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Additive-Controlled Divergent Synthesis of Amides and Ketones via Ni/Photoredox-Catalyzed Deoxygenative Functionalization of Alcohols

Research output: Journal article publication › Journal article › Academic research › peer-review

Abstract

Amides and ketones are essential carbonyl compounds with widespread applications in pharmaceuticals, materials science, and synthetic chemistry. Herein, we present a Ni/photoredox dual-catalyzed strategy for the divergent synthesis of amides and ketones from isocyanates and alcohols. This transformation is facilitated by N-heterocyclic carbene (NHC)-mediated activation of alcohols and is selectively controlled by the choice of additive: NaOAc promotes amide formation, whereas nBu4NPO4H2 directs the reaction toward ketone synthesis. This approach offers a versatile and practical route to access amides and ketones from readily available alcohol feedstocks.

Original languageEnglish
Pages (from-to)6179-6188
Number of pages10
JournalJACS Au
Volume5
Issue number12
DOIs
Publication statusPublished - 20 Nov 2025

Keywords

  • additive-controlled selectivity
  • alcohol
  • amide
  • isocyanate
  • ketone
  • Ni/photoredox dual catalysis

ASJC Scopus subject areas

  • Analytical Chemistry
  • Chemistry (miscellaneous)
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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