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volume 91 issue suppl 1

Strategies Towards the Synthesis of N2-Substituted 1,2,3-Triazoles.

Publication typeJournal Article
Publication date2019-02-15
scimago Q2
wos Q3
SJR0.295
CiteScore2.1
Impact factor1.1
ISSN00013765, 16782690
Multidisciplinary
Abstract
The chemistry of 1,2,3-triazoles gained much attention since the discovery of the copper catalyzed Alkyne-azide cycloaddition (CuAAC) reaction which delivers exclusively the 1,4-regioisomer in high yields. On the other hand there is still no universal methodology capable of delivering the N2 substituted regioisomer. The unique properties of these N2-substituted 1,2,3-triazoles have stimulated synthetic efforts on the developments of methodologies capable of delivering it in high yield and selectivity. These efforts are the subject of the presented review.
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SOUZA R. O. M. D., Miranda L. S. M. Strategies Towards the Synthesis of N2-Substituted 1,2,3-Triazoles. // Anais da Academia Brasileira de Ciencias. 2019. Vol. 91. No. suppl 1.
GOST all authors (up to 50) Copy
SOUZA R. O. M. D., Miranda L. S. M. Strategies Towards the Synthesis of N2-Substituted 1,2,3-Triazoles. // Anais da Academia Brasileira de Ciencias. 2019. Vol. 91. No. suppl 1.
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RIS Copy
TY - JOUR
DO - 10.1590/0001-3765201820180751
UR - https://doi.org/10.1590/0001-3765201820180751
TI - Strategies Towards the Synthesis of N2-Substituted 1,2,3-Triazoles.
T2 - Anais da Academia Brasileira de Ciencias
AU - SOUZA, RODRIGO OCTÁVIO M.A. DE
AU - Miranda, Leandro S M
PY - 2019
DA - 2019/02/15
PB - Academia Brasileira de Ciencias
IS - suppl 1
VL - 91
PMID - 30785471
SN - 0001-3765
SN - 1678-2690
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2019_SOUZA,
author = {RODRIGO OCTÁVIO M.A. DE SOUZA and Leandro S M Miranda},
title = {Strategies Towards the Synthesis of N2-Substituted 1,2,3-Triazoles.},
journal = {Anais da Academia Brasileira de Ciencias},
year = {2019},
volume = {91},
publisher = {Academia Brasileira de Ciencias},
month = {feb},
url = {https://doi.org/10.1590/0001-3765201820180751},
number = {suppl 1},
doi = {10.1590/0001-3765201820180751}
}