ENANTIOFACE DIFFERENTIATING MICHAEL REACTION OF ETHYL ACETOACETATE WITH ALKYLIDENEMALONATES VIA CHIRAL ENAMINE

被引：22

作者：

TOMIOKA, 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 / 38期

关键词：

D O I：

10.1016/S0040-4039(00)85018-2

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：4611 / 4614

页数：4

共 20 条

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[13]

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[15]

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[16]

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[18]

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[19] A DIASTEREOSELECTIVE AND ENANTIOSELECTIVE MICHAEL ADDITION OF CHIRAL AMIDE ENOLATES TO PI,BETA-UNSATURATED ESTERS - A STEREOSELECTIVE SYNTHESIS OF (+)-DEHYDROIRIDODIOL AND (-)-ISODEHYDROIRIDODIOL [J].

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TETRAHEDRON LETTERS, 1986, 27 (08) :959-962

[20] ASYMMETRIC CONJUGATE ADDITION OF COPPER AZAENOLATES AS SYNTHETIC EQUIVALENT OF ENOLATES TO CYCLIC ENONES [J].

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TETRAHEDRON LETTERS, 1982, 23 (36) :3711-3714

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