Results 291 to 300 of about 103,024 (350)
Some of the next articles are maybe not open access.
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
openaire +1 more source
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
openaire +1 more source
Triazoles. Part VIII. 1,2,4-Triazole-3-sulphonic acids
Journal of the Chemical Society C: Organic, 1967Free 1,2,4-triazole-3-sulphonic acids have been prepared by oxidation of the corresponding thiols with potassium permanganate or, preferably, by treatment of sulphonyl chlorides with ethanol.
A. J. Blackman +2 more
openaire +1 more source
Mass spectra of 1,2,4‐triazoles—II: Alkyl 1,2,4‐triazoles
Organic Mass Spectrometry, 1973AbstractThe mass spectra of monomethyl 1,2,4‐triazoles contain fragment ions produced by specific cleavage of the heterocyclic ring. A major fragmentation from many molecular ions involves the elimination of HCN, but loss of N2 is either very small or completely absent.
A. J. Blackman, J. H. Bowie
openaire +1 more source
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
openaire +1 more source
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
openaire +1 more source
Fragmentation de Triazoles Sous L'Impact Electronique—II 1,2,3‐Triazole
Organic Mass Spectrometry, 1973AbstractLa similitude de comportement des 1,2,4‐ et 1,2,3‐triazoles sous l'impact électronique est attribuée à la formation de structures ioniques communes. L'étude des transitions métastables correspondant à al perte d'une molécule d'azote semble indiquer que, dans le cas du 1,2,3‐triazole, les deux formes tautoméres coexistent à l'état gzaeux et qu ...
A. Maquestiau +3 more
openaire +1 more source
ChemInform Abstract: 1,2,4‐TRIAZOLES. VII. METHYLATION OF 1,2,4‐TRIAZOLES
Chemischer Informationsdienst, 1977AbstractMethylierung von 1,2,4‐Triazol und dessen symmetrisch 3,5‐disubst.
M. UDA, Y. HISAZUMI, K. SATO, S. KUBOTA
openaire +1 more source
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.
G. I. Tsypin +3 more
openaire +1 more source
A review on ‘triazoles’: their chemistry, synthesis and pharmacological potentials
Journal of the Iranian Chemical Society, 2021Deepali Dixit, P. Verma, R. K. Marwaha
semanticscholar +1 more source

