TY - JOUR
T1 - Biological importance and synthesis of 1,2,3-triazole derivatives
T2 - a review
AU - Vaishnani, Mira J.
AU - Bijani, Sabera
AU - Rahamathulla, Mohamed
AU - Baldaniya, Lalji
AU - Jain, Vicky
AU - Thajudeen, Kamal Y.
AU - Ahmed, Mohammed Muqtader
AU - Farhana, Syeda Ayesha
AU - Pasha, Ismail
N1 - Publisher Copyright:
© 2024 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.
PY - 2024
Y1 - 2024
N2 - 1,2,3-triazole is a five-member nitrogen-containing heterocyclic compound with diverse biological activities. A number of 1,2,3-triazole-containing FDA-approved drugs are available on the market, and many other pharmaceutically significant potential molecules are under clinical investigation. Therefore, it is fairly reasonable to anticipate that there will be an increase in demand for new triazole-containing drugs in the coming future. Because of its broad pharmacological applications, it has recently attracted the attention of scientists worldwide. This review provides a concise summary of the synthetic techniques for triazole compounds from various strategies and their medical importance as a lead structure for the enhancement of therapeutic molecules.
AB - 1,2,3-triazole is a five-member nitrogen-containing heterocyclic compound with diverse biological activities. A number of 1,2,3-triazole-containing FDA-approved drugs are available on the market, and many other pharmaceutically significant potential molecules are under clinical investigation. Therefore, it is fairly reasonable to anticipate that there will be an increase in demand for new triazole-containing drugs in the coming future. Because of its broad pharmacological applications, it has recently attracted the attention of scientists worldwide. This review provides a concise summary of the synthetic techniques for triazole compounds from various strategies and their medical importance as a lead structure for the enhancement of therapeutic molecules.
KW - 1,2,3triazole
KW - Huisgen azide–alkyne cycloaddition
KW - azide-alkynes cycloaddition
KW - biological importance
KW - click chemistry
UR - https://www.scopus.com/pages/publications/85183936451
U2 - 10.1080/17518253.2024.2307989
DO - 10.1080/17518253.2024.2307989
M3 - Review article
AN - SCOPUS:85183936451
SN - 1751-8253
VL - 17
JO - Green Chemistry Letters and Reviews
JF - Green Chemistry Letters and Reviews
IS - 1
M1 - 2307989
ER -