| ²é¿´: 232 | »Ø¸´: 1 | ||
lx33103310¾èÖú¹ó±ö (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö,Ê®·Ö¸Ðл£¡ ÒÑÓÐ1È˲ÎÓë
|
|
cÆ×ÈçÏ£¬ 18.2,22.5,22.7,24.2,24.8,27.1,28.6,38.8,40.2,70.0,73.2,76.6,78.7,110.3,118.4,122.6,135.3,145.4,154.8. Ê®·Ö¸Ðл£¡ [ ·¢×ÔÊÖ»ú°æ http://muchong.com/3g ] |
» ²ÂÄãϲ»¶
µçÆø×¨Ë¶320Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸Î÷±±¹¤Òµ´óѧ289 085602
ÒѾÓÐ33È˻ظ´
Ò»Ö¾Ô¸¹þ¹¤´ó 085600 277 12²Ä¿Æ»ùÇóµ÷¼Á
ÒѾÓÐ24È˻ظ´
268·Ö085602»¯Ñ§¹¤³Ìµ÷¼Á
ÒѾÓÐ28È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ50È˻ظ´
Çóµ÷¼Á£¬262»úеר˶
ÒѾÓÐ8È˻ظ´
305Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
347Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
272·Ö²ÄÁÏ×ÓÇóµ÷¼Á
ÒѾÓÐ47È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¡¸Ð¼¤£¡
ÒѾÓÐ3È˻ظ´
·Ç³£¸Ðл£¡Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬¿É·ñÓÐÈËÖ¸µã»òÔõÑù²éµ½´øÓÐÒÑÖªµ¥ÌåµÄºË´ÅÆ×Êý¾ÝÎÄÏ×
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾ÝÒ»¸ö!
ÒѾÓÐ5È˻ظ´
ÔÚÄĸöÍøÕ¾¿ÉÒԲ鵽»¯ºÏÎïµÄͼÆ×
ÒѾÓÐ3È˻ظ´
biosynthesis ºÍTotal synthesisµÄÇø±ð
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻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»
ÒѾÓÐ5È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- 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 ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lx33103310: ½ð±Ò+15, Õæ¿ì£¡ 2015-03-20 16:59:07
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
lx33103310: ½ð±Ò+15, Õæ¿ì£¡ 2015-03-20 16:59:07
|
1 . compound 4 C20H34O3 ÏàËÆ¶È:65% Tetrahedron 1993 49 515-524 New cembradiene diterpenoids from an undescribed Caribbean gorgonian of the genus Eunicea Jongheon Shin, William Fenical, Thomas J. Stout, Jon Clardy Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 6¦Á-Hydroxycyclonerolidol C15H26O2 ÏàËÆ¶È:63.1% Chemistry & Biodiversity 2012 9 727-738 Chemical Diversity of Essential Oils from Asteriscus graveolens (Forssk.)Less.:Identification of cis-8-Acetoxychrysanthenyl Acetate as a New Natural Component Gregory Cristofari,Mohamed Znini,Lhou Majidi,Hamid Mazouz,Pierre Tomi,Jean Costa and Julien Paolini Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 7¦Á-hydroxy-spongia-9(11),13-dien-16-one C20H28O3 ÏàËÆ¶È:60% Tetrahedron 2003 59 9523-9536 Synthetic studies on the preparation of oxygenated spongiane diterpenes from carvone Antonio Abad, Consuelo Agull¨®, Ana C Cuñat, Ana Bel¨¦n Garcı́a, Carlos Gim¨¦nez-Saiz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . cembrene-C ÏàËÆ¶È:60% Tetrahedron 1983 39 1643-1648 Several new cembranoid diterpenes from three soft corals of the red sea Original Research Article Zvia Kinamoni, Amiram Groweiss, Shmuel Carmely, Yoel Kashman, Yossi Loya Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . Cembrene-C ÏàËÆ¶È:60% The Journal of Organic Chemistry 1981 46 3592-3596 Further cembranoid derivatives from the Red Sea soft corals Alcyonium flaccidum and Lobophytum crassum Yoel Kashman, Shmuel Carmely, Amiram Groweiss Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-20 16:01:06













»Ø¸´´ËÂ¥