Pd(II)‐catalyzed, Picolinamide‐aided sp2 γ−C−H Functionalization of Phenylglycinol: Access to γ−C−H Arylated, Alkylated and Halogenated Phenylglycinol Scaffolds

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3427

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DC Field	Value	Language
dc.contributor.author	Singh, Prabhakar	-
dc.contributor.author	Arulananda Babu, S.	-
dc.contributor.author	Aggarwal, Y.	-
dc.contributor.author	Patel, P.	-
dc.date.accessioned	2020-12-28T10:56:29Z	-
dc.date.available	2020-12-28T10:56:29Z	-
dc.date.issued	2020	-
dc.identifier.citation	Asian Journal of Organic Chemistry	en_US
dc.identifier.other	https://doi.org/10.1002/ajoc.202000560	-
dc.identifier.uri	https://onlinelibrary.wiley.com/doi/10.1002/ajoc.202000560	-
dc.identifier.uri	http://hdl.handle.net/123456789/3427	-
dc.description.abstract	We report the Pd(II)-catalyzed picolinamide-aided ortho-C−H arylation-, alkylation-, and halogenation (sp2 γ−C−H functionalization) of phenylglycinol substrates. Phenylglycinols are remarkable building blocks and have found different applications in synthetic organic and medicinal chemistry. This work is a contribution towards the expansion of the library of phenylglycinol scaffolds and also substrate scope development by using the Pd(II)-catalyzed bidentate directing group picolinamide-aided C−H activation tactic.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley‐VCH GmbH	en_US
dc.subject	C−H activation	en_US
dc.subject	C−H functionalization	en_US
dc.subject	Palladium	en_US
dc.subject	Phenylglycinol	en_US
dc.title	Pd(II)‐catalyzed, Picolinamide‐aided sp2 γ−C−H Functionalization of Phenylglycinol: Access to γ−C−H Arylated, Alkylated and Halogenated Phenylglycinol Scaffolds	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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