Sulfoximine-directed ruthenium-catalyzed ortho -C-H Alkenylation of (Hetero)Arenes: Synthesis of EP3 receptor antagonist analogue

dc.contributor.author Yadav, M. Ramu
dc.contributor.author Rit, Raja K.
dc.contributor.author Shankar, Majji
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T08:33:57Z
dc.date.available 2022-03-27T08:33:57Z
dc.date.issued 2014-07-03
dc.description.abstract The reusable sulfoximine directing-group-assisted Ru(II)-catalyzed chemo- and regioselective ortho-C-H alkenylation of arenes and heteroarenes with acrylates and α,β-unsaturated ketones/vinyl sulfone is shown. The N-aroyl sulfoximine undergoes annulation with diphenylacetylene, delivering isoquinolinones and methyl phenyl sulfoxide. The present protocol is successfully employed for the synthesis of the EP3 receptor antagonist analogue. © 2014 American Chemical Society.
dc.identifier.citation Journal of Organic Chemistry. v.79(13)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo5008465
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jo5008465
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/10838
dc.title Sulfoximine-directed ruthenium-catalyzed ortho -C-H Alkenylation of (Hetero)Arenes: Synthesis of EP3 receptor antagonist analogue
dc.type Journal. Article
dspace.entity.type
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