ASYMMETRIC MICHAEL ADDITIONS - REGIO-SELECTIVE, DIASTEREO-SELECTIVE, AND ENANTIOSELECTIVE ALKYLATIONS OF THE ENAMINES FROM BETA-TETRALONES AND (S)-2-(METHOXYMETHYL)PYRROLIDINE (PROLINOL METHYL-ETHER) BY OMEGA-NITROSTYRENES

被引：68

作者：

BLARER, SJ ^{[1
]}

SEEBACH, D ^{[1
]}

机构：

[1] SWISS FED INST TECHNOL,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND

来源：

CHEMISCHE BERICHTE-RECUEIL | 1983年 / 116卷 / 09期

关键词：

D O I：

10.1002/cber.19831160908

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：3086 / 3096

页数：11

共 18 条

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[2] ASYMMETRIC MICHAEL ADDITIONS - STEREOSELECTIVE ALKYLATIONS OF THE (R)-ENAMINE AND (S)-ENAMINE FROM CYCLOHEXANONE AND 2-(METHOXYMETHYL)PYRROLIDINE BY METHYL ALPHA-(METHOXYCARBONYL)CINNAMATES [J].

BLARER, SJ ;

SEEBACH, D .

CHEMISCHE BERICHTE-RECUEIL, 1983, 116 (06) :2250-2260

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[8] TAUTOMERISM OF ENAMINES DERIVED FROM 2-TETRALONE - DIFFERENCE IN NUCLEOPHILIC BEHAVIOR BETWEEN MORPHOLINE AND PYRROLIDINE ENAMINES [J].

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