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.
引用
收藏
页码：1 / 9
页数：9
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