INTRAMOLECULAR NATURE OF REARRANGEMENT OF BENZIMIDATES

被引：16

作者：

WHEELER, OH

ROMAN, F

ROSADO, O

机构：

[1] Department of Chemistry, Puerto Rico Nuclear Center, University of Puerto Rico, Mayaguez, Puerto Rico

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1969年 / 34卷 / 04期

关键词：

D O I：

10.1021/jo01256a041

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Chapman rearrangement of a mixture of 14C-4-bromophenyl N-phenylbenzimidate and 4-bromophenyl N-4-rtolylbenzimidate showed that the reaction was intramolecular. Tritium-labeled allyl N-phenylbenzimidate similarly rearranged exclusively intramolecularly with inversion of the allyl group. © 1969, American Chemical Society. All rights reserved.

引用

页码：966 / &

共 12 条

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