COMPETITIVE PATHWAYS IN THE REACTION BETWEEN AROMATIC AZOSULFIDES AND ENOLATES IN DMSO

被引：5

作者：

DELLERBA, C ^{[1
]}

NOVI, M ^{[1
]}

PETRILLO, G ^{[1
]}

TAVANI, C ^{[1
]}

机构：

[1] UNIV GENOA,CNR,CTR STUDIO DIARILOIDI & LORO APPLICAZ,I-16132 GENOA,ITALY

来源：

PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS | 1993年 / 74卷 / 1-4期

关键词：

D O I：

10.1080/10426509308038139

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The outcome of the reaction between azosulfides 1 and ketone enolates is influenced by the presence of suitable alkyl substituents on the aryl moiety of 1. The system can thus be conveniently exploited for the selective synthesis of different classes of derivatives of remarkable applicative interest, namely alpha-aryl ketones, alpha-arylhydrazono ketones, or indazoles.

引用

页码：409 / 410

页数：2

共 7 条

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