NOVEL REACTIONS OF 3-UNSUBSTITUTED 3-ISOXAZOLIN-5-ONES

被引：20

作者：

WOODMAN, DJ

BORMAN, CH

TONTAPAN.N

STONEBRA.PM

机构：

[1] Department of Chemistry, University of Washington, Seattle

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1969年 / 34卷 / 10期

关键词：

D O I：

10.1021/jo01262a039

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of 2,4-diphenyl-3-isoxazolin-5-one, 4, and ethoxide gives ethyl2-phenylmalonanilate, 7, while that of2-methyl-4-carbethoxy-3-isoxazolin-5-one, 2, with acetate gives an enolic C-acyl derivative, 23 (R = Me). Both reactions may involve rearrangement of the normal ring-opening products. © 1969, American Chemical Society. All rights reserved.

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页码：2981 / &

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