Electrochemical Oxidative Coupling between Benzylic C(sp3)-H and N-H of Secondary Amines: Rapid Synthesis of α-Amino α-Aryl Esters

Full metadata record

DC Field	Value	Language
dc.contributor.author	Nagare Y.K.	en_US
dc.contributor.author	Shah I.A.	en_US
dc.contributor.author	Yadav J.	en_US
dc.contributor.author	Pawar A.P.	en_US
dc.contributor.author	Choudhary R.	en_US
dc.contributor.author	Chauhan P.	en_US
dc.contributor.author	Kumar I.	en_US
dc.date.accessioned	2023-11-30T08:44:51Z	-
dc.date.available	2023-11-30T08:44:51Z	-
dc.date.issued	2021	-
dc.identifier.issn	0022-3263	-
dc.identifier.other	EID(2-s2.0-85110982607)	-
dc.identifier.uri	https://dx.doi.org/10.1021/acs.joc.1c00944	-
dc.identifier.uri	http://localhost:8080/xmlui/handle/123456789/664	-
dc.description.abstract	An intermolecular electrochemical coupling between the benzylic C(sp3)-H bond and various secondary amines is reported. The electronic behavior of two electronically rich units viz the α-position of α-aryl acetates and amines was engineered electrochemically, thus facilitating their reactivity for the direct access of α-amino esters. A series of acyclic/cyclic secondary amines and α-aryl acetates were tested to furnish the corresponding α-amino esters with high yields (up to 92%) under mild conditions. © 2021 American Chemical Society.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.source	Journal of Organic Chemistry	en_US
dc.title	Electrochemical Oxidative Coupling between Benzylic C(sp3)-H and N-H of Secondary Amines: Rapid Synthesis of α-Amino α-Aryl Esters	en_US
dc.type	Journal Article	en_US
Appears in Collections:	Journal Article