ASYMMETRIC MICHAEL REACTION OF ALPHA-ALKYL BETA-KETO-ESTERS VIA CHIRAL ENAMINES

被引：40

作者：

TOMIOKA, K ^{[1
]}

ANDO, K ^{[1
]}

YASUDA, K ^{[1
]}

KOGA, K ^{[1
]}

机构：

[1] UNIV TOKYO,FAC PHARMACEUT SCI,BUNKYO KU,TOKYO 113,JAPAN

来源：

TETRAHEDRON LETTERS | 1986年 / 27卷 / 06期

关键词：

D O I：

10.1016/S0040-4039(00)84081-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：715 / 716

页数：2

共 12 条

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[5]

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[8] THE ASYMMETRIC MICHAEL REACTION OF (2R,3S)-3,4-DIMETHYL-2-PHENYLPERHYDRO-1,4-OXAZEPINE-5,7-DIONE WITH 1-NITROCYCLOHEXENE [J].

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[9] FACTORS CONTROLLING THE DIASTEREOFACE SELECTIVITY IN THE COMPLEMENTARY ASYMMETRIC ALKYLATION OF ALPHA-ALKYL BETA-KETO-ESTERS [J].

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[10] ASYMMETRIC ALKYLATION OF ALPHA-ALKYL BETA-KETO-ESTERS [J].

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