EFFICIENT SYNTHESIS OF NEW STABLE 1,4-DIIONIC ORGANOSULFURS AND CORRESPONDING MESOIONIC COMPOUNDS FROM N-HETEROCYCLIC YLIDES

被引：3

作者：

Shahrekipour, Fahimeh ^{[1
]}

Heydari, Reza ^{[1
]}

Tahamipour, Batool ^{[2
]}

Saravani, Hamideh ^{[1
]}

Graiff, Claudia ^{[3
]}

机构：

[1] Univ Sistan & Baluchestan, Fac Sci, Dept Chem, Zahedan 98135674, Iran

[2] Farhangian Univ Kerman, Kerman, Iran

[3] Univ Parma, Dipartimento Chim, I-43100 Parma, Italy

来源：

PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS | 2014年 / 189卷 / 02期

关键词：

2-Bromoacetophenone; mesoionic compounds; benzoyl isothiocyanate; 1,3-dipolar cycloaddition; nitrogen ylides; AZOLOPYRIDINE SERIES; CHEMISTRY; SYSTEMS; ISOTHIOCYANATES; DERIVATIVES;

D O I：

10.1080/10426507.2013.819866

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

N-Phenacyl heterocyclic salts such as isoquinolinium, quinolinium, and pyridinium bromide react quickly with benzoyl isothiocyanate in the present of triethylamine to produce 1,4-diionic organosulfur derivatives. Cyclization and dehydrogenation of 1,4-diionic organosulfurs gave thiazoloisoquinolinium, quinolinium, or pyridinium benzimidates. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements for the following free supplemental files: Figures.].

引用

页码：263 / 273

页数：11

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