Silver-mediated oxidative annulation of: N -arylthio succinimides with alkynes: Direct access to benzo [b] thiophenes

dc.contributor.author Ramesh, E.
dc.contributor.author Shankar, Majji
dc.contributor.author Dana, Suman
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T09:58:14Z
dc.date.available 2022-03-27T09:58:14Z
dc.date.issued 2016-09-01
dc.description.abstract A convenient synthetic route to 2,3-diarylbenzo[b]thiophene derivatives via Ag-catalyzed intermolecular oxidative cyclization between bench-stable N-arylthio succinimides and unactivated internal alkynes is demonstrated herein. The reaction indicates a broad scope, facilitating the construction of diverse arrays of π-conjugated 2,3-diaryl substituted benzothiophenes. The method involves oxidative cleavage of the S-N bond and annulation of alkynes with the concurrent 1,2-S-migration to yield benzo[b]thiophenes.
dc.identifier.citation Organic Chemistry Frontiers. v.3(9)
dc.identifier.issn 20524110
dc.identifier.uri 10.1039/c6qo00259e
dc.identifier.uri http://xlink.rsc.org/?DOI=C6QO00259E
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13485
dc.title Silver-mediated oxidative annulation of: N -arylthio succinimides with alkynes: Direct access to benzo [b] thiophenes
dc.type Journal. Article
dspace.entity.type
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