DIASTEREOSELECTIVITY IN THE INTRAMOLECULAR CYCLOADDITION REACTIONS OF NITRONES DERIVED FROM 5-ALKENALS AND CHIRAL HYDROXYLAMINES

被引：29

作者：

BALDWIN, SW

MCFADYEN, RB

AUBE, J

WILSON, JD

机构：

[1] Department of Chemistry Duke University Durham

来源：

TETRAHEDRON LETTERS | 1991年 / 32卷 / 35期

关键词：

D O I：

10.1016/0040-4039(91)80004-P

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Intramolecular cycloaddition of the nitrones derived from a series of 5-alkenals and alpha-methylbenzyl hydroxylamine leads to mixtures of diastereomeric products in the range of 1.7/1 to 16/1.

引用

页码：4431 / 4434

页数：4

共 16 条

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[9] SYNTHESIS OF SOME N-OXYGENATED PRODUCTS OF 3,4-DIMETHOXY-AMPHETAMINE AND ITS N-ALKYL DERIVATIVES
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[10] PADWA A, 1990, ADV CYCLOADDITION, V2, P1

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