Microwave-Assisted Synthesis of Fine Chemicals – Triazoles

Shainaz Landge, Charles Melvin, Asher Pence

Research output: Contribution to book or proceedingChapterpeer-review

Abstract

Microwave irradiation has been used as a prominent form of energy resource, shown to maximize efficiency by speeding up reactions. The microwave-assisted organic synthesis (MAOS) increases yields with shorter reaction times. Triazoles, one of the fine chemicals, is generally synthesized via “click chemistry” with azides and alkynes as starting materials. Through one step synthesis, it provides ease and accessibility to diverse libraries of compounds and improves atom economy. In particular, the microwave assisted click reaction provides one of the known reaction pathways to obtain biologically active triazoles in a short time compared to conventional methods. The reaction can result in 1,2,3-triazoles and 1,2,4-triazoles with high yields at the 1,4 or 1, 3- di-substituted positions. This chapter focuses on the recent advances (last decade) of this microwave assisted organic reactions resulting in triazoles.

Original languageEnglish
Title of host publicationEncyclopedia of Green Chemistry, First Edition
Subtitle of host publicationVolume 1-4
PublisherElsevier
PagesV2:270-V2:287
Volume2
ISBN (Electronic)9780443157424
ISBN (Print)9780443289231
DOIs
StatePublished - Feb 28 2025

Publication series

NameEncyclopedia of Green Chemistry, First Edition: Volume 1-4
Volume2

Scopus Subject Areas

  • General Chemistry

Keywords

  • 1,2,3-Triazoles
  • 1,2,4-Triazoles
  • Alkyne
  • Azide
  • Green synthesis
  • Microwave irradiation

Fingerprint

Dive into the research topics of 'Microwave-Assisted Synthesis of Fine Chemicals – Triazoles'. Together they form a unique fingerprint.

Cite this