VERSATILE RELATIVE AND ABSOLUTE STEREOCONTROL IN STANNOUS TRIFLATE MEDIATED ALDOL-TYPE REACTIONS OF 3-(2-BENZYLOXYACETYL)THIAZOLIDINE-2-THIONE

被引：88

作者：

MUKAIYAMA, T

IWASAWA, N

机构：

来源：

CHEMISTRY LETTERS | 1984年 / 05期

关键词：

D O I：

10.1246/cl.1984.753

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：753 / 756

页数：4

共 12 条

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[2]

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[4] ACYCLIC STEREOSELECTION .14. O-ALKYLLACTIC ACID-ESTERS - REAGENTS FOR THE STEREOSELECTIVE CONSTRUCTION OF ERYTHRO-ALPHA-METHYL-ALPHA,BETA-DIHYDROXY AND THREO-ALPHA-METHYL-ALPHA,BETA-DIHYDROXY CARBONYL-COMPOUNDS [J].

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[5]

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[6]

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[7] ENANTIOSELECTIVE CROSS ALDOL REACTION VIA DIVALENT TIN ENOLATE [J].

IWASAWA, N ;

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CHEMISTRY LETTERS, 1982, (09) :1441-1444

[8] HIGHLY ENANTIOSELECTIVE ALDOL-TYPE REACTION OF 3-ACETYLTHIAZOLIDINE-2-THIONE WITH ACHIRAL ALDEHYDES [J].

IWASAWA, N ;

MUKAIYAMA, T .

CHEMISTRY LETTERS, 1983, (03) :297-298

[9] STANNOUS TRIFLATE MEDIATED ALDOL REACTION OF 3-ACYLTHIAZOLIDINE-2-THIONE - A CONVENIENT METHOD FOR THE STEREOSELECTIVE SYNTHESES OF BETA-HYDROXY ALDEHYDE AND BETA-HYDROXY CARBOXYLIC-ACID DERIVATIVES [J].

MUKAIYAMA, T ;

IWASAWA, N .

CHEMISTRY LETTERS, 1982, (12) :1903-1906

[10]

MUKAIYAMA T, 1982, ORG REACTIONS, V28, pCH3

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