Your browser doesn't support javascript.
loading
Cu-Promoted Divergent Phosphination of Alkynylsulfonium Salts with Diarylphosphines.
Sun, Jinghui; Tong, Hao; Yan, Yifei; Huang, Zhiwei; Chen, Xuanxuan; Huang, Yinhua.
Affiliation
  • Sun J; College of Materials, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China.
  • Tong H; College of Materials, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China.
  • Yan Y; College of Materials, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China.
  • Huang Z; College of Materials, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China.
  • Chen X; College of Materials, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China.
  • Huang Y; College of Materials, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China.
Org Lett ; 26(35): 7414-7418, 2024 Sep 06.
Article in En | MEDLINE | ID: mdl-39189969
ABSTRACT
An efficient copper-promoted divergent phosphination of alkynylsulfonium salts 1 with secondary diarylphosphines 2 that tolerates a wide range of functional groups under mild conditions is reported. The use of excess alkynyl dibenzothiophenium salts (1/2 > 1, mole ratio) enables the phosphination to deliver alkynyl monophosphine products via a C(sp)-P cross-coupling in good to high yields, while the use of excess secondary diarylphosphines (1/2 < 0.5, mole ratio) leads to a type of cis-ethenyl bisphosphine products via sequential stereoselective double phosphination.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2024 Document type: Article Affiliation country: Country of publication: