Difunctionalization of Alkenes toward 3,3-Disubstituted and Dihydrobenzoindolines by Using an Imidazolylidene Palladacyclic Catalyst DOI

Dong Lin,

Hanxiao Yang,

Yue Chen

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Март 6, 2025

The synthesis of valuable 2a,3-dihydrobenzo[cd]indolines was successfully achieved by combining IPr-Pdcycle-OxaNaphthyl-catalyzed cross-coupling and proton-induced hydroarylation in a one-pot method. In situ-generated alkynyl-functionalized 3,3-disubstituted indolines were proved as the key intermediate, bearing broad scope substrates with diverse functional groups electronic properties.

Язык: Английский

Recent advances on electrochemical generation of sulfonyl radical triggered cyclization of alkene/alkynes DOI

Jiaqing Shao,

Jiang Liu, Haibo Mei

и другие.

Tetrahedron, Год журнала: 2025, Номер 173, С. 134467 - 134467

Опубликована: Янв. 12, 2025

Язык: Английский

Процитировано

1
Difunctionalization of Alkenes toward 3,3-Disubstituted and Dihydrobenzoindolines by Using an Imidazolylidene Palladacyclic Catalyst DOI

Dong Lin,

Hanxiao Yang,

Yue Chen

и другие.

The Journal of Organic Chemistry, Год журнала: 2025, Номер unknown

Опубликована: Март 6, 2025

The synthesis of valuable 2a,3-dihydrobenzo[cd]indolines was successfully achieved by combining IPr-Pdcycle-OxaNaphthyl-catalyzed cross-coupling and proton-induced hydroarylation in a one-pot method. In situ-generated alkynyl-functionalized 3,3-disubstituted indolines were proved as the key intermediate, bearing broad scope substrates with diverse functional groups electronic properties.

Язык: Английский

Процитировано

0