Diazo Ethers: Formation and Decomposition in the Course of Reactions Between Arenediazonium Ions and Different Alcohols

被引：12

作者：

Bravo-Diaz, Carlos ^{[1
]}

机构：

[1] Univ Vigo, Dept Quim Fis, Fac Quim, Vigo 36310, Spain

来源：

MINI-REVIEWS IN ORGANIC CHEMISTRY | 2009年 / 6卷 / 02期

关键词：

ACIDIC METHANOL; ASCORBIC-ACID; HETEROLYTIC DEDIAZONIATION; BETA-CYCLODEXTRIN; PRODUCT FORMATION; MECHANISM; KINETICS; SALTS; TETRAFLUOROBORATE; REDUCTION;

D O I：

10.2174/157019309788167693

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The present review is aimed to summarize recent research on the O-coupling reactions of arenediazonium, ArN2+, ions with different alcohols under acidic conditions. Encapsulating in a nutshell their mechanisms, it appears that two possible products may be formed depending on experimental conditions, namely a highly unstable aryl cation, Ar+, that yields substitution products and a reactive diazo ether, namely Ar-N=N-O-R, which initiates a radical mechanism through the formation of aryl radicals Ar center dot to yield reduction products.

引用

页码：105 / 113

页数：9

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