Journal ArticleDOI
Molecular rearrangements of 4-iminomethyl-1,2,3-triazoles. Replacement of 1-aryl substituents in 1H-1,2,3-triazole-4-carbaldehydes
Reads0
Chats0
TLDR
In this article, the two structural isomers, 4 and 5, of 1-substituted-4-iminomethyl-1,2,3-triazoles are interconvertible when heated in dimethyl sulfoxide at 80°.About:
This article is published in Journal of Heterocyclic Chemistry.The article was published on 1990-11-01. It has received 38 citations till now. The article focuses on the topics: Nitrile & 1,2,3-Triazole.read more
Citations
More filters
Journal ArticleDOI
1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring
TL;DR: In this paper, the synthetic routes to substituted 1,2,3-triazoles, including those containing functional groups, based on cyclisation of various nitrogen compounds published during the last 15 years are described.
Journal ArticleDOI
Synthesis and investigation of tuberculosis inhibition activities of some 1,2,3-triazole derivatives.
TL;DR: In this study, alpha-diazo-beta-oxoaldehyde compounds were condensed with different amines to yield 4-acyl-1H-1,2,3-triazole derivatives, which were investigated for their inhibition activities against tuberculosis.
Journal ArticleDOI
Synthesis of novel 1,2,3-triazole substituted-N-alkyl/aryl nitrone derivatives, their anti-inflammatory and anticancer activity
P. Sambasiva Rao,C. Kurumurthy,B. Veeraswamy,G. Santhosh Kumar,Yedla Poornachandra,C. Ganesh Kumar,Sathish Babu Vasamsetti,Srigiridhar Kotamraju,Banda Narsaiah +8 more
TL;DR: A series of novel 1,2,3-triazole substituted N-phenyl nitrone derivatives 5a-e and 6a-p exhibited significant inhibition of IL-1β secretion as a measure of anti-inflammatory activity against various cancer cell lines.
Journal ArticleDOI
Regioselective synthesis of 1,2,3-triazole derivatives via 1,3-dipolar cycloaddition reactions in water.
Zhong-Xia Wang,Hua-Li Qin +1 more
TL;DR: In this paper, arylacetylene with an azide in hot water gave 1,4-disubstituted 1,2,3-triazoles in high yields, while similar reaction between a terminal aliphatic alkyne and an azides (except m-nitroazidobenzene) afforded a mixture of regioisomers with the ratio of 1, 4 to 1,5-isomers ranging from 3 : 1 to 28.6 : 1.
References
More filters
Journal ArticleDOI
Ueber intramolekulare Umlagerungen. Umlagerungen in der Reihe des 1, 2, 3‐Triazols
Journal ArticleDOI
Molecular rearrangements of five-membered ring heteromonocycles
TL;DR: In this article, the authors classified molecular rearrangements of five-membered ring heterocycles into five categories based on the number of participating side-chain atoms: Dimroth rearrangement, Dimroth contraction-ring expansion (DRCE), Dimroth expansion, Cornforth, Boulton-Katritzky, and bond-switch rearranging.