Results 211 to 220 of about 48,200 (259)
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On Triazoles. VI. The acylation of 5‐amino‐1,2,4‐triazoles
Journal of Heterocyclic Chemistry, 1987AbstractThe isomeric and tautomeric structure of I and II type monoacylated 5‐amino‐1,2,4‐triazole derivatives was studied with the help of their ir, uv, pmr and cmr spectra as well as model compounds prepared for this purpose. It was stated that the structure of the I type ring‐acylated derivatives is 2o and those of their II type isomers is 5a.
József Reiter +2 more
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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 ...
A.D.M. Curtis, N. Jennings
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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 ...
A.D.M. Curtis, N. Jennings
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Journal of Molecular Modeling
Theoretical studies of a series of heterocyclic high energetic molecules, triazole-benzene, and triazole-pyridine derivatives were conducted using density functional theory (DFT) at the B3PW91 6-31G(d,p)levels. Detonation properties, detonation velocity, and detonation pressure are evaluated using Kamlet-Jacobs equation.
Alan M, Johnson, Kannan, V, Nisha, K
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Theoretical studies of a series of heterocyclic high energetic molecules, triazole-benzene, and triazole-pyridine derivatives were conducted using density functional theory (DFT) at the B3PW91 6-31G(d,p)levels. Detonation properties, detonation velocity, and detonation pressure are evaluated using Kamlet-Jacobs equation.
Alan M, Johnson, Kannan, V, Nisha, K
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The Chemistry of the Vicinal Triazoles.
Chemical Reviews, 1950F R, BENSON, W L, SAVELL
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Ring-Opening Coupling of Cyclopropanol with 1,2,3-Triazole for the Synthesis of Fused Triazoles
Organic LettersA radical ring-opening arylation of cyclopropanol with 1,2,3-triazole has been achieved. This synthetic protocol provides straightforward access to a wide range of structurally diverse and chiral 4,5,6,7-tetrahydro[1,2,3]triazolo[1,5-a]pyridines with high efficiency from readily available chiral cyclopropanols.
Yi Wu +8 more
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