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Organocatalytic Asymmetric α-Sulfenylation of 2-Substituted Indolin-3-ones: A Strategy for the Synthesis of Chiral 2,2-Disubstituted Indole-3-ones with S- and N-Containing Heteroquaternary Carbon Stereocenter.
Zhao, Yong-Long; Fei, Xing-Hai; Tang, Yong-Qin; Xu, Peng-Fei; Yang, Fen-Fen; He, Bin; Fu, Xiao-Zhong; Yang, Yuan-Yong; Zhou, Meng; Mao, Yuan-Hu; Dong, Yong-Xi; Li, Chun.
Afiliação
  • Zhao YL; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Fei XH; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Tang YQ; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Xu PF; State Key Laboratory of Applied Organic Chemistry and College of Chemistry & Chemical Engineering , Lanzhou University , Lanzhou 730000 , P. R. China.
  • Yang FF; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • He B; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Fu XZ; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Yang YY; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Zhou M; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Mao YH; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Dong YX; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
  • Li C; State Key Laboratory of Functions and Applications of Medicinal Plants, School of Pharmacy, Engineering Research Center for the Development and Application of Ethnic Medicine and TCM (Ministry of Education) , Guizhou Medical University , Guiyang 550004 , P. R. China.
J Org Chem ; 84(12): 8168-8176, 2019 06 21.
Article em En | MEDLINE | ID: mdl-31192597
ABSTRACT
An organocatalytic asymmetric α-sulfenylation of 2-substituted indolin-3-ones with N-(alkylthio or arylthio)succinimides has been developed for the first time using Cinchona-derived squaramide as the catalyst. Various chiral 2,2-disubstituted indole-3-ones with S- and N-containing heteroquaternary carbon stereocenters were obtained with up to 98% yield and 99% ee.

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

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