Reactivity of benzylic acylammonium chlorides. A novel method for the synthesis of N-phenacylamides.

被引：8

作者：

Coskun, N

Tirli, F

机构：

[1] Department of Organic Chemistry, Uludaǧ University

来源：

SYNTHETIC COMMUNICATIONS | 1997年 / 27卷 / 01期

关键词：

D O I：

10.1080/00397919708004799

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Tertian amines 1 reacted with acid chlorides 2 to give corresponding benzyl chlorides and N-phenacylamides 4. Counterion in species 3 attacked preferentially the benzylic methylene. Effect of substituents in the benzyl group on the reactivity. of acylammonium chlorides 3 was investigated.

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页码：1 / 9

页数：9

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