| ²é¿´: 444 | »Ø¸´: 1 | |||
Æë¾ý½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
22.0,39.3,43.2,68.5,69.5,70.7,114.7,118.7,122.5,128.9,133.3,145.8,149.7,163.8,205.4 ÈܼÁÊÇMeOD [ Last edited by ׿Խ_ÏÈ·æ on 2015-6-8 at 15:57 ] |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸085404£¬×Ü·Ö291£¬Ëļ¶Òѹý£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁÏר˶µ÷¼Á
ÒѾÓÐ9È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ21È˻ظ´
»úеµ÷¼Á
ÒѾÓÐ3È˻ظ´
368»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0703µ÷¼Á£¬Ò»Ö¾Ô¸Ìì½ò´óѧ319·Ö
ÒѾÓÐ21È˻ظ´
0854µç×ÓÐÅÏ¢319Çóµ÷¼Á£¨½ÓÊÜ¿çרҵµ÷¼Á£©
ÒѾÓÐ6È˻ظ´
µ÷¼Á
ÒѾÓÐ15È˻ظ´
yangyinhe
ÖÁ×ðľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1566 (½²Ê¦)
- ½ð±Ò: 15048.4
- ºì»¨: 21
- Ìû×Ó: 2773
- ÔÚÏß: 261.2Сʱ
- ³æºÅ: 942922
- ×¢²á: 2010-01-15
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Æë¾ý: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-09 10:43:40
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Æë¾ý: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-06-09 10:43:40
|
Coniothyrinone A C15H16O5 ÏàËÆ¶È:66.6% Chirality 2013 25 141-148 Structural and Stereochemical Studies of Hydroxyanthraquinone Derivatives from the Endophytic Fungus Coniothyrium sp Peng Sun, Juan Huo, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Hua Tang, Siegfried Draeger, Barbara Schulz, Hidayat Hussain, Karsten Krohn, Weihua Pan, Yanghua Yi and Wen Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Coniothyrinone A C15H16O5 ÏàËÆ¶È:66.6% Chirality 2013 25 141-148 Structural and Stereochemical Studies of Hydroxyanthraquinone Derivatives from the Endophytic Fungus Coniothyrium sp (pages 141¨C148) Peng Sun, Juan Huo, Tibor Kurt¨¢n, Attila M¨¢ndi, S¨¢ndor Antus, Hua Tang, Siegfried Draeger, Barbara Schulz, Hidayat Hussain, Karsten Krohn, Weihua Pan, Yanghua Yi and Wen Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (R)-6-[(S)-2-hydroxy-4-(4-hydroxyphenyl)butyl]-5,6-dihydropyran-2-one C15H18O4 ÏàËÆ¶È:60% Journal of Natural Products 2007 70 2006-2009 Structure Elucidation of a Dihydropyranone from Tapinanthus dodoneifolius Maurice Ouedraogo,H¨¦l¨¨ne Carreyre, Clarisse Vandebrouck,Jocelyn Bescond, Guy Raymond,Innocent-Pierre Guissou, Christian Cognard, Fr¨¦d¨¦ric Becq, Daniel Potreau, Alain Cousson, J¨¦rôme Marrot,O and Jean-Marie Coustard Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound C19H22O7S ÏàËÆ¶È:60% The Journal of Antibiotics 2011 64 781-787 Total synthesis and absolute configuration of avenolide, extracellular factor in Streptomyces avermitilis Miho Uchida, Satoshi Takamatsu, Shiho Arima, Kiyoko T Miyamoto, Shigeru Kitani, Takuya Nihira, Haruo Ikeda and Tohru Nagamitsu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (3R*,4R*)-3-(5-bromofuran-2-yl)-2-methyl-N-(4-methylbenzyl)-1,2-oxazolidine-4-sulfonamide C16H19BrN2O4S ÏàËÆ¶È:60% Chemical Biology & Drug Design 2010 75 461-474 Inhibition of HIV-1 Replication by Isoxazolidine and Isoxazole Sulfonamides Belinda Loh, Luciano Vozzolo, B. James Mok, Chien Chi Lee, Richard J. Fitzmaurice, Stephen Caddick and Ariberto Fassati Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-06-09 08:41:55














»Ø¸´´ËÂ¥