Synthesis 2017; 49(16): 3609-3618
DOI: 10.1055/s-0036-1588820
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of 1-Alkyl-3-(2-oxo-2-aryl/alkyl-ethyl)indolin-2-ones through Gold/Brønsted Acid Relay Actions: Observation of Selective C=C Bond Cleavage of Enaminones

Autoren

  • Yulei Zhao

    Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 500 Dongchuan Road, Shanghai 200241, P. R. of China   eMail: yzli@chem.ecnu.edu.cn
  • Yang Yuan

    Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 500 Dongchuan Road, Shanghai 200241, P. R. of China   eMail: yzli@chem.ecnu.edu.cn
  • Lingkai Kong

    Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 500 Dongchuan Road, Shanghai 200241, P. R. of China   eMail: yzli@chem.ecnu.edu.cn
  • Fangfang Zhang

    Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 500 Dongchuan Road, Shanghai 200241, P. R. of China   eMail: yzli@chem.ecnu.edu.cn
  • Yanzhong Li*

    Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 500 Dongchuan Road, Shanghai 200241, P. R. of China   eMail: yzli@chem.ecnu.edu.cn

We thank the National Natural Science Foundation of China (Grant No. 21272074) and the Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT) for financial support.
Weitere Informationen

Publikationsverlauf

Received: 13. März 2017

Accepted after revision: 01. April 2017

Publikationsdatum:
09. Mai 2017 (online)


Graphical Abstract

Abstract

A novel gold(I)/Brønsted acid sequential catalyzed/promoted procedure to synthesize 1-alkyl-3-(2-oxo-2-aryl/alkyl-ethyl)indolin-2-ones under mild reaction conditions is developed. This methodology is realized by relay actions of gold and a Brønsted acid in a one-pot multistep manner. The gold(I)-catalyzed chemoselective C(sp2)-H functionalization of enaminones and Brønsted acid promoted cleavage of the C=C bond are integrated effectively. Based on the results of control experiments and ESI-MS analysis, a possible reaction mechanism is proposed.

Supporting Information