Home / Articles / 1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring

1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring

Victor Petrovich Krivopalov 1
Victor Petrovich Krivopalov
, 
Oleg Pavlovich Shkurko 1
Oleg Pavlovich Shkurko
1 N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistryof the Siberian Branch of Russian Academy of Sciences
10.1070/RC2005v074n04ABEH000893
Published 30 November 2004
Communication , Volume 74, Issue 4, 339-379
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Krivopalov V. P., Shkurko O. P. 1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring // Russian Chemical Reviews. 2005. Vol. 74. No. 4. pp. 339-379.
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Krivopalov V. P., Shkurko O. P. 1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring // Russian Chemical Reviews. 2005. Vol. 74. No. 4. pp. 339-379.
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TY - JOUR
DO - 10.1070/RC2005v074n04ABEH000893
UR - https://rcr.colab.ws/publications/10.1070/RC2005v074n04ABEH000893
TI - 1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring
T2 - Russian Chemical Reviews
AU - Krivopalov, Victor Petrovich
AU - Shkurko, Oleg Pavlovich
PY - 2005
DA - 2004/11/30
PB - ANO Editorial Board of the journal Uspekhi Khimii
SP - 339-379
IS - 4
VL - 74
ER -
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@article{2005_Krivopalov,
author = {Victor Petrovich Krivopalov and Oleg Pavlovich Shkurko},
title = {1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring},
journal = {Russian Chemical Reviews},
year = {2005},
volume = {74},
publisher = {ANO Editorial Board of the journal Uspekhi Khimii},
month = {Nov},
url = {https://rcr.colab.ws/publications/10.1070/RC2005v074n04ABEH000893},
number = {4},
pages = {339--379},
doi = {10.1070/RC2005v074n04ABEH000893}
}
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Krivopalov, Victor Petrovich, and Oleg Pavlovich Shkurko. “1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring.” Russian Chemical Reviews, vol. 74, no. 4, Nov. 2005, pp. 339-379. https://rcr.colab.ws/publications/10.1070/RC2005v074n04ABEH000893.
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Abstract

Data on the synthetic routes to substituted 1,2,3-triazoles, including those containing functional groups, based on cyclisation of various nitrogen compounds published during the last 15 years are described. Examples of using new triazole derivatives in agrochemistry, medicine and engineering are given.