| Literature DB >> 32853417 |
Daniel Francis1, Adam Nelson1,2, Stephen P Marsden1.
Abstract
3-Amino-substituted saturated nitrogen heterocycles are an important subclass of β-diamines, appearing in a number of clinical agents. Herein, we report a unified approach to these products based upon the regioselective photoredox-mediated hydroamination of enecarbamates. The amine coupling partner can encompass diverse amine types under a single set of reaction conditions, including primary alkyl amines, ammonia, aryl and heteroaryl amines, and N-H heterocycles. The method enables the synthesis of a wide range of pharmaceutically relevant building blocks.Entities:
Keywords: (hetero)aromatic amine; ammonia; hydroamination; medicinal chemistry toolkit; photoredox
Year: 2020 PMID: 32853417 PMCID: PMC7756410 DOI: 10.1002/chem.202003562
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236