REACTION OF ALKYL-HALIDES AND ALKYL METHYL ETHERS WITH NITRONIUM TETRAFLUOROBORATE IN ACETONITRILE

被引：23

作者：

BACH, RD

HOLUBKA, JW

TAAFFEE, TA

机构：

[1] Department of Chemistry, Wayne State University, Detroit

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1979年 / 44卷 / 10期

关键词：

D O I：

10.1021/jo01324a044

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of alkyl halides and alkyl ethers with nitronium tetrafluoroborate in acetonitrile affords acetamides by electrophilic cleavage of the carbon-heteroatom bond and trapping the resulting trivalent carbenium ion with acetonitrile. © 1979, American Chemical Society. All rights reserved.

引用

页码：1739 / 1740

页数：2

共 10 条

[1] REACTION OF OPTICALLY-ACTIVE EXO-2-BROMONORBORNANE AND ENDO-2-BROMONORBORNANE WITH NITRONIUM TETRAFLUOROBORATE IN ACETONITRILE - EVIDENCE FOR A CARBENIUM ION PATHWAY [J].