ENANTIOSELECTIVE PROTONATION OF ENOLATES - NOVEL CHIRAL PROTON SOURCES AND REMARKABLE EFFECTS OF THE COUNTERCATION

被引：65

作者：

FUJI, K ^{[1
]}

KAWABATA, T ^{[1
]}

KURODA, A ^{[1
]}

TAGA, T ^{[1
]}

机构：

[1] KYOTO UNIV,FAC PHARMACEUT SCI,KYOTO 606,JAPAN

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1995年 / 60卷 / 07期

关键词：

D O I：

10.1021/jo00112a002

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：1914 / 1915

页数：2

共 26 条

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[7] ENANTIOSELECTIVE DEPROTONATION OF 2 RACEMIC CYCLIC CARBONYL-COMPOUNDS BY A CHIRAL LITHIUM AMIDE
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[8] EVANS DA, 1982, TOP STEREOCHEM, V13, P1, DOI DOI 10.1002/9780470147221.CHL
[9] HIGHLY ENANTIOSELECTIVE PROTONATION OF THIOL ESTER ENOLATES
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[J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1993, 32 (07): : 1042 - 1044
[10] SYNTHESIS OF (R)-(+)-ALPHA-DAMASCONE AND (S)-(-)-ALPHA-DAMASCONE BY TANDEM GRIGNARD REACTION-ENANTIOSELECTIVE PROTONATION - EVIDENCE FOR THE INTERMEDIACY OF A CHIRAL COMPLEX
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (20) : 6909 - 6911

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