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◆ Organic Letters2026-04-21· Chemistry

Red-Light Photoredox C–H Alkylation of Acceptor Heterocycles Enabled by Substoichiometric NADH

Uxía Deus-Lorenzo, Riccardo Di Forti, Alejandro Cadranel, María Tomás‐Gamasa, José L. Mascareñas, Mauro Mato

原始摘要(英文原文)· Original abstract
High Resolution Image Download MS PowerPoint Slide NADH is a key redox mediator in biology and biocatalysis, yet its catalytic use in non-enzymatic synthetic chemistry remains largely unexplored. Here, we show that NADH can act as a substoichiometric reductive quencher in red-light photoredox catalysis, enabling a redox-neutral C(sp 2 )–H alkylation of acceptor heterocycles. This strategy reduces waste and leads to excellent yields and selectivity by suppressing overreduction. The reaction proceeds in air, under mild, aqueous-compatible conditions and operates in biorelevant media, establishing NADH as a cofactor for artificial red-light photoredox catalysis.
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Red-Light Photoredox C–H Alkylation of Acceptor Heterocycles Enabled by Substoichiometric NADH — 科研速览 Science Skim