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2-Butyl-5-chloro-3H-imidazole-4-carbaldehyde as a new synthon for the synthesis of fused ring heterocycles via intramolecular 1,3-dipolar cycloaddition reactions

✍ Scribed by S. L. Gaonkar; K. M. Lokanatha Rai


Publisher
Journal of Heterocyclic Chemistry
Year
2010
Tongue
English
Weight
81 KB
Volume
47
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

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The title compound 2‐butyl‐5‐chloro‐3__H__‐imidazole‐4‐carbaldehyde was transformed into tricyclic heterocycles by substituting the chlorine atom by an unsaturated thiolate or alkoxide and then converting aldehyde function into 1,3‐dipole. Chloramine‐T was used as an efficient reagent for the generation of 1,3‐dipoles, which resulted the formation of fused ring heterocycles via intramolecular 1,3‐dipolar cycloaddition reaction. The method is very useful for the construction of many biologically active fused heterocycles. J. Heterocyclic Chem., (2010).


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