4.8 Article

Decarboxylative Elimination of N-Acyl Amino Acids via Photoredox/Cobalt Dual Catalysis

期刊

ACS CATALYSIS
卷 8, 期 12, 页码 11801-11806

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.8b03282

关键词

decarboxylative elimination; enamides; enecarbamates; photoredox/cobalt dual catalysis

资金

  1. National Science Foundation [CHE-1800147]
  2. Kansas Bioscience Authority Rising Star program
  3. NSF Academic Research Infrastructure Grant [9512331]
  4. NIH Shared Instrumentation Grant [S10RR024664]
  5. NSF Major Research Instrumentation Grant [0320648]
  6. NSF-MRI grant [CHE-0923449]
  7. Div Of Biological Infrastructure
  8. Direct For Biological Sciences [9512331] Funding Source: National Science Foundation

向作者/读者索取更多资源

A dual-catalytic strategy for the synthesis of enamides and enecarbamates directly from easily accessible and inexpensive amino acids has been realized. This mild and efficient protocol makes use of an organic photoredox catalyst and a cobaloxime catalyst to achieve decarboxylative elimination using hydrogen evolution to drive the oxidation. Thus, the reaction occurs without a stoichiometric oxidant or the forcing conditions previously employed in attempts to achieve similar eliminations.

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