Replacement of aryl by alkyl in 1-substituted 1H-1,2,3-triazole-4-carbaldehydes
- 1 January 1990
- journal article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 5,p. 1492-1493
- https://doi.org/10.1039/p19900001492
Abstract
1-Phenyl-1,2,3-triazole-4-carbaldehyde is readily transformed into 1 -alkyl-1,2,3-triazole-4-carbalde-hydes by thermal isomerization of the corresponding imines, followed by acid hydrolysis.Keywords
This publication has 12 references indexed in Scilit:
- Ring‐degenerate rearrangement of 5‐amino‐4‐iminomethyl‐1, 2, 3‐triazolesJournal of Heterocyclic Chemistry, 1989
- Synthesis of 1‐Amino‐5‐(Substituted)Amino‐1,2,3‐TriazolesBulletin des Sociétés Chimiques Belges, 1989
- Influence of electron-withdrawing N-1 substituents on the thermal behaviour of 5-azido-1,2,3-triazolesTetrahedron, 1989
- Thermal Rearrangement of 1-Substituted 5-Azido-4-Cyano-1H-1,2,3-TriazolesBulletin des Sociétés Chimiques Belges, 1989
- Synthesis and thermal rearrangement of 5-diazomethyl-1,2,3-triazolesTetrahedron, 1988
- Synthesis and thermolysis of 4-substituted 5-azido-l-phenyl-l,2,3-triazolesTetrahedron, 1988
- Molecular rearrangements of 5-azido substituted 1,2,3-triazolesTetrahedron, 1985
- Heterocyclic studies. 2. 5‐Chloro‐1H‐1,2,3‐triazole‐4‐carboxaldehydes, preparation and rearrangement reactionsJournal of Heterocyclic Chemistry, 1984
- Molecular rearrangements of five‐membered ring heteromonocyclesJournal of Heterocyclic Chemistry, 1984
- 1,2,3-Triazoles and their Benzo DerivativesPublished by Elsevier ,1984