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Construction of Bispirooxindole Heterocycles via Palladium-Catalyzed Ring-Opening Formal [3 + 2]-Cycloaddition of Spirovinylcyclopropyl Oxindole and 3-Oxindole Derivatives.
Xiao, Jun-An; Li, Yu-Chun; Luo, Zhi-Jin; Cheng, Xiu-Liang; Deng, Zhi-Xiong; Chen, Wen-Qiang; Su, Wei; Yang, Hua.
Afiliação
  • Xiao JA; Guangxi Key Laboratory of Natural Polymer Chemistry and Physics , Nanning Normal University , Nanning 530001 , P.R. China.
  • Li YC; Guangxi Key Laboratory of Natural Polymer Chemistry and Physics , Nanning Normal University , Nanning 530001 , P.R. China.
  • Luo ZJ; Guangxi Key Laboratory of Natural Polymer Chemistry and Physics , Nanning Normal University , Nanning 530001 , P.R. China.
  • Cheng XL; Guangxi Key Laboratory of Natural Polymer Chemistry and Physics , Nanning Normal University , Nanning 530001 , P.R. China.
  • Deng ZX; College of Chemistry and Chemical Engineering , Central South University , Changsha 410083 , P.R. China.
  • Chen WQ; Guangxi Key Laboratory of Natural Polymer Chemistry and Physics , Nanning Normal University , Nanning 530001 , P.R. China.
  • Su W; Guangxi Key Laboratory of Natural Polymer Chemistry and Physics , Nanning Normal University , Nanning 530001 , P.R. China.
  • Yang H; College of Chemistry and Chemical Engineering , Central South University , Changsha 410083 , P.R. China.
J Org Chem ; 84(4): 2297-2306, 2019 Feb 15.
Article em En | MEDLINE | ID: mdl-30632746
A palladium-catalyzed ring-opening oxo-formal [3 + 2]-cycloaddition reaction of novel donor-acceptor spirovinylcyclopropyl oxindole with 3-oxindole is described. The developed protocol provides facile access to oxo-bispirooxindole derivatives in good yields (up to 82% yield) with excellent diastereoselectivities (up to 20:1 dr).

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Org Chem Ano de publicação: 2019 Tipo de documento: Article