C-H imidation: a distinct perspective of C-N bond formation

dc.contributor.author Rit, Raja K.
dc.contributor.author Shankar, Majji
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T09:56:07Z
dc.date.available 2022-03-27T09:56:07Z
dc.date.issued 2017-01-01
dc.description.abstract The direct imidation strategy proficiently constructs C-N bonds and creates the useful amine functional group in the molecular template. This review briefly discusses the synthetic methods developed for the direct imidation of unactivated C(sp2/sp3/sp)-H bonds. Transition-metal catalysts, metal-free processes, and/or photo-induced methods are invariably employed for accomplishing C-H imidation transformations. The contents summarized herein would benefit the research community to use the C-H imidation reactions for broad synthetic applications and to unravel novel C-N bond forming processes.
dc.identifier.citation Organic and Biomolecular Chemistry. v.15(6)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c6ob02162j
dc.identifier.uri http://xlink.rsc.org/?DOI=C6OB02162J
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13452
dc.title C-H imidation: a distinct perspective of C-N bond formation
dc.type Journal. Review
dspace.entity.type
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