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