| Literature DB >> 28339212 |
Bryan J Simmons1, Marie Hoffmann1, Jaeyeon Hwang1, Moritz K Jackl1, Neil K Garg1.
Abstract
The nickel-catalyzed reduction of secondary and tertiary amides to give amine products is reported. The transformation is tolerant of extensive variation with respect to the amide substrate, proceeds in the presence of esters and epimerizable stereocenters, and can be used to achieve the reduction of lactams. Moreover, this methodology provides a simple tactic for accessing medicinally relevant α-deuterated amines.Entities:
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Year: 2017 PMID: 28339212 PMCID: PMC5476940 DOI: 10.1021/acs.orglett.7b00683
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005