Direct access to benzo[b]furans through palladium-catalyzed oxidative annulation of phenols and unactivated internal alkynes

dc.contributor.author	Kuram, Malleswara Rao
dc.contributor.author	Bhanuchandra, M.
dc.contributor.author	Sahoo, Akhila K.
dc.date.accessioned	2022-03-27T08:34:27Z
dc.date.available	2022-03-27T08:34:27Z
dc.date.issued	2013-04-22
dc.description.abstract	2,3-Disubstituted benzo[b]furans are prepared in one step from commercially available phenols and readily accessible unactivated internal alkynes (see scheme). This Pd-catalyzed oxidative annulation has a broad substrate scope and allows access to a wide range of benzo[b]furans. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.identifier.citation	Angewandte Chemie - International Edition. v.52(17)
dc.identifier.issn	14337851
dc.identifier.uri	10.1002/anie.201210217
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/anie.201210217
dc.identifier.uri	https://dspace.uohyd.ac.in/handle/1/10937
dc.subject	alkynes
dc.subject	benzo[b]furans
dc.subject	oxidative annulation
dc.subject	phenols
dc.subject	regioselectivity
dc.title	Direct access to benzo[b]furans through palladium-catalyzed oxidative annulation of phenols and unactivated internal alkynes
dc.type	Journal. Article
dspace.entity.type

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