Electrochemical access to benzimidazolone and quinazolinone derivatives via in situ generation of isocyanates

dc.contributor.author	Saha, D.
dc.contributor.author	Taily, I. M.
dc.contributor.author	Naik, S.
dc.contributor.author	Banerjee, P.
dc.date.accessioned	2021-07-25T11:53:19Z
dc.date.available	2021-07-25T11:53:19Z
dc.date.issued	2021-07-25
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/2231
dc.description.abstract	Isocyanates are the key intermediates for several organic transformations towards the synthesis of diverse pharmaceutical targets. Herein, we report the development of an oxidant-free protocol for electrochemical in situ generation of isocyanates. This strategy highlights expedient access to benzimidazolones and quinazolinones and eliminates the need for exogenous oxidants. Furthermore, detailed mechanistic studies provide strong support towards our hypothesis of in situ isocyanate generation.	en_US
dc.language.iso	en_US	en_US
dc.title	Electrochemical access to benzimidazolone and quinazolinone derivatives via in situ generation of isocyanates	en_US
dc.type	Article	en_US