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段媛昌

铁虫 (小有名气)

[求助] 求助mdc-9 已有1人参与

63.0,64.4,68.2,72.5,106.2,109.7,114.7,129.5,141.8
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yangyinhe

至尊木虫 (著名写手)

【答案】应助回帖

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感谢参与,应助指数 +1
段媛昌(卓越_先锋代发): 金币+7, 有人应助后,请及时发放金币 版规详见http://emuch.net/bbs/viewthread.php?tid=6767355&pid=1#pid1 2015-04-02 15:02:46
1 .     established 2S-configuration
    相似度:55.5%
Chemical & Pharmaceutical Bulletin          1991          39          2277-2281
Studies on Glycolipids. III. Glyceroglycolipids from an Axenically Cultured Cyanobacterium, Phormidium tenue
Nobutoshi MURAKAMI,Takashi MORIMOTO,Hideaki IMAMURA,Taisei UEDA,Shin-ichi NAGAI,Jinsaku SAKAKIBARA and Naoki YAMADA
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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2 .     (2'S)-2'-O-(tetradecanoyl)-3'-O-(9Z,12Z,15Z-octadecatrienoyl0-glyceryl-β-D-galactopyranoside
    相似度:55.5%
Chemical & Pharmaceutical Bulletin          1990          38          3497-3499
SEVEN NEW MONOGALACTOSYL DIACYLGLYCEROLS ISOLATED FROM THE AXENIC CYANOBACTERIUM PHORMIDIUM TENUE
Nobutoshi MURAKAMI,Hideaki IMAMURA,Jinsaku SAKAKIBARA and Naoki YAMADA
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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3 .     (2S)-1-O-(7Z,10Z,13 Z)-hexadecatrienoyl-2-O-(7Z,10Z)-hexadecadienoyl-3-O-β-D-galactopyranosyl-sn-glycerol
    相似度:55.5%
Phytochemistry          1995          40          1433-1437
Anti-tumour-promoting glyceroglycolipids from the green alga, Chlorella vulgaris
Takashi Morimoto, Akito Nagatsu, Nobutoshi Murakami, Jinsaku Sakakibara, Harukuni Tokuda, Hoyoku Nishino, Akio Iwashima
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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4 .     (2S)-1,2-di-O-(7Z,10Z)-hexadecadienoyl-3-O-β-D-galactopyranosyl-sn-glycerol
    相似度:55.5%
Phytochemistry          1995          40          1433-1437
Anti-tumour-promoting glyceroglycolipids from the green alga, Chlorella vulgaris
Takashi Morimoto, Akito Nagatsu, Nobutoshi Murakami, Jinsaku Sakakibara, Harukuni Tokuda, Hoyoku Nishino, Akio Iwashima
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

--------------------------------------------------------------------------------

5 .     comopund 1
    相似度:55.5%
Tetrahedron Letters          2000          41          7875-7878
Solid phase Diels–Alder/retro Diels–Alder reactions. A new method for traceless linker strategy
Luis Blanco, Robert Bloch, Emmanuelle Bugnet, Sandrine Deloisy
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

--------------------------------------------------------------------------------

6 .     compound
    相似度:55.5%
European Journal of Organic Chemistry          2011                   6039-6055
Towards the Synthesis of the 4,19-Diol Derivative of (–)-Mycothiazole: Synthesis of a Potential Key Intermediate
Frédéric Batt and Fabienne Fache
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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7 .     1,2-O-isopropylidene-β-D-psicopyranose
    相似度:55.5%
European Journal of Organic Chemistry          2011                   2286-2292
Controlled Garegg Conditions for Selective Iodination on Pyranose Templates
Ana-Catarina Simao, Sandrina Silva, Amelia P. Rauter, Patrick Rollin and Arnaud Tatibouët
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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8 .     (1S,3R)-1-(Furan-2-yl)hept-6-ene-1,3-diol
C11H16O3     相似度:54.5%
Tetrahedron          2014          70          2096-2101
Enantioselective synthesis of macrolactone core of the natural product Sch725674
Sunil Kumar Sunnam, Kavirayani R. Prasad
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

--------------------------------------------------------------------------------

9 .     1-deoxy-l-erythritol 3-O-β-D-glucopyranoside
C10H20O8     相似度:50%
Phytochemistry          2003                   609-616
Aromatic compound glucosides, alkyl glucoside and glucide from the fruit of anise
Eiko Fujimatu, Toru Ishikawa, Junichi Kitajima
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

--------------------------------------------------------------------------------

10 .     4-[(Z)-(4-hydroxy-3-methyl-2-butenyl)oxy]benzaldehyde
C12H14O3     相似度:50%
Journal of Natural Products          1993          Vol 56          85
Metabolites of Peniophora polygonia, Part 2. Some Aromatic Compounds
William A. Ayer, Latchezar S. Trifonov
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