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

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DC Field	Value	Language
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
Appears in Collections:	Year-2022

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