4.5 Review

Recent Developments in Azide-Free Synthesis of 1,2,3-Triazoles

Journal

CHINESE JOURNAL OF CHEMISTRY
Volume 35, Issue 12, Pages 1797-1807

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cjoc.201700459

Keywords

1; 2; 3-triazoles; azide-free; hydrazones; diazo compounds; nitrogen heterocycles

Funding

  1. National Natural Science Foundation of China [21602202]
  2. Science Foundation of Zhejiang Sci-Tech University [15062092-Y, 1206820-Y, 1206821-Y]
  3. Zhejiang Provincial Top Key Academic Discipline of Chemical Engineering and Technology of Zhejiang Sci-Tech University

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1,2,3-Triazoles, as one of the most significant nitrogen-containing heterocycles due to their extensive use in biology, material science and organic synthesis, have aroused great interest. 1,2,3-Triazoles are commonly synthesized by metal-catalyzed azide-alkyne cycloaddition and organocatalytic azide-carbonyl cycloaddition, which indispensably employ the toxic and potentially explosive azides. The azide-free synthetic approaches provide a powerful and straightforward alternative to the assembly of diverse 1,2,3-triazoles without the use of azides. In this review, we summarize the recent development of the construction of 1,2,3-triazoles under azide-free conditions.

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