STEREOSELECTIVE SYNTHESIS OF CIS-ALPHA,BETA-EPOXYESTERS AND ALDEHYDES VIA DIVALENT TIN ENOLATE - A SYNTHESIS OF 2-AMINO-2-DEOXY-D-ARABINITOL

被引：17

作者：

MUKAIYAMA, T

YURA, T

IWASAWA, N

机构：

来源：

CHEMISTRY LETTERS | 1985年 / 06期

关键词：

D O I：

10.1246/cl.1985.809

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：809 / 812

页数：4

共 6 条

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[2] ACYCLIC STEREOSELECTION .6. REAGENT FOR ACHIEVING HIGH 1,2 DIASTEREOSELECTION IN THE ALDOL CONVERSION OF CHIRAL ALDEHYDES INTO 3-HYDROXY-2-METHYLCARBOXYLIC ACIDS [J].

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[3] STEREOSELECTIVE SYNTHESIS OF CIS-ALPHA, BETA-EPOXYKETONES VIA DIVALENT TIN ENOLATE [J].

MUKAIYAMA, T ;

HAGA, T ;

IWASAWA, N .

CHEMISTRY LETTERS, 1982, (10) :1601-1604

[4] STANNOUS TRIFLATE - A NEW ALDOL REACTION VIA DIVALENT TIN ENOLATES [J].

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STEVENS, RW ;

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CHEMISTRY LETTERS, 1982, (03) :353-356

[5]

Newman M. S., 1951, ORG REACTIONS, V5, P413, DOI 10.1002/0471264180.or005.10

[6] The impact of alkali hydrogen superoxyde on unsaturated compounds. [J].

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