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Construction of gem-Difluoroenol Esters through Catalytic O-Selective Addition of Difluoroenoxysilanes to Ketenes.
Shi, Yang; Pan, Bo-Wen; He, Jun-Xiong; Zhou, Ying; Zhou, Jian; Yu, Jin-Sheng.
Afiliación
  • Shi Y; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • Pan BW; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • He JX; Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China.
  • Zhou Y; College of Pharmacy, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • Zhou J; Shanghai Engineering Research Center of Molecular Therapeutics and New Drug Development, School of Chemistry and Molecular Engineering, East China Normal University, Shanghai 200062, China.
  • Yu JS; State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai 200032, China.
J Org Chem ; 86(11): 7797-7805, 2021 06 04.
Article en En | MEDLINE | ID: mdl-34000179
ABSTRACT
The O-site reactivity of difluoroenoxysilanes is disclosed for the first time, which enabled the direct construction of versatile gem-difluoroalkenes through an unprecedented highly efficient addition reaction with ketenes. A series of valuable gem-difluoroenol esters were achieved in good to excellent yields. The synthetic versatility of this protocol is further demonstrated by the gram-scale synthesis and good functional group tolerance.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ésteres / Cetonas Idioma: En Revista: J Org Chem Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ésteres / Cetonas Idioma: En Revista: J Org Chem Año: 2021 Tipo del documento: Article País de afiliación: China