THE CONTROL OF DIASTEREOSELECTIVITY IN THE MICHAEL REACTION OF KETONIC ENOLATES WITH CROTONIC ACID-DERIVATIVES

被引：13

作者：

COREY, EJ

HOUPIS, IN

机构：

[1] Department of Chemistry, Harvard University, Cambridge

来源：

TETRAHEDRON LETTERS | 1993年 / 34卷 / 15期

关键词：

D O I：

10.1016/S0040-4039(00)60431-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Methodology is described for the selective generation of either anti or syn Mi

引用

页码：2421 / 2424

页数：4

共 15 条

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[3] ENANTIOSELECTIVE MICHAEL REACTIONS - STEREOSELECTIVE ADDITION OF ENOLATES OF PHENMENTHOL ESTERS TO CROTONATES
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[6] MULZER J, 1983, J CHEM SOC CHEM COM
[7] ACYCLIC STEREOSELECTION .47. STEREOCHEMISTRY OF THE MICHAEL ADDITION OF ESTER AND KETONE ENOLATES TO ALPHA,BETA-UNSATURATED KETONES
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (01) : 157 - 172
[8] ACYCLIC STEREOSELECTION .46. STEREOCHEMISTRY OF THE MICHAEL ADDITION OF N,N-DISUBSTITUTED AMIDE AND THIOAMIDE ENOLATES TO ALPHA,BETA-UNSATURATED KETONES
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[J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (01) : 132 - 157
[9] OARE DA, 1991, TOP STEREOCHEM, V20, P87
[10] OARE DA, 1989, TOP STEREOCHEM, V19, P227

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