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

dc.contributor.authorKumar, Indresh
dc.date.accessioned2024-09-12T09:34:36Z
dc.date.available2024-09-12T09:34:36Z
dc.date.issued2021-06
dc.description.abstractAn 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.en_US
dc.identifier.urihttps://pubs.acs.org/doi/full/10.1021/acs.joc.1c00944
dc.identifier.urihttps://dspace.bits-pilani.ac.in/xmlui/handle/123456789/15552
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectAminesen_US
dc.subjectFossil fuelsen_US
dc.subjectOrganic compoundsen_US
dc.subjectPurificationen_US
dc.titleElectrochemical Oxidative Coupling Between Benzylic C(sp3)–H and N–H of Secondary Amines: Rapid Synthesis of α-Amino α-Aryl Estersen_US
dc.typeArticleen_US

Files

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: