Please use this identifier to cite or link to this item:
http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2813
Title: | A Facile Synthesis of 3-(Arylthio)imidazo[1,2-a]pyridin-2(3H)-ones from 2-Aminopyridinium Bromides and Sodium Arenesulfinates |
Authors: | Kumar, Anil |
Keywords: | Chemistry Imidazoheterocycles Radical C−H Bond |
Issue Date: | 11-Aug-2020 |
Publisher: | Wiley |
Abstract: | Direct C−H bond functionalization through radical pathway has emerged as a powerful and ideal strategy for the synthesis of organic compounds. This review provides an overview of recent developments in radical C−H functionalization of imidazoheterocycles such as imidazo[1,2-a]pyridine, benzo[d]imidazo[2,1-b]thiazole, imidazo[2,1-b]thiazole, imidazo[1,2-a]pyrimidine, imidazo[2,1-a]isoquinoline, imidazo[1,2-a]pyrazine and imidazo[1,2-a]quinoline using organic peroxides, photo/electric-induced protocols, iodine-based reagents, first-row transition metal catalysts (Fe, Mn, Ni and Cu) and inorganic oxidants/or salts. |
URI: | https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.202000633 http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2813 |
Appears in Collections: | Department of Chemistry |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.