Selective C–H fluoroalkylation of azines enabled by tailored phosphorus-based reagents

Kanda, Yuzuru; Hong, Seung Youn; Radosevich, Alexander T.

doi:10.1016/j.chempr.2021.05.011

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Selective C–H fluoroalkylation of azines enabled by tailored phosphorus-based reagents : Selective C-H fluoroalkylation of azines enabled by tailored phosphorus-based reagents

DC Field	Value	Language
dc.contributor.author	Kanda, Yuzuru	-
dc.contributor.author	Hong, Seung Youn	-
dc.contributor.author	Radosevich, Alexander T.	-
dc.date.accessioned	2023-05-03T07:46:31Z	-
dc.date.available	2023-05-03T07:46:31Z	-
dc.date.created	2023-05-02	-
dc.date.created	2023-05-02	-
dc.date.issued	2021-06	-
dc.identifier.citation	CHEM, Vol.7 No.6, pp.1420-1422	-
dc.identifier.issn	2451-9294	-
dc.identifier.uri	https://hdl.handle.net/10371/191833	-
dc.description.abstract	The installation of -CF3 or -CF2H groups into compounds can impact important biologically relevant properties. In a recent paper published in Nature, McNally, Paton, and co-workers introduce novel phosphine-based reagents that allow for the conversion of a variety of complex azines through C-H functionalization directly into their fluoroalkylated derivatives.	-
dc.language	영어	-
dc.publisher	CELL PRESS	-
dc.title	Selective C–H fluoroalkylation of azines enabled by tailored phosphorus-based reagents	-
dc.title.alternative	Selective C-H fluoroalkylation of azines enabled by tailored phosphorus-based reagents	-
dc.type	Article	-
dc.identifier.doi	10.1016/j.chempr.2021.05.011	-
dc.citation.journaltitle	CHEM	-
dc.identifier.wosid	000660002500009	-
dc.identifier.scopusid	2-s2.0-85107340145	-
dc.citation.endpage	1422	-
dc.citation.number	6	-
dc.citation.startpage	1420	-
dc.citation.volume	7	-
dc.description.isOpenAccess	Y	-
dc.contributor.affiliatedAuthor	Hong, Seung Youn	-
dc.type.docType	Editorial Material	-
dc.description.journalClass	1	-