36O5     ÏàËÆ¶È:56%
Chemical & Pharmaceutical Bulletin          2006          54(4)          546-549
Chemical and Biological Evaluation on Scopadulane-Type Diterpenoids from Scoparia dulcis of Vietnamese Origin
PHAN Minh Giang,PHAN Tong Son,Katsuyoshi MATSUNAMI,and Hideaki OTSUKA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     eufoboetol
    ÏàËÆ¶È:56%
Phytochemistry          1999          51          439-444
Steroids and a tetracyclic diterpene from Euphorbia boetica
Maria-Jose U. Ferreira, Jose R. Ascenso
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     8-¦Á-benzoyloxyspathulenol
    ÏàËÆ¶È:56%
Phytochemistry          1990          29          881-886
Sesquiterpene aryl esters from Ferulago antiochia
Mahmut Miski,Hani A. Moubasher,Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Tobeastriver
2Â¥2013-08-28 10:46:57
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