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

Ramesh, E. ; Shankar, Majji ; Dana, Suman ; Sahoo, Akhila K. (2016) Silver-mediated oxidative annulation of N-arylthio succinimides with alkynes: direct access to benzo[b]thiophenes Organic Chemistry Frontiers, 3 (9). pp. 1126-1130. ISSN 2052-4129

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Official URL: http://doi.org/10.1039/C6QO00259E

Related URL: http://dx.doi.org/10.1039/C6QO00259E

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.

Item Type:Article
Source:Copyright of this article belongs to Royal Society of Chemistry.
ID Code:121877
Deposited On:22 Jul 2021 19:18
Last Modified:22 Jul 2021 19:18

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