| ²é¿´: 207 | »Ø¸´: 1 | ||
jessiegao07½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬Ð»Ð»
|
|
13C NMR ÈܼÁ£ºCDCl3 13.01,16.70,19.44,19.95,20.60,21.82,27.20,28.61,29.16,34.09,41.54,42.90,46.97,52.52,62.71,63.65,75.85,80.50,87.81,128.63,129.76,131.11,132.98,165.01,207.07 ·Ç³£¸Ðл£¡ |
» ²ÂÄãϲ»¶
»úе¹¤³Ì264ѧ˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
±ÏÒµ¼±ÐèÊý¾Ý£¬Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
danil1288
½ð³æ (ÕýʽдÊÖ)
- Ó¦Öú: 96 (³õÖÐÉú)
- ½ð±Ò: 4099.5
- É¢½ð: 14
- ºì»¨: 2
- Ìû×Ó: 405
- ÔÚÏß: 109.3Сʱ
- ³æºÅ: 779961
- ×¢²á: 2009-05-26
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©Ò©ÐÔÀíÂÛ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jessiegao07: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£·Ç³£¸Ðл£¡ 2013-08-28 12:05:52
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jessiegao07: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ·Ç³£·Ç³£¸Ðл£¡ 2013-08-28 12:05:52
|
²éѯ½á¹û£º¹²²éµ½170¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

2Â¥2013-08-28 10:46:57














»Ø¸´´ËÂ¥