Formation of reagent-selective products from 2-(4,5-dihydrothiazol-2-ylthio)-1-arylethanone with different nucleophiles

被引：4

作者：

Saravanan, S. ^{[1
]}

Mohan, P. ^{[1
]}

Muthusubramanian, S. ^{[1
]}

机构：

[1] Madurai Kamaraj Univ, Sch Chem, Madurai 625021, Tamil Nadu, India

来源：

JOURNAL OF SULFUR CHEMISTRY | 2011年 / 32卷 / 01期

关键词：

thiazolidinethiol; nucleophiles; selenium dioxide; thionyl chloride; phase transfer catalyst; BIOLOGICAL-ACTIVITY; 1,2,3-THIADIAZOLES; DERIVATIVES; MECHANISM; CHLORIDE;

D O I：

10.1080/17415993.2010.533772

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The reactions of 2-(4,5-dihydrothiazol-2-ylthio)-1-arylethanone with different nucleophiles including semicarbazide hydrochloride, hydroxylamine hydrochloride, hydrazine, ethylenediamine and aminoethanol have been investigated, and the formation of a variety of products with different reagents is highlighted. [GRAPHICS] .

引用

页码：71 / 84

页数：14

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