DIASTEREOSELECTIVE [4+2] CYCLOADDITIONS OF ACYL NITROSO-COMPOUNDS

被引：75

作者：

MARTIN, SF

HARTMANN, M

JOSEY, JA

机构：

[1] Department of Chemistry and Biochemistry, The University of Texas, Austin

来源：

TETRAHEDRON LETTERS | 1992年 / 33卷 / 25期

关键词：

D O I：

10.1016/S0040-4039(00)92508-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A highly diastereoselective route to unsaturated amino alcohol derivatives has been developed that features the [4+2] cycloaddition of chiral acyl nitroso compounds to a variety of conjugated dienes; a useful oxidative method for generating acyl nitroso compounds from the corresponding hydroxamic acids under very mild conditions was also discovered.

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页码：3583 / 3586

页数：4

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