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C-O Coupling/[4+2] Cycloaddition Tandem Reactions via Oxidative Dearomatization of BINOLs: Access to Bridged Polycyclic Compounds.
Liu, Hao; Gong, Zi-Rong; Lin, Meng-Ling; Luo, Wen; Xu, Yan-Jun; Dong, Lin.
Afiliación
  • Liu H; College of Chemistry and Material Science, Sichuan Normal University, Chengdu, Sichuan 610066, China.
  • Gong ZR; Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, Chi
  • Lin ML; College of Chemistry and Material Science, Sichuan Normal University, Chengdu, Sichuan 610066, China.
  • Luo W; Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, Chi
  • Xu YJ; Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, Chi
  • Dong L; College of Chemistry and Material Science, Sichuan Normal University, Chengdu, Sichuan 610066, China.
J Org Chem ; 88(6): 3916-3926, 2023 Mar 17.
Article en En | MEDLINE | ID: mdl-36849248
ABSTRACT
Intramolecular C-H activation/C-O coupling, dearomatization, and [4+2] cycloaddition of BINOL units have been well developed in a one-pot approach with maleimide derivatives as the dienophiles. This tandem catalytic system generates a variety of functionalized bridged polycyclic products in a step-economical manner, which greatly enriches the modification methods and strategies for the BINOL skeletons.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2023 Tipo del documento: Article País de afiliación: China