Gaonkar, Santosh L. and Rai, K. M. Lokanatha (2010) 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. Journal of Heterocyclic Chemistry, 47 (3). pp. 543-546. ISSN 1943-5193
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Abstract The title compound 2-butyl-5-chloro-3H-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).
| Item Type: | Article |
|---|---|
| Subjects: | C Chemical Science > Chemistry |
| Divisions: | Department of > Chemistry |
| Depositing User: | LA manjunath user |
| Date Deposited: | 12 Jul 2019 10:25 |
| Last Modified: | 19 Jan 2023 06:02 |
| URI: | http://eprints.uni-mysore.ac.in/id/eprint/5152 |
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