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A Facile Synthesis of 3-(Arylthio)imidazo[1,2-a]pyridin-2(3H)-ones from 2-Aminopyridinium Bromides and Sodium Arenesulfinates

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dc.contributor.author Kumar, Anil
dc.date.accessioned 2021-10-14T13:10:00Z
dc.date.available 2021-10-14T13:10:00Z
dc.date.issued 2020-08-11
dc.identifier.uri https://onlinelibrary.wiley.com/doi/abs/10.1002/adsc.202000633
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2813
dc.description.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. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Chemistry en_US
dc.subject Imidazoheterocycles en_US
dc.subject Radical C−H Bond en_US
dc.title A Facile Synthesis of 3-(Arylthio)imidazo[1,2-a]pyridin-2(3H)-ones from 2-Aminopyridinium Bromides and Sodium Arenesulfinates en_US
dc.type Article en_US


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