Literature DB >> 32853417

Synthesis of β-Diamine Building Blocks by Photocatalytic Hydroamination of Enecarbamates with Amines, Ammonia and N-H Heterocycles.

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.
© 2020 The Authors. Published by Wiley-VCH GmbH.

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


  30 in total

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8.  Enantioselective Hydroamination of Alkenes with Sulfonamides Enabled by Proton-Coupled Electron Transfer.

Authors:  Casey B Roos; Joachim Demaerel; David E Graff; Robert R Knowles
Journal:  J Am Chem Soc       Date:  2020-03-20       Impact factor: 15.419

Review 9.  The Chemistry of Vicinal Diamines.

Authors:  Denis Lucet; Thierry Le Gall; Charles Mioskowski
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10.  Catalytic Olefin Hydroamidation Enabled by Proton-Coupled Electron Transfer.

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  1 in total

1.  Synthesis of β-Diamine Building Blocks by Photocatalytic Hydroamination of Enecarbamates with Amines, Ammonia and N-H Heterocycles.

Authors:  Daniel Francis; Adam Nelson; Stephen P Marsden
Journal:  Chemistry       Date:  2020-10-07       Impact factor: 5.236

  1 in total

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