| ²é¿´: 475 | »Ø¸´: 1 | |||
WJY515Ìú³æ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóάÆÕ ÒÑÓÐ1È˲ÎÓë
|
|
Êý¾ÝÈçÏ£º 11.4,25.2,29.9,34.1, 34.9,35.4,39.7,42.7,74.8,123.3,130.2,138.7,158.8,169.9,198.0 |
» ²ÂÄãϲ»¶
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸211µç×ÓÐÅÏ¢347Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
²ÄÁÏÓ뻯¹¤300Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
0856ר˶Çóµ÷¼Á Ï£ÍûÊÇaÇøÔºÐ£
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
±¾¿ÆÎ÷¹¤´ó 0856 324Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
µ÷¼Á
ÒѾÓÐ8È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ19È˻ظ´
277 ÊýÒ»104£¬Ñ§Ë¶£¬Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48419.9
- ºì»¨: 52
- Ìû×Ó: 6747
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
WJY515: ½ð±Ò+5 2015-03-19 08:55:12
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
WJY515: ½ð±Ò+5 2015-03-19 08:55:12
|
1 . (+)-3-oxodiplophyllin C15H18O3 ÏàËÆ¶È:100% Phytochemistry 1985 24 1199-1201 Ant-repellent sesquiterpene lactones from Eupatorium quadrangularae Adewole L. Okunade, David F. Wiemer Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (3¦ÁR,8¦ÁR,9¦ÁR)-5,8¦Á-dimethyl-3-methylene-3¦Á,4,8,8¦Á,9,9¦Á-hexahydronaphtho[2,3-¦Â]furan-2,6(3H,7H)-dione C15H18O3 ÏàËÆ¶È:100% Natural Product Research and Development 2010 22 736-739 Sesquiterpenoids from Tibetan Folk Drug Pulicaria insignis HUANG Sheng-zhuo;JIANG Si-ping; ZHU Hua-jie Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-oxo-4(5),11-eudesmadien-8,12-olide C15H18O3 ÏàËÆ¶È:100% Chemistry of Natural Compounds 2012 48 416-418 A new triterpenoid ester from Lobelia sessilifolia Jiaming Sun, Xiuli Wang, Hui Zhang and Junshan Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-(2-(methoxycarbonylamino)ethyl)-1-methyl-1H-imidazol-3-ium C19H23N4O4 ÏàËÆ¶È:60% Organic Letters 2008 Vol.10,No.19 4247-4250 Bistellettazines A-C and Bistellettazole A: New Terpenyl-Pyrrolizidine and Terpenyl-Imidazole Alkaloids from a Southern Australian Marine Sponge,Stelletta sp Mohamed El-Naggar, Andrew M. Piggott, and Robert J. Capon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-Oxo-di-nor-eudesma-4-en-11-oic acid C13H18O3 ÏàËÆ¶È:60% Phytochemistry 2013 96 201-207 Eudesmane-type sesquiterpene derivatives from Laggera alata Guo-Cai Wang, Guo-Qiang Li, Hua-Wei Geng, Tao Li, Jiao-Jiao Xu, Fang Ma, Xia Wu, Wen-Cai Ye, Yao-Lan Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (3aR,4aS,5aR,6aR)-octahydro-5-[(3E)-3-(hydroxyimino)butyl]-5a-methyl-3-methylidene-2H-cyclopropa[f][1]benzofuran-2-one C15H21NO3 ÏàËÆ¶È:60% Chemistry & Biodiversity 2014 11 886-903 Semisynthesis and Antifungal Activity of Novel Oxime Ester Derivatives of Carabrone Modified at C(4) against Botrytis cinerea Delong Wang, Shuangxi Ren, Hao Wang, He Yan, Juntao Feng and Xing Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . fascicularone I C15H22O5 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2005 Vol. 88 2944 Fascicularones H¨CK, Four New Sesquiterpenoids from the Cultured Mycelia of the Fungus Hypholoma fasciculare Hironari Akasaka, Yoshihito Shiono, Tetsuya Murayama, and Michimasa Ikeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 1¦Â,4¦Â-epoxy-5¦Â-hydroxy-10¦ÁH-xantha-11(13)-en-12,8¦Â-olide C15H22O4 ÏàËÆ¶È:53.3% Journal of Natural Products 2003 66 1554-1557 Xanthanolides, Germacranolides, and Other Constituents from Carpesium longifolium Chao Yang, Chengshan Yuan, and Zhongjian Jia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 1¦Á,4¦Á-epoxy-5¦Á-hydroxy-10¦ÂH-xantha-11(13)-en-12,8¦Á-olide C15H22O4 ÏàËÆ¶È:53.3% Chinese Chemical Letters 2003 14 483-484 A New Xanthanolide from Carpesium longifolium Chao YANG, Meng Chun YE, Zhong Jian JIA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . yomogin ÏàËÆ¶È:53.3% Phytochemistry 1988 27 1113-1120 Lumiyomogin,ferreyrantholide,fruticolide and other sesquiterpene lactones from Ferreyranthus fruticosus J. Jakupovic,A. Schuster,F. Bohlmann,M.O. Dillon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 1¦Á,2¦Á-epoxy-3¦Á-hydroxyeudesm-4-ene-12,8¦Â-olide C15H18O4 ÏàËÆ¶È:53.3% Phytochemistry 1988 27 1113-1120 Lumiyomogin,ferreyrantholide,fruticolide and other sesquiterpene lactones from Ferreyranthus fruticosus J. Jakupovic,A. Schuster,F. Bohlmann,M.O. Dillon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . dendocarbin-A C15H24O2 ÏàËÆ¶È:53.3% Tetrahedron 2005 61 11032-11037 Pelseneeriol-1 and -2: new furanosesquiterpene alcohols from porostome nudibranch Doriopsilla pelseneeri Helena Gaspar, Margherita Gavagnin, Gonçalo Calado, Francesco Castelluccio, Ernesto Mollo, Guido Cimino Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 9¦Â-hydroxy-3-oxo-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 Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 4-hydroxy-1¦Â,5¦Â-epoxy-10¦ÁH-xantha-11(13)-en-12,8¦Â-olide C15H22O4 ÏàËÆ¶È:53.3% European Journal of Medicinal Chemistry 2011 46 5408-5415 Sesquiterpene lactones from Inula falconeri, a plant endemic to the Himalayas, as potential anti-inflammatory agents Xiangrong Cheng, Qi Zeng, Jie Ren, Jiangjiang Qin, Shoude Zhang, Yunheng Shen, Jiaxian Zhu, Fei Zhang, Ruijie Chang, Yan Zhu, Weidong Zhang, Huizi Jin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 4-(5-ethoxycarbonyl-pentanoyl)-3,5-dimethyl-1H-pyrrole-2-carboxylic acid ÏàËÆ¶È:53.3% Journal of Medicinal Chemistry 2007 50 1528-1536 Synthesis and Anti-Cancer Activity of C-Ring-Functionalized Prodigiosin Analogues Jasmine Regourd, Adeeb Al-Sheikh Ali, and Alison Thompson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (6R,7E,10R)-6-{[(tert-Butyl)dimethylsilyl]oxy}-3,4,5,6,9,10-hexahydro-10-methyl-2H-oxecin-2-one C16H30O3Si ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2011 94 224-229 An Iterative Acetylene¨CEpoxide Coupling Strategy for the Total Synthesis of Aspinolide A Gowravaram Sabitha, Teega Rammohan Reddy, Chitti Srinivas and Jhillu Singh Yadav Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-18 22:52:24













»Ø¸´´ËÂ¥