Photoredox-Catalyzed Direct C(sp2)–H Difluoromethylation of Hydrazones with Difluoromethyltriphenylphosphonium Salt via Aminyl Radical/Polar Crossover DOI

Xiao‐Di Wu,

Wang Li,

Ji‐Yu Tao

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Апрель 10, 2025

This study describes an efficacious and generally applicable synthetic strategy for the incorporation of biologically physiologically prominent difluoromethyl entity into synthetically crucial hydrazone scaffolds with bench-stable easily accessible difluoromethyltriphenylphosphonium bromide. The broad substrate scope, excellent functional group compatibility, feasibility step atom economical one-pot manipulation, environmentally benign mild reaction conditions rendered this methodology efficient tool preparation pharmaceutically fluorine-containing imino compounds.

Язык: Английский

Photocatalytically switchable chemoselective difluoramidation of olefins for the synthesis of diversified difluoro-γ-lactams DOI

Tian-Zheng Cao,

Cai-Jian Nie,

Jing Li

и другие.

Chemical Communications, Год журнала: 2025, Номер unknown

Опубликована: Янв. 1, 2025

This study demonstrates a visible-light-driven intramolecular alkene difluorination enabling Heck-type coupling, hydrofluoramidation, and difunctionalization. Diverse difluoro-γ-lactams were synthesized with high selectivity substrate generality.

Язык: Английский

Процитировано

0

Photoredox-Catalyzed Direct C(sp2)–H Difluoromethylation of Hydrazones with Difluoromethyltriphenylphosphonium Salt via Aminyl Radical/Polar Crossover DOI

Xiao‐Di Wu,

Wang Li,

Ji‐Yu Tao

и другие.

Organic Letters, Год журнала: 2025, Номер unknown

Опубликована: Апрель 10, 2025

This study describes an efficacious and generally applicable synthetic strategy for the incorporation of biologically physiologically prominent difluoromethyl entity into synthetically crucial hydrazone scaffolds with bench-stable easily accessible difluoromethyltriphenylphosphonium bromide. The broad substrate scope, excellent functional group compatibility, feasibility step atom economical one-pot manipulation, environmentally benign mild reaction conditions rendered this methodology efficient tool preparation pharmaceutically fluorine-containing imino compounds.

Язык: Английский

Процитировано

0