Green Chemistry, Год журнала: 2024, Номер 27(3), С. 566 - 572
Опубликована: Дек. 6, 2024
An atom-economical and sustainable electrochemically driven triarylamine-catalyzed dehydrogenative phosphorylation coupling was reported.
Язык: Английский
Green Chemistry, Год журнала: 2024, Номер 27(3), С. 566 - 572
Опубликована: Дек. 6, 2024
An atom-economical and sustainable electrochemically driven triarylamine-catalyzed dehydrogenative phosphorylation coupling was reported.
Язык: Английский
Chinese Journal of Chemistry, Год журнала: 2025, Номер unknown
Опубликована: Март 20, 2025
Comprehensive Summary Herein, it is reported that the aryl radicals derived from thianthrenium salts are used as coupling partner in arylation reactions of isocyanides, simultaneously initiators for formation alkyl and phosphoryl ethers diarylphosphine oxides. This cascade cyclization reaction leads to diverse arylated, alkylated phosphorylated heteroaromatic compounds. Notably, this transformation can be achieved without aid metals or photocatalysts, exhibiting a wide substrate applicability operational simplicity. Mechanistic studies suggest involvement radical processes electron donor‐acceptor (EDA) complexes transformation.
Язык: Английский
Процитировано
0Organic Letters, Год журнала: 2024, Номер unknown
Опубликована: Окт. 30, 2024
Herein, we report a novel and practical strategy for alkyl sulfonium salts mediating radical thiocyanohydroxylation of alkenes. This reaction features metal-free mild conditions, generation noncarbon radicals from the readily available salts, easy handling, excellent functional group compatibility. A diverse range activated unactivated alkenes worked well to deliver various β-thiocyanato alcohols.
Язык: Английский
Процитировано
0Green Chemistry, Год журнала: 2024, Номер 27(3), С. 566 - 572
Опубликована: Дек. 6, 2024
An atom-economical and sustainable electrochemically driven triarylamine-catalyzed dehydrogenative phosphorylation coupling was reported.
Язык: Английский
Процитировано
0