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Metal-Free Visible-Light-Mediated Transamidation of Ts-Protected Carboxamides: A Green Route to Access Secondary and Tertiary Amides

  • Vishal Singh
  • , Khushbu Rajput
  • , Priya Mahaur
  • , Bobby Jaiswal
  • , Sundaram Singh*
  • , Vandana Srivastava*
  • *Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

Abstract

An unconventional method for synthesizing amides via transamidation of secondary carboxamides, followed by C–N bond activation, is presented. This newly developed process enables the efficient synthesis of highly substituted secondary and tertiary amides. In this work, we introduce a metal-free, catalyst-free, and environmentally friendly synthesis of amides, using Ts-protected secondary carboxamides in combination with amines. This method provides a wide range of substrate compatibility, excellent functional-group tolerance, and uses visible light as a renewable energy source. Additionally, the method is scalable to gram quantities, offering an eco-friendly and efficient alternative for amide synthesis.

Original languageEnglish
Pages (from-to)1739-1750
Number of pages12
JournalSynthesis
Volume58
Issue number15
DOIs
StatePublished - 1 Aug 2026
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2026. Thieme. All rights reserved.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Keywords

  • EDA complex
  • catalyst free
  • scalable
  • transamidation
  • visible-light-mediated

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry

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