Efficient stereocontrolled synthesis of D-erythro-sphingosine from N-benzoyl-D-glucosamine

被引:28
|
作者
Murakami, T
Hato, M
机构
[1] National Institute of Materials and Chemical Research, Tsukuba, Ibaraki 305
来源
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1996年 / 08期
关键词
D O I
10.1039/p19960000823
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
D-erythro-Sphingosine is synthesized from N-benzoyl-D-glucosamine 2 in a highly regio- and stereo-controlled manner; The key features in the synthesis involve the efficient conversion of compound 2 into the vinyl epoxide 10 and the subsequent S(N)2'-type reaction with a Grignard reagent in the presence of CuCN to afford the 1-O,2-N-protected sphingosine 11.
引用
收藏
页码:823 / 827
页数:5
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