Results 351 to 360 of about 178,442 (380)
Some of the next articles are maybe not open access.
2006
[288-88-0] C2H3N3 (MW 69.08) InChI = 1S/C2H3N3/c1-3-2-5-4-1/h1-2H,(H,3,4,5) InChIKey = NSPMIYGKQJPBQR-UHFFFAOYSA-N (transacylating agent used for ester and amide synthesis, especially in peptide synthesis; cyclization reactions; oligonucleotide synthesis) Physical Data: mp 120–121 °C; bp 260 °C (dec above 187 °C); fp 140
Christopher S. Siedem +1 more
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[288-88-0] C2H3N3 (MW 69.08) InChI = 1S/C2H3N3/c1-3-2-5-4-1/h1-2H,(H,3,4,5) InChIKey = NSPMIYGKQJPBQR-UHFFFAOYSA-N (transacylating agent used for ester and amide synthesis, especially in peptide synthesis; cyclization reactions; oligonucleotide synthesis) Physical Data: mp 120–121 °C; bp 260 °C (dec above 187 °C); fp 140
Christopher S. Siedem +1 more
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The Thermochemistry and Initial Decomposition Pathways of Triazole Energetic Materials.
Journal of Physical Chemistry A, 2020A thorough investigation on the initial decomposition pathways of triazoles and their nitro-substituted derivatives has been conducted using MP2 method for optimization and DLPNO-CCSD(T) method for energy.
Meiheng Lu +5 more
semanticscholar +1 more source
1974
Publisher Summary This chapter focuses on the chemistry of monocyclic1,2,3-triazoles as much of the chemistry of benzotriazoles and other fused systems has little in common with monocyclic triazole chemistry and provides a broad survey of methods of synthesis and reactions of triazoles. There has been considerable interest in 1,2,3-triazoles as light
T.L. Gilchrist, G.E. Gymer
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Publisher Summary This chapter focuses on the chemistry of monocyclic1,2,3-triazoles as much of the chemistry of benzotriazoles and other fused systems has little in common with monocyclic triazole chemistry and provides a broad survey of methods of synthesis and reactions of triazoles. There has been considerable interest in 1,2,3-triazoles as light
T.L. Gilchrist, G.E. Gymer
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A Recent Portrait of Bioactive Triazoles
Current Bioactive Compounds, 2010Scientists have extensively explored new synthetic routes in order to obtain 1,2,3- and 1,2,4-triazoles as they represent a very interesting class of compounds due to their wide range of biological activities such as antitumor, antiinflammatory, analgesic, antifungal, antibacterial, antiviral, etc.
PIBIRI, Ivana, BUSCEMI, Silvestre
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QSAR Prediction of Aquatic Toxicity of Triazoles and Benzo-Triazoles
2011Triazoles and benzo-triazoles (TAZ/BTAZ) are potentially hazardous chemicals that adversely affect humans and other non-target species, and are on the list of substances of very high concern (SVHC) in the European regulation of chemicals REACH. TAZ/BTAZ are synthetic molecules used in various industrial processes (to obtain pharmaceuticals and ...
CASSANI, STEFANO +5 more
openaire +3 more sources
2008
This chapter provides a critical update on developments in the chemistry of 1,2,4-triazoles over the last decade. 1,2,4-Triazoles have remained the topic of much research, primarily due to their ubiquitous presence in many pharmaceutical agents and, more recently, in other functional materials with uses in engineering as corrosion inhibitors and in ...
N. Jennings, Anthony D.M. Curtis
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This chapter provides a critical update on developments in the chemistry of 1,2,4-triazoles over the last decade. 1,2,4-Triazoles have remained the topic of much research, primarily due to their ubiquitous presence in many pharmaceutical agents and, more recently, in other functional materials with uses in engineering as corrosion inhibitors and in ...
N. Jennings, Anthony D.M. Curtis
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Tetrahedron Letters, 1969
Photolytic cleavage of vic-triazole ring when unsubstituted at N, finding phenylacetonitrile production ...
R. Selvarajan, J.H. Boyer
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Photolytic cleavage of vic-triazole ring when unsubstituted at N, finding phenylacetonitrile production ...
R. Selvarajan, J.H. Boyer
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Synthesis of a 16-Triazole Phorboxazole A Analog via Intramolecular Triazole Formation
HETEROCYCLES, 2007AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Lu Ying, Craig J. Forsyth
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Synthesis of 1-(1,2,4-triazol-3-yl)-1,2,3-triazoles
Chemistry of Heterocyclic Compounds, 19801-(1,2,4-Triazol-3-yl)-1,2,3-triazoles were obtained by 1,3-dipolar cycloaddition of 3-azido-1,2,4-triazole to acetylene derivatives.
T. F. Sharamet +3 more
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