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Copper-Catalyzed Stereoselective Radical Phosphono-hydrazonation of Alkynes.
Ogundipe, Olukayode Olamiji; Shoberu, Adedamola; Zou, Jian-Ping.
Affiliation
  • Ogundipe OO; Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Soochow University, 199 Renai Street, Suzhou, Jiangsu 215123, China.
  • Shoberu A; Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Soochow University, 199 Renai Street, Suzhou, Jiangsu 215123, China.
  • Zou JP; Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering, Soochow University, 199 Renai Street, Suzhou, Jiangsu 215123, China.
J Org Chem ; 87(21): 14555-14564, 2022 Nov 04.
Article in En | MEDLINE | ID: mdl-36264682
ABSTRACT
A copper-catalyzed stereoselective phosphono-hydrazonation of terminal alkynes with alkyl carbazates and diarylphosphine oxides is described. This methodology provides facile access to a variety of ß-hydrazonophosphine oxides in satisfactory yields. The reaction proceeds under mild conditions and exhibits good functional group tolerance. A mechanism featuring persulfate-mediated oxidative generation of phosphinoyl radicals and copper-assisted hydrazonation is proposed.

Full text: 1 Database: MEDLINE Language: En Journal: J Org Chem Year: 2022 Type: Article Affiliation country: China

Full text: 1 Database: MEDLINE Language: En Journal: J Org Chem Year: 2022 Type: Article Affiliation country: China