Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Research Article

Synthesis of Novel 1,4-Substituted 1,2,3-Triazoles by Water-Soluble (Salicyladimine) 2Cu Complex Catalyzed Azide-Alkyne Cycloaddition in Water

Author(s): Yang Liu, Ping Liu*, Yan Liu and Yu Wei*

Volume 14, Issue 8, 2017

Page: [557 - 565] Pages: 9

DOI: 10.2174/1570178614666170609072912

Price: $65

Abstract

Background: 1,2,3-Triazoles represent an important structural motif frequently found in organic chemistry, biological science, medicinal chemistry, and material science. Thus, the synthesis of novel 1,2,3-triazoles derivatives by an efficient method has attracted considerable attention.

Methods: In this paper, we developed a simple and efficient azidation system of biphenyl tosylhydrazones with sodium azide. A series of new 4-(1-azidoethyl)-1,1'-biphenyl derivatives were prepared by the metalfree reductive reaction and further reacted with aryl acetylenes to afford novel 1,4-substituted 1,2,3- triazoles by water-soluble (salicyladimine)2Cu complex catalyzed azide-alkyne cycloaddition in water.

Results: The desired 1,4-substituted 1,2,3-triazoles were obtained in 27-94% yields in pure water without any organic solvent or phase transfer agents.

Conclusion: The catalytic system presented here enables the use of easily accessible starting materials and good functional group tolerance.

Keywords: 1, 2, 3-triazoles, (salicyladimine)2Cu complex, azide-alkyne cycloaddition, water, metal-free reductive reaction, functional group.

Graphical Abstract


Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy