Synthetic strategies and significance of pyrroline analogs

Ajay Kumar, K. and Lokeshwari, D. M. and Chandramouly, M. and Vasanth Kumar, G. (2013) Synthetic strategies and significance of pyrroline analogs. Research Journal of Pharmacy and Technology, 6 (2). pp. 137-142. ISSN 0974-3618

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The isomeric forms of pyrrolines; 1-pyrroline, 2-pyrroline and 3-pyrroline and their derivatives are an important class of heterocyclic compounds. They exhibit wide range of biological applications, particularly in their versatile enzymatic activity. This brief review article presents up to date information about the strategies adopted for the synthesis of pyrrolines and their derivatives. Also describes the biological activities associated with them, more emphasis was given on their enzymatic activity and impact of these molecules on diseases in plants and animals.

Item Type: Article
Uncontrolled Keywords: 2 acetyl 1 pyrroline, 3 pyrroline, 5, 5 diethoxyphosphoryl 5 methyl 1 pyrroline 1 oxide, 5 dimethyl 4 phenyl 2 (3-pyridyl) 1 pyrroline, abiotic stress, amination, amino acid sequence, annulation reaction, aqueous solution, AtP5CS gene, aziridine derivative, bioaccumulation, biological activity, biotransformation, carboxylic acid, catalysis, chemical analysis, chemical interaction, chemical structure, Cope rearrangement, cyanation, cyclization, cycloaddition, drought tolerance, enzyme activity, gene, heart muscle ischemia, human, hydrogenation, hyperprolinemia, Mannich reaction, Michael addition, nonhuman, oxidoreductase, proline, pyrroline 5 carboxylate synthase, pyrroline 5 carboxylic acid, pyrroline 5 carboxylic acid dehydrogenase, pyrroline derivative, reduction kinetics, reperfusion injury, review, ring closing metathesis, silver nitrate, solvent effect, spin trapping, substitution reaction, synthesis, synthetase, tosylchloramide sodium, unclassified drug
Subjects: C Chemical Science > Chemistry
Divisions: Yuvaraj college > Chemistry
Depositing User: Arshiya Kousar
Date Deposited: 15 Oct 2019 05:35
Last Modified: 15 Oct 2019 05:35

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