Literature DB >> 26357837

Indium(III) Chloride-Catalyzed Isocyanide Insertion Reaction to Construct Complex Spirooxindole.

Yaming Tian1, Lumin Tian1, Xiang He1, Chunju Li1, Xueshun Jia1,2, Jian Li1.   

Abstract

An unusual multiple isocyanide insertion reaction with methyleneindolinone using indium(III) chloride as the catalyst has been disclosed. This strategy allows for the rapid construction of structurally complex spirooxindole in an efficient manner. The present protocol features mild conditions, atom economy, and broad substrate scope.

Entities:  

Year:  2015        PMID: 26357837     DOI: 10.1021/acs.orglett.5b02432

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Unexpected isocyanide-based three-component bicyclization for the stereoselective synthesis of densely functionalized pyrano[3,4-c]pyrroles.

Authors:  Qian Gao; Wen-Juan Hao; Feng Liu; Shu-Jiang Tu; Shu-Liang Wang; Guigen Li; Bo Jiang
Journal:  Chem Commun (Camb)       Date:  2016-01-18       Impact factor: 6.222

2.  New Three-Component Bicyclization Leading to Densely Functionalized Pyrazolo[3,4-d]thiazolo[3,2-a]pyrimidines.

Authors:  Wen-Juan Hao; Peng Zhou; Fei-Yue Wu; Bo Jiang; Shu-Jiang Tu; Guigen Li
Journal:  European J Org Chem       Date:  2016-03-29
  2 in total

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