Title:
Facile Metal-Free Synthesis of Phenanthridines by SN2′ Reaction/C–H Functionalization/Aromatization through the Reaction of Morita–Baylis–Hillman Acetates with Nitroalkanes

Simple item page
dc.contributor.authorTanu Gupta
dc.contributor.authorJay Bahadur Singh
dc.contributor.authorKalpana Mishra
dc.contributor.authorBiswajit Maiti
dc.contributor.authorRadhey M. Singh
dc.date.accessioned2026-02-07T08:47:05Z
dc.date.issued2018
dc.description.abstractA simple, highly efficient, and regioselective synthesis of functionalized phenanthridines by the reaction of MBH acetates of 2-chloroquinoline-3-carbaldehydes with nitroalkanes is described. The reaction involves an SN2′ reaction/C–H functionalization/aromatization process. The method is simple and proceeds under mild conditions under an air atomosphere to give phenanthridines in good to excellent yields. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
dc.identifier.doi10.1002/ejoc.201701574
dc.identifier.issn1434193X
dc.identifier.urihttps://doi.org/10.1002/ejoc.201701574
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/32411
dc.publisherWiley-VCH Verlag
dc.subjectCyclization
dc.subjectDomino reactions
dc.subjectElimination
dc.subjectFused-ring systems
dc.subjectNitrogen heterocycles
dc.titleFacile Metal-Free Synthesis of Phenanthridines by SN2′ Reaction/C–H Functionalization/Aromatization through the Reaction of Morita–Baylis–Hillman Acetates with Nitroalkanes
dc.typePublication
dspace.entity.typeArticle

Files

Collections

2018
An Initiative by BHU – Central Library
Powered by Dspace