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May 13, 2026Organic & Biomolecular Chemistry0 citations

One-pot click chemistry using hydrazine as an azide surrogate: easy access to 1,2,3-triazole functionalities

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MSMuzamil SamadMIMohd IrfanRARiyaz Ahmed

Key Points

  • The research focuses on developing a one-pot synthesis method for 1,2,3-triazoles using click chemistry techniques.
  • Utilized phenylhydrazine HCl as an azide surrogate in a one-pot method.
  • Carried out synthesis in PEG-400 and water under copper-catalyzed azide-alkyne cycloaddition (CuAAC) conditions.
  • Eliminated the need for chromatography in the synthesis process.
  • Achieved high yields of 1,2,3-triazoles.
  • Demonstrated broad scope for various substrates.
  • Facilitated late-stage functionalization of compounds.

Abstract

A green, one-pot CuAAC using phenylhydrazine HCl as azide surrogate in PEG-400/H 2 O enables safe, chromatography-free synthesis of 1,2,3-triazoles in high yields with broad scope and late-stage functionalization.

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Cite This Study

Samad et al. (2026) studied this question.

synapsesocial.com/papers/6a03cbfc1c527af8f1ecfe2fhttps://doi.org/10.1039/d6ob00521g
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