ASYMMETRIC-SYNTHESIS OF THREO-SPHINGOSINES AND ERYTHRO-SPHINGOSINES BY ASYMMETRIC ALDOL REACTION OF ALPHA-ISOCYANOACETATE CATALYZED BY A CHIRAL FERROCENYLPHOSPHINE-GOLD(I) COMPLEX

被引：99

作者：

ITO, Y

SAWAMURA, M

HAYASHI, T

机构：

来源：

TETRAHEDRON LETTERS | 1988年 / 29卷 / 02期

关键词：

D O I：

10.1016/S0040-4039(00)80064-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

收藏

页码：239 / 240

页数：2

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[1] ALPHA-AMINO-ACID DERIVATIVES AS CHIRAL EDUCTS FOR ASYMMETRIC PRODUCTS - SYNTHESIS OF SPHINGOSINE FROM ALPHA'-AMINO-ALPHA,BETA-YNONES
BOUTIN, RH
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[2] CATALYTIC ASYMMETRIC ALDOL REACTION - REACTION OF ALDEHYDES WITH ISOCYANOACETATE CATALYZED BY A CHIRAL FERROCENYLPHOSPHINE-GOLD(I) COMPLEX
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[3] ITO Y, IN PRESS TETRAHEDRON
[4] ENANTIOSELECTIVE SYNTHESIS OF D-ERYTHRO-SPHINGOSINE AND OF CERAMIDE
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[5] SYNTHESIS OF D-ERYTHRO-SPHINGOSINES
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[6] USEFUL SYNTHESES OF ERYTHRO-N-OLEOYL-D-SPHINGOSINE AND THREO-N-OLEOYL-D-SPHINGOSINE (CERAMIDES) AND GALACTOSYLCERAMIDES (CEREBROSIDES) FROM L-SERINE
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