DIASTEREOSELECTIVE AZOMETHINE YLIDE CYCLOADDITIONS TO UNSATURATED, CHIRAL BICYCLIC LACTAMS

被引：29

作者：

FRAY, AH ^{[1
]}

MEYERS, AI ^{[1
]}

机构：

[1] COLORADO STATE UNIV,DEPT CHEM,FT COLLINS,CO 80523

来源：

TETRAHEDRON LETTERS | 1992年 / 33卷 / 25期

基金：

美国国家卫生研究院;

关键词：

D O I：

10.1016/S0040-4039(00)92506-1

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The levels of diastereoselection resulting from the 1,3-dipolar cycloaddition of chiral and achiral azomethine ylides 2(a-c) to chiral, unsaturated bicyclic lactams 1(a-f) are described in terms of steric factors.

引用

页码：3575 / 3578

页数：4

共 24 条

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[5] CHIRAL INDUCTION IN CYCLOADDITION REACTIONS OF AZOMETHINE YLIDES DERIVED FROM SECONDARY ALPHA-AMINO-ACIDS BY THE DECARBOXYLATIVE ROUTE
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[J]. TETRAHEDRON LETTERS, 1991, 32 (39) : 5417 - 5420
[6] DIASTEREOFACIAL SELECTIVITY IN THE 1,3-DIPOLAR CYCLOADDITION OF CHIRAL AZOMETHINE YLIDES
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[J]. TETRAHEDRON LETTERS, 1991, 32 (51) : 7531 - 7534
[7] STEREOSELECTIVE 1,3-DIPOLAR CYCLOADDITIONS OF PHOTOCHEMICALLY GENERATED AZOMETHINE YLIDES TO OPPOLZER CHIRAL ACRYLOYL SULTAM - AN ASYMMETRIC APPROACH TO QUINOCARCIN
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HO, WB
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (13) : 3973 - 3975
[8] AN APPROACH TO THE 3,8-DIAZABICYCLO[3.2.1]OCTANE MOIETY OF NAPHTHYRIDINOMYCIN AND QUINOCARCIN VIA 1,3-DIPOLAR CYCLO-ADDITION OF PHOTOCHEMICALLY GENERATED AZOMETHINE YLIDES
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[J]. TETRAHEDRON LETTERS, 1988, 29 (29) : 3525 - 3528
[9] A CORRELATION OF REACTION RATES
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[10] HUISGEN R, 1986, 1 3 DIPOLAR CYCLOADD, V1, P1

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