Synthesis of heteroaryl ketones via tandem reaction of 1,1-dibromoethenes
摘要:
A novel method for the synthesis of heteroaryl ketones through one-pot tandem reaction of 1,1-dibromoethenes with 2-amino(thio)phenols promoted by TBAF center dot 3H(2)O and RuCl3(5%)/air was developed. This novel method includes several reactions in one-pot and utilizes economical yet efficient reagents to generate synthetically and biologically interesting heteroaryl ketones under mild conditions with good efficiency. (C) 2011 Elsevier Ltd. All rights reserved.
RuCl3·3H2O Catalyzed Tandem Reaction of Alkynylbromides with 2-Aminothiophenols in Water: A Convenient Synthesis of 2-Benzoylbenzothiazoles
作者:Xuesen Fan、Yan He、Shenghai Guo、Xinying Zhang
DOI:10.1071/ch11217
日期:——
RuCl3·3H2Ocatalyzedtandemreaction of alkynyl bromides with 2-aminothiophenols mediated by water is shown to represent a convenient synthesis of 2-benzoylbenzothiazoles. In addition, the Ru(iii) catalyst could be readily recovered and efficiently reused together with water up to three times.
A Sustainable Synthesis of 2-Benzoxazyl and 2-Benzothiazyl Ketones from Alkynyl Bromides and 2-Amino(thio)phenols Promoted by a Recyclable Catalytic System
作者:Liangyan Cui、Yan He、Xuesen Fan
DOI:10.1002/cjoc.201100472
日期:2012.4
An environmentally and economically sustainablesynthesis of 2‐benzoxazyl ketones and 2‐benzothiazyl ketones through FeCl3·6H2O catalyzed tandem reactions of alkynylbromides with 2‐amino(thio)phenols in [bmim]BF4 has been developed. Remarkable advantages of this new synthetic strategy include high efficiency, readily available starting materials, and recyclable catalyst and reaction medium.
Elemental sulfur mediated 2-substituted benzothiazole formation from 2-aminobenzenethiols and arylacetylenes or styrenes under metal-free conditions
作者:Guozheng Li、Jingjing Jiang、Feng Zhang、Fuhong Xiao、Guo-Jun Deng
DOI:10.1039/c7ob02430d
日期:——
An oxidative cyclization of 2-aminothiophenols and arylacetylenes or styrenes for the synthesis of 2-alkylbenzothiazoles and 2-acylbenzothiazoles has been developed. Elemental sulfur was used as the effective oxidant to give the corresponding product in good yield under metal-free conditions.
Manganese triacetate is introduced as a new reagent to replace potassiumferricyanide or bromine for radical cyclization of substituted thioformanilides. 2-Substituted benzothiazoles are generated in 6 min under microwave irradiation.