Pd(II)-catalyzed ortho -C-H oxidation of arylacetic acid derivatives: Synthesis of benzofuranones

dc.contributor.author Rit, Raja K.
dc.contributor.author Yadav, M. Ramu
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T08:34:09Z
dc.date.available 2022-03-27T08:34:09Z
dc.date.issued 2014-02-07
dc.description.abstract Pd(II)-catalyzed ortho-C-H acetoxylation of arylacetic acid derivatives is demonstrated with the aid of a novel S-methyl-S-2-pyridylsulfoximine (MPyS) directing group (DG). The α-mono- and α-unsubstituted arylacetic acid derivatives were readily employed in the ortho-C-H acetoxylations. The oxidation products are hydrolyzed, and the MPyS-DG is easily recovered, providing ready access to o-hydroxyarylacetic acids. 3-Mono- and 3-unsubstituted benzofuranones are synthesized from o-hydroxyarylacetic acids. © 2014 American Chemical Society.
dc.identifier.citation Organic Letters. v.16(3)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/ol403699d
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ol403699d
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/10882
dc.title Pd(II)-catalyzed ortho -C-H oxidation of arylacetic acid derivatives: Synthesis of benzofuranones
dc.type Journal. Article
dspace.entity.type
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