Lewis Acid-Promoted Synthesis of 3-Tosylisoindolinone from 3-Hydroxyisoindolinone: Access to Complex Furopyrroloisoindoledione

Authors

  • Anil Kumar Saikia Indian Institute of Technology Guwahati
  • Malay Das Indian Institute of Technology Guwahati
  • Virendra Kumar Indian Institute of Technology Guwahati
  • Pallav Jyoti Arandhara Indian Institute of Technology Guwahati
  • Subhamoy Biswas Indian Institute of Technology Guwahati

DOI:

https://doi.org/10.56042/ijc.v64i12.17877

Abstract

An efficient methodology has been developed for the synthesis of sulfur-functionalized isoindolone scaffold from hydroxyisoindolinone via N-acyliminium ion intermediate using TosMIC and Lewis acid in good to excellent yields. The strategy features mild reaction conditions, broad substrate scope, metal-free reaction method. The protocol has been extended for the synthesis of complex furopyrroloisoindoledione derivatives.

Author Biographies

  • Malay Das, Indian Institute of Technology Guwahati

    Department of Chemistry

  • Virendra Kumar, Indian Institute of Technology Guwahati

    Department of Chemistry

  • Pallav Jyoti Arandhara, Indian Institute of Technology Guwahati

    Department of Chemistry

  • Subhamoy Biswas, Indian Institute of Technology Guwahati

    Department of Chemistry

Published

2025-12-24

How to Cite

Lewis Acid-Promoted Synthesis of 3-Tosylisoindolinone from 3-Hydroxyisoindolinone: Access to Complex Furopyrroloisoindoledione. (2025). Indian Journal of Chemistry (IJC), 64(12), 1133-1143. https://doi.org/10.56042/ijc.v64i12.17877