Electricity mediated [3+2]-cycloaddition of N-sulfonylcyclopropanes with olefins via N-centered radical intermediates: access to cyclopentane analogs

dc.contributor.author	Saha, D.
dc.contributor.author	Taily, I.M.
dc.contributor.author	Banerjee, N.
dc.contributor.author	Banerjee, P.
dc.date.accessioned	2022-05-31T19:42:22Z
dc.date.available	2022-05-31T19:42:22Z
dc.date.issued	2022-06-01
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/3468
dc.description.abstract	An external oxidant free electrochemical strategy is designed towards the β-scission of strained C-C bonds in cyclopropylamine. Moreover, the mechanistic studies ascertained that the methodology encompasses the N-center radical (NCRs) route and provides access to di- or tri-substituted cyclopentane analogs.	en_US
dc.language.iso	en_US	en_US
dc.title	Electricity mediated [3+2]-cycloaddition of N-sulfonylcyclopropanes with olefins via N-centered radical intermediates: access to cyclopentane analogs	en_US
dc.type	Article	en_US