Literature DB >> 22735645

Copper-catalyzed domino coupling reaction: an efficient method to synthesize oxindoles.

Jen-Chieh Hsieh1, An-Yi Cheng, Jun-Hao Fu, Ting-Wei Kang.   

Abstract

An efficient and novel procedure for a copper catalyzed domino coupling reaction has been developed, which afforded various oxindoles in good to excellent yields with tolerance of various substituents. In addition, this method could be applied to synthesize horsfiline and coerulescine in few steps with high total yields.

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Year:  2012        PMID： 22735645     DOI： 10.1039/c2ob26110c

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN： 1477-0520            Impact factor:   3.876


  3 in total

Review 1.  Literature Survey and Further Studies on the 3-Alkylation of N-Unprotected 3-Monosubstituted Oxindoles. Practical Synthesis of N-Unprotected 3,3-Disubstituted Oxindoles and Subsequent Transformations on the Aromatic Ring.

Authors:  Eszter Kókai; Gyula Simig; Balázs Volk
Journal:  Molecules       Date:  2016-12-26       Impact factor: 4.411

2.  Alcohols as Substrates and Solvents for the Construction of 3-Alkoxylated-2-Oxindoles by Direct Alkoxylation of 3-Halooxindoles.

Authors:  Bing Lin; Zhi-Yong Chen; Huan-Huan Liu; Qi-Di Wei; Ting-Ting Feng; Ying Zhou; Can Wang; Xiong-Li Liu; Wei-Cheng Yuan
Journal:  Molecules       Date:  2017-05-13       Impact factor: 4.411

3.  Electrochemical Umpolung C-H Functionalization of Oxindoles.

Authors:  Miryam Pastor; Marie Vayer; Harald Weinstabl; Nuno Maulide
Journal:  J Org Chem       Date:  2021-12-28       Impact factor: 4.354
  3 in total

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