Interrupted Michael Reaction: Sulfophosphinoylation of α,β-Unsaturated Ketones Catalyzed by Phosphine DOI
Xiaohong Wei,

Ya-Wen Xue,

Xuan Liu

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(22), С. 16564 - 16570

Опубликована: Окт. 31, 2024

An efficient method for phosphine-catalyzed sulfophosphinoylation of α,β-unsaturated ketones synthesis allylic organophosphorus compounds has been reported, in which acting as zwitterions react with electrophiles and nucleophiles to form a C-P bond C-O obtain high regio- stereoselectivity moderate excellent yields.

Язык: Английский

Silver-Catalyzed 1,2-Thiosulfonylation of Alkenes: Development of a Nucleophilic d3-Methylthiolating Reagent DOI

Zhiyong Ye,

Yan Zhang,

Guofang Guo

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер unknown

Опубликована: Сен. 25, 2024

Development of robust

Язык: Английский

Процитировано

0

Interrupted Michael Reaction: Sulfophosphinoylation of α,β-Unsaturated Ketones Catalyzed by Phosphine DOI
Xiaohong Wei,

Ya-Wen Xue,

Xuan Liu

и другие.

The Journal of Organic Chemistry, Год журнала: 2024, Номер 89(22), С. 16564 - 16570

Опубликована: Окт. 31, 2024

An efficient method for phosphine-catalyzed sulfophosphinoylation of α,β-unsaturated ketones synthesis allylic organophosphorus compounds has been reported, in which acting as zwitterions react with electrophiles and nucleophiles to form a C-P bond C-O obtain high regio- stereoselectivity moderate excellent yields.

Язык: Английский

Процитировано

0