Results 161 to 170 of about 8,430 (199)

Structural basis of the impact sensitivities of 1-picryl-1,2,3-triazole, 2-picryl-1,2,3-triazole, 4-nitro-1-picryl-1,2,3-triazole, and 4-nitro-2-picryl-1,2,3-triazole

The Journal of Physical Chemistry, 1989
The isomeric pairs 1-picryl-1,2,3-triazole, 2-picryl-1,2,3-triazole and 4-nitro-1-picryl-1,2,3-triazole, 4-nitro-1-picryl-1,2,3-triazole differ dramatically in their impact sensitivity. Since these pairs of compounds have identical oxygen balance this strongly suggests that there is a difference in the decomposition mechanism.
C. B. Storm, R. R. Ryan, J. P. Ritchie, J. H. Hall, S. M. Bachrach   +4 more
openaire   +1 more source

A vibrational assignment for 1,2,3-triazole

Journal of the Chemical Society B: Physical Organic, 1969
I.r. spectra of 1,2,3-triazole in the vapour and liquid states and in solution are reported and discussed. From these, and by comparison with the spectra of other simple five-membered heterocycles, vibrational assignments are proposed. The i.r. spectra is satisfactorily interpreted in terms of an asymmetric structure.
E. Borello, A. Zecchina, E. Guglielminotti   +2 more
openaire   +1 more source

Mass spectra of 1,2,3-triazoles

Journal of the Chemical Society, Perkin Transactions 1, 1979
The mass spectra of substituted 1,2,3-triazoles [RTR′, (1)](R′= H, CO2X, COR″, pyrazolyl, or isoxazolyl) are discussed. For a wide variety of structural types, P+ is always strong and [P+ 1]+ is often of significant intensity. Subsequent breakdown patterns are strongly dependent on the substituents R and R′.
Sidney I. Miller, Ruey-Rong Lii, Yoshinari Tanaka   +2 more
openaire   +1 more source

1,2,3‐Triazoles in Peptidomimetic Chemistry

European Journal of Organic Chemistry, 2011
AbstractThe ability to synthesise small peptidomimetics that mimic the secondary structure of proteins is an ever expanding area of research directed at sourcing new medicinal agents and biological probes. A significant current challenge is to mimic protein epitopes under physiological conditions using small peptidomimetics that are easy to prepare ...
Pedersen, D., Abell, A.
openaire   +2 more sources

1,2,3-Triazoles

2022
Nuno M.M. Moura, Augusto C. Tomé
openaire   +1 more source

Pharmacological Significance of 1,2,3-Triazoles

Click chemistry is not a single specific reaction, but was meant to mimic nature, which also generates substances by joining small modular units. The 1,3-dipolar azide, alkyne cycloaddition (CuAAC) reaction catalyzed by copper, as nearly quantitative and easy to execute has emerged as the leading example of “click chemistry”.
Mubarak Hanif Shaikh, Amol A. Nagargoje, Dattatraya N. Pansare, Bapurao B. Shingate   +3 more
openaire   +1 more source

1,2,3-Triazoles

1996
Wei-Qiang Fan, Alan R. Katritzky
openaire   +1 more source

Influence of Phosphorus Doping on Triazole-Based g-C3N5 Nanosheets for Enhanced Photoelectrochemical and Photocatalytic Performance

ACS Applied Materials & Interfaces, 2021
Chechia Hu, Masaaki Yoshida
exaly  

Catalysis by 1,2,3-triazole- and related transition-metal complexes

Coordination Chemistry Reviews, 2014
Didier Astruc, Pengxiang Zhao
exaly  

Pharmacological significance of triazole scaffold

Journal of Enzyme Inhibition and Medicinal Chemistry, 2011
Prabodh Chander Sharma, Rajeev Kharb
exaly