Search results for "3-triazole"
showing 10 items of 42 documents
CCDC 766326: Experimental Crystal Structure Determination
2010
Related Article: L.Kiss, E.Forro, R.Sillanpaa, F.Fulop|2010|Tetrahedron|66|3599|doi:10.1016/j.tet.2010.03.030
CCDC 704876: Experimental Crystal Structure Determination
2009
Related Article: L.Kiss, E.Forro, R.Sillanpaa, F.Fulop|2008|Tetrahedron:Asymm.|19|2856|doi:10.1016/j.tetasy.2008.11.035
CCDC 806636: Experimental Crystal Structure Determination
2011
Related Article: S.Zeghada, G.Bentabed-Ababsa, A.Derdour, S.Abdelmounim, L.R.Domingo, J.A.Saez, T.Roisnel, E.Nassar, F.Mongin|2011|Org.Biomol.Chem.|9|4295|doi:10.1039/c1ob05176h
CCDC 2005159: Experimental Crystal Structure Determination
2021
Related Article: Argha Saha, Srimanta Guin, Wajid Ali, Trisha Bhattacharya, Sheuli Sasmal, Nupur Goswami, Gaurav Prakash, Soumya Kumar Sinha, Hediyala B. Chandrashekar, S. S. Anjana, Debabrata Maiti|2021|Cell Press: Chem|7|948|doi:10.1016/j.chempr.2021.01.003
CCDC 2005161: Experimental Crystal Structure Determination
2021
Related Article: Argha Saha, Srimanta Guin, Wajid Ali, Trisha Bhattacharya, Sheuli Sasmal, Nupur Goswami, Gaurav Prakash, Soumya Kumar Sinha, Hediyala B. Chandrashekar, S. S. Anjana, Debabrata Maiti|2021|Cell Press: Chem|7|948|doi:10.1016/j.chempr.2021.01.003
CCDC 2049729: Experimental Crystal Structure Determination
2021
Related Article: Philipp Dierks, Ayla Kruse, Olga S. Bokareva, Mohammed J. Al-Marri, Jens Kalmbach, Marc Baltrun, Adam Neuba, Roland Schoch, Stephan Hohloch, Katja Heinze, Michael Seitz, Oliver Kühn, Stefan Lochbrunner, Matthias Bauer|2021|Chem.Commun.|57|6640|doi:10.1039/D1CC01716K
Synthesis of conformationally restricted 1,2,3-triazole-substituted ethyl β- and γ-aminocyclopentanecarboxylate stereoisomers. Multifunctionalized al…
2010
Abstract Stereoisomers of 1,2,3-triazole-functionalized, conformationally restricted β- or γ-amino esters with a cyclopentane skeleton were efficiently synthetized from the bicyclic β-lactam 6-azabicyclo[3.2.0]hept-3-en-7-one (1) and Vince γ-lactam (15) in five or six steps involving the azide–alkyne 1,3-dipolar cycloaddition of azido-substituted amino ester stereoisomers with nonsymmetric acetylenes. The azide–alkyne click reactions were investigated under thermal and Cu(I)-catalyzed conditions. Surprisingly, the thermally induced cycloaddition furnished the corresponding 1,4-triazoles regioselectively, which also took place selectively in response to Cu(I) catalysis.
ChemInform Abstract: 1,2,3-Triazole in Heterocyclic Compounds, Endowed with Biological Activity, Through 1,3-Dipolar Cycloadditions
2014
1,3-Dipolar cycloaddition reactions can be considered a powerful synthetic tool in the building of heterocyclic rings, with applications in different fields. In this review we focus on the synthesis of biologically active compounds possessing the 1,2,3-triazole core through 1,3-dipolar cycloaddition reactions. The 1,2,3-triazole skeleton can be present as a single disubstituted ring, as a linker between two molecules, or embedded in a polyheterocycle. The cycloaddition reactions are usually catalysed by copper or ruthenium. Domino reactions can be achieved through dipolarophile anion formation, generally followed by cyclisation. The variety of attainable heterocyclic structures gives an ill…
Systematic investigation of the adsorption and inhibition properties of a new clickable 1,2,3‐triazole compound for mild steel in 1 M HCl medium
2021
An Overview on the Performance of 1,2,3-Triazole Derivatives as Corrosion Inhibitors for Metal Surfaces
2021
This review accounts for the most recent and significant research results from the literature on the design and synthesis of 1,2,3-triazole compounds and their usefulness as molecular well-defined corrosion inhibitors for steels, copper, iron, aluminum, and their alloys in several aggressive media. Of particular interest are the 1,4-disubstituted 1,2,3-triazole derivatives prepared in a regioselective manner under copper-catalyzed azide-alkyne cycloaddition (CuAAC) click reactions. They are easily and straightforwardly prepared compounds, non-toxic, environmentally friendly, and stable products to the hydrolysis under acidic conditions. Moreover, they have shown a good efficiency as corrosi…