Enantiospecific Syntheses of Sphingosine and Ceramide Stereoisomers with 3S Configuration from D-Glucose(Organic Chemistry)
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概要
- 論文の詳細を見る
Utilizing the carbon framework (C3-C6) and chirality (at C4 and C5) of D-glucose, (2S, 3S, 4E and 2R, 3S, 4E)-2-amino-4-octadeceiie-1, 3-diol (sphingosine analogues) and four Stereoisomers (2S, 3S, 4E-, 2S, 3S, 4Z-, 2R, 3S, 4E-, and 2R, 3S, 4Z-) of the ceramide derivatives were synthesized in a stereocontrolled way.
- 社団法人日本農芸化学会の論文
- 1991-10-23
著者
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Fujita Shuji
Mect Corporation
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OGAWA Tomoya
RIKEN(Institute of the Physical and chemical Research)
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Ogawa Tomoya
Riken (the Institute Of Physical And Chemical Research)
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Ogawa Tomoya
Riken(the Institute Of Physical And Chemical Research)
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NAKAHARA Yoshiaki
RIKEN (The Institute of Physical and Chemical Research)
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Nakahara Yoshiaki
Riken(the Institute Of Physical And Chemical Research)
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Tomita Kenkichi
Mect Corporation
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SUGIMOTO Mamoru
MECT Corporation
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