Results 21 to 30 of about 94,532 (279)

Recent Progress in Catalytic Synthesis of 1,2,3-Triazoles

open access: yesCatalysts, 2021
1,2,3-triazoles represent a functional heterocyclic core that has been at the center of modern organic chemistry since the beginning of click chemistry. Being a versatile framework, such an aromatic ring can be observed in uncountable molecules useful in
A. De Nino   +6 more
semanticscholar   +1 more source

Three-component synthesis of 1,2,3-triazoles in the presence of PVC-supported triazole-copper complex by click reaction [PDF]

open access: yesشیمی کاربردی روز, 2020
In this research work novel PVC-supported triazole-copper(I) iodide catalyst (PVC–Triazole–CuI) was prepared and used the for synthesis of 1,2,3-triazoles.
Ali Keivanloo   +2 more
doaj   +1 more source

Versatile Synthetic Platform for 1,2,3-Triazole Chemistry

open access: yesACS Omega, 2022
1,2,3-Triazole scaffolds are not obtained in nature, but they are still intensely investigated by synthetic chemists in various fields due to their excellent properties and green synthetic routes. This review will provide a library of all synthetic routes used in the past 21 years to synthesize 1,2,3-triazoles and their derivatives using various metal ...
Disha P. Vala   +2 more
openaire   +3 more sources

5-Formyltriazoles as Valuable Starting Materials for Unsymmetrically Substituted Bi-1,2,3-Triazoles

open access: yesFrontiers in Chemistry, 2020
Herein, we present the first synthetic methodologies toward non-symmetrical 5,5′-C, C-linked bi-1,2,3-triazoles starting from 5-formyl-1,2,3-triazole via two related pathways.
Robby Vroemans   +3 more
doaj   +1 more source

Enzymatic Macrocyclization of 1,2,3‐Triazole Peptide Mimetics [PDF]

open access: yesAngewandte Chemie International Edition, 2016
AbstractThe macrocyclization of linear peptides is very often accompanied by significant improvements in their stability and biological activity. Many strategies are available for their chemical macrocyclization, however, enzyme‐mediated methods remain of great interest in terms of synthetic utility.
Emilia Oueis   +3 more
openaire   +7 more sources

Synthesis of β-triazolylenones via metal-free desulfonylative alkylation of N-tosyl-1,2,3-triazoles

open access: yesBeilstein Journal of Organic Chemistry, 2021
Desulfonylative alkylation of N-tosyl-1,2,3-triazoles under metal-free conditions leading to β-triazolylenones is reported here. The present study encompasses the synthesis of triazoles with a new substitution pattern in a single step from cyclic 1,3 ...
Soumyaranjan Pati   +3 more
doaj   +1 more source

Synthesis of Deuterated 1,2,3-Triazoles [PDF]

open access: yesThe Journal of Organic Chemistry, 2012
The copper-catalyzed azide-alkyne cycloaddition (CuAAC) is a highly effective method for the selective incorporation of deuterium atom into the C-5 position of the 1,2,3-triazole structure. Reactions of alkynes and azides can be conveniently carried out in a biphasic medium of CH(2)Cl(2)/D(2)O, using the CuSO(4)/Na ascorbate system. The mildness of the
Hari K. Akula, Mahesh K. Lakshman
openaire   +3 more sources

Study of the mechanism of antibacterial action of 1,4-di- and 1,4,5-trisubstituted 1Н-1,2,3-triazoles by molecular modeling

open access: yesЖурнал Белорусского государственного университета: Химия, 2020
The target for antibacterial action of 1,4-di- and 1,4,5-trisubstituted 1H-1,2,3-triazoles against E. coli ATCC 25922 and S. aureus ATCC 6538 was proposed.
Cyril M. Verbilo   +4 more
doaj   +1 more source

Triazoles and Their Derivatives: Chemistry, Synthesis, and Therapeutic Applications

open access: yesFrontiers in Molecular Biosciences, 2022
Among the nitrogen-containing heterocyclic compounds, triazoles emerge with superior pharmacological applications. Structurally, there are two types of five-membered triazoles: 1,2,3-triazole and 1,2,4-triazole.
Mohammed M. Matin   +8 more
doaj   +1 more source

1,5-Disubstituted 1,2,3-Triazoles as Amide Bond Isosteres Yield Novel Tumor-Targeting Minigastrin Analogs.

open access: yesACS Medicinal Chemistry Letters, 2021
1,5-Disubstituted 1,2,3-triazoles (1,5-Tz) are considered bioisosteres of cis-amide bonds. However, their use for enhancing the pharmacological properties of peptides or proteins is not yet well established.
N. Grob   +4 more
semanticscholar   +1 more source

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