an environmentally benign and clean synthesis of aryl-hydrazones by reacting variety of carbonyl compounds with thiosemicarbazide, semicarbazide, aminoguanidine, and phenyl hydrazine has been achieved using aqueous extract of acacia concinna pods as a natural surfactant type catalyst. we found that the aqueous extract of acacia concinna pods could be effectively used for the synthesis of aryl-h...

A series of benzaldehyde substituted phenyl carbonyl hydrazones has been synthesized and their formylation has been carried out by using Vilsmeier-Haack reaction. All the hydrazones and their formyl derivatives were screened for antibacterial activity.

Aldehyde phenyl hydrazones 2a-i undergo oxidative dehydrogenation with Chloramine-T to give nitrile imines, which are trapped in situ by ethyl oleate 1 to afford 8-(5-Aryl-4-octyl-2-phenyl-3,4-dihydro-2Hpyrazol-3-yl)-octanoic acid ethyl esters 3a-i in good yield. The structures of the cycloadducts were confirmed by spectral studies and elemental analysis.

An environmentally benign and clean synthesis of aryl-hydrazones by reacting variety of carbonyl compounds with thiosemicarbazide, semicarbazide, aminoguanidine, and phenyl hydrazine has been achieved using aqueous extract of Acacia concinna pods as a natural surfactant type catalyst. We found that the aqueous extract of Acacia concinna pods could be effectively used for the synthesis of aryl-h...

In the present work a new series of 3-alkyl-2,6-diarylpiperidin-4-one-2-thienoyl hydrazones have synthesized by the reaction of 3-alkyl-2, 6-diarylpiperidin-4-one with 2-thiophenecarboxylic acid hydrazide and characterized by spectral (IR, H NMR, C NMR, HSQC, HMBC, NOESY and COSY) techniques. The hydrazones were screened for their in vitro antibacterial and antifungal activities against some se...

Some new 3-acetyl-5-(3-chloro-1-benzo[b]thiophen-2-yl)-2-substituted phenyl-2,3-dihydro-1,3,4-oxadiazoles and 2-(3-chloro-1-benzo[b]thiophen-2-yl)-5-substituted phenyl-1,3,4-oxadiazoles have been synthesized and evaluated for antimicrobial activity. Initially, 3-chloro-1-benzo[b]thiophene-2-carbonyl chloride (1) was prepared from cinnamic acid in the presence of chlorobenzene and thionyl chlori...

A strategy involving palladium-catalyzed cyclization of halo-phenyl hydrazones and aryl isocyanates provides a convenient approach to the synthesis of 1,3,4-benzotriazepines (4) or 1-arylamide-1H-indazoles (5) in good isolated yields. Microwave irradiation was found to afford high reaction efficiency, while the choice of halophenyl hydrazone had an effect on the pathway of the reaction.

In the title complex, [Sn(2)(C(7)H(7))(4)(C(10)H(8)N(2)O(3))(2)(C(2)H(5)OH)(2)], the Sn(IV) atom is seven-coordinated in a distorted penta-gonal-bipyramidal geometry by three O atoms and one N atom from the pyruvate benzoyl hydrazone ligand, one ethanol O atom and two axial C atoms from trans-benzyl groups, thus forming a dimeric mol-ecule ([Formula: see text] symmetry) via weak Sn-O inter-acti...

The title compound, C(23)H(20)N(4)O, is a heterocyclic phenyl-hydrazone Schiff base with a pyrazole moiety. In the crystal, a variety of inter-actions occur, including N-H⋯π and π-π stacking between the phenyl ring of the phenyl-hydrazinyl group and its symmetry-generated equivalent [centroid-centroid distance = 3.6512 (7) Å].

The title compound, C(14)H(11)BrN(4)O(4), contains 3-bromo-phenyl and 2,4-dinitro-phenyl groups on opposite sides of a hydrazone unit and crystallizes with two mol-ecules in the asymmetric unit. The dihedral angles between the two ring systems in each mol-ecule are 2.0 (1) and 2.5 (4)°. Weak C-H⋯O hydrogen bonds and weak π-π stacking inter-actions [centroid-centroid distance = 3.7269 (14) Å] he...