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 language | English |
|---|---|
| Pages (from-to) | 6179-6188 |
| Number of pages | 10 |
| Journal | JACS Au |
| Volume | 5 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 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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