2015
DOI: 10.18052/www.scipress.com/ilcpa.57.126
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Malononitrile: A Versatile Active Methylene Group

Abstract: Abstract:The title role of malononitrile in the development of Knoevenagel condensation of organic synthesis and their new findings are explored in this review. The active methylene group of malononitriles is very important attacking part in the heterocyclic conversions and also having a great potency towards several microbial and biological systems. Contents:

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Cited by 7 publications
(7 citation statements)
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“…The afforded cyclic imide treated with various substituted aromatic aldehyde furnished a series of bis-chalcones. A series of bis isoxazole were prepared in good yield by cyclization of bis chalcone with hydroxyl amine hydrochloride in presence neutral alumina under solvent Journal of Advanced Scientific Research, 2022; 13 (5): June-2022 free microwave irradiation. The afforded bis isoxazole were confirmed by IR, 1 H NMR and elemental analysis.…”
Section: Chemistrymentioning
confidence: 99%
See 2 more Smart Citations
“…The afforded cyclic imide treated with various substituted aromatic aldehyde furnished a series of bis-chalcones. A series of bis isoxazole were prepared in good yield by cyclization of bis chalcone with hydroxyl amine hydrochloride in presence neutral alumina under solvent Journal of Advanced Scientific Research, 2022; 13 (5): June-2022 free microwave irradiation. The afforded bis isoxazole were confirmed by IR, 1 H NMR and elemental analysis.…”
Section: Chemistrymentioning
confidence: 99%
“…A series of bis isoxazole were prepared in good yield by cyclization of bis chalcone with hydroxyl amine hydrochloride in presence neutral alumina under solvent Journal of Advanced Scientific Research, 2022; 13 (5): June-2022 free microwave irradiation. The afforded bis isoxazole were confirmed by IR, 1 H NMR and elemental analysis. , δ ppm): 6.38-8.12 (m, 7H, Ar-H and =C-H), 2.53 (S, 3H, -CH 3 ).…”
Section: Chemistrymentioning
confidence: 99%
See 1 more Smart Citation
“…2,35,36 This type of imides, also have a variety of biological and pharmaceutical uses such as CNS depressant, analgesic, antitumor, cytostatic, anorexigenic, nerve conduction blocking, antispasmodic, bacteriostatic, muscle relaxant, hypotensive, antibacterial, antifungal and antitubercular. 2,37,38 Chiral succinimides with antifungal activity have shown higher activity than the corresponding racemic mixtures, thus opening new avenues for the development of highly active drugs containing 3-and 3,4-substituted chiral succinimides. Glutarimide derivatives (4) have a hydrophobic nature, which accounts for their antibacterial and antifungal potencies.…”
Section: Figurementioning
confidence: 99%
“…Glutarimide derivatives (4) have a hydrophobic nature, which accounts for their antibacterial and antifungal potencies. 2,40 The antitumoral and analgesic effects, as well as the effect on the CNS have been reported. 2 The glutarimide moiety is present in alkaloids, such as filantimide, julocrotine and streptimidone, among others.…”
Section: Figurementioning
confidence: 99%