HIGHLY ENANTIOSELECTIVE ALDOL-TYPE REACTION OF 3-ACETYLTHIAZOLIDINE-2-THIONE WITH ACHIRAL ALDEHYDES

被引：74

作者：

IWASAWA, N

MUKAIYAMA, T

机构：

来源：

CHEMISTRY LETTERS | 1983年 / 03期

关键词：

D O I：

10.1246/cl.1983.297

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

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页码：297 / 298

页数：2

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共 7 条

[1] ASYMMETRIC-SYNTHESIS OF BETA-HYDROXY ESTERS BY REFORMATSKY REACTIONS AND AMIDE BASE MEDIATED CONDENSATIONS
BRANDANGE, S
JOSEPHSON, S
MORCH, L
VALLEN, S
[J]. ACTA CHEMICA SCANDINAVICA SERIES B-ORGANIC CHEMISTRY AND BIOCHEMISTRY, 1981, 35 (04): : 273 - 277
[2] ELIEL EL, 1982, ASYMMETRIC REACTIONS, P70
[3] ASYMMETRICAL SYNTHESIS OF BETA-HYDROXY ESTERS BY REFORMATSKY REACTION IN PRESENCE OF (-) SPARTEINE
GUETTE, M
CAPILLON, J
GUETTE, JP
[J]. TETRAHEDRON, 1973, 29 (22) : 3659 - 3667
[4] GUETTE M, 1971, TETRAHEDRON LETT, P2863
[5] ACYCLIC STEREOSELECTION .11. DOUBLE STEREO-DIFFERENTIATION AS A METHOD FOR ACHIEVING SUPERIOR CRAMS RULE SELECTIVITY IN ALDOL CONDENSATIONS WITH CHIRAL ALDEHYDES
HEATHCOCK, CH
WHITE, CT
MORRISON, JJ
VANDERVEER, D
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1981, 46 (07) : 1296 - 1309
[6] ENANTIOSELECTIVE CROSS ALDOL REACTION VIA DIVALENT TIN ENOLATE
IWASAWA, N
MUKAIYAMA, T
[J]. CHEMISTRY LETTERS, 1982, (09) : 1441 - 1444
[7] 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
MUKAIYAMA, T
IWASAWA, N
[J]. CHEMISTRY LETTERS, 1982, (12) : 1903 - 1906