Phenylboronic acid/CuSO4 as an efficient catalyst for the synthesis of 1,4-disubstituted-1,2,3-triazoles from terminal acetylenes and alkyl azides

José Emilio De La Cerda-Pedro, Susana Rojas-Lima, Rosa Santillan, Heraclio López-Ruiz

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

The synthesis of 1,4-disubstituted-1,2,3-triazoles from alkyl azides and terminal alkynes at room temperature and under microwave heating was attained using Cu(I), generated in-situ from copper(II) sulfate and phenylboronic acid, as catalyst. Twelve new triazoles were obtained in moderate to good yields (53-98%), and the products were obtained by crystallization from the mixture reaction without further purification.

Original languageEnglish
Pages (from-to)130-136
Number of pages7
JournalJournal of the Mexican Chemical Society
Volume59
Issue number2
StatePublished - 1 Apr 2015
Externally publishedYes

Keywords

  • CuSO4
  • Microwave irradiation
  • Phenylboronic acid
  • Triazoles

Fingerprint

Dive into the research topics of 'Phenylboronic acid/CuSO4 as an efficient catalyst for the synthesis of 1,4-disubstituted-1,2,3-triazoles from terminal acetylenes and alkyl azides'. Together they form a unique fingerprint.

Cite this