Cyclisation of aryl acetylides with isothiocyanates: new insight into an old reaction

被引：4
|
作者：
Adams, Harry [1 ]
Hodson, Hannah [1 ]
Morris, Michael J. [1 ]
Venting, Gareth A. [1 ]
机构：
[1] Univ Sheffield, Dept Chem, Sheffield S3 7HF, S Yorkshire, England
来源：
TETRAHEDRON LETTERS | 2016年 / 57卷 / 12期
关键词：
Alkyne; 3-Imino-1,2-dithiole; Isothiocyanate; Heterocycle; Thioamide;
D O I：
10.1016/j.tetlet.2016.02.034
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The reaction of lithium phenylacetylide with phenyl isothiocyanate followed by the addition of ethanol produces a crystallographically-characterised heterocycle formed by the cyclisation of two molecules each of acetylene and isothiocyanate, and which is identical to the dimer of the acetylenic thioamide PhC CC(=S)NHPh, described almost a century ago. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码：1328 / 1330
页数：3
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