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May 9, 2026Synthesis0 citations

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

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VSVishal SinghKRKhushbu RajputPMPriya Mahaur

Key Points

  • To develop a metal-free and environmentally friendly method for synthesizing secondary and tertiary amides via transamidation.
  • Utilized Ts-protected secondary carboxamides and amines for transamidation
  • Employs visible light as an energy source for the reaction
  • Demonstrated scalability to gram quantities
  • Achieved efficient synthesis of highly substituted secondary and tertiary amides
  • Showed excellent functional group tolerance and wide substrate compatibility
  • Provided an eco-friendly alternative for amide synthesis without catalysts

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, it is scalable to gram quantities, offering an eco-friendly and efficient alternative for amide synthesis.

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Cite This Study

Singh et al. (2026) studied this question.

synapsesocial.com/papers/69fed17eb9154b0b82878e52https://doi.org/10.1055/a-2869-6243
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