77203-49-7Relevant academic research and scientific papers
L-Proline as an efficient catalyst for synthesis of aldimines at ambient temperature condition
Kottawar,Goswami,Thorat,Bhusare
experimental part, p. 1859 - 1863 (2012/06/01)
Some new aldimines were synthesized from substituted 2-amino thiazoles and different aromatic aldehydes using L-proline as an efficient catalyst. The structure elucidation of aldimines has been made on the basis of elemental analysis and spectral data. Th
Cobalt-, Nickel- and Copper(II) Complexes of Schiff Bases with N or S Donor Sites
Bhaskare, C. K.,Hankare, P. P.
, p. 585 - 588 (2007/10/03)
Condensation of 2-aminothiazole and its derivatives with vic-hydroxyaldehydes gives Schiff bases which form complexes of the type ML2 with bivalent transition metals.The ligand molecule both N and S donor sites and coordination through any one atom is pos
Synthesis and Biological Activity of Some Schiff Bases Derived from Thiazoles and Benzothiazoles
Dash, B.,Patra, M.,Praharaj, S.
, p. 894 - 897 (2007/10/02)
4-Aryl-2-aminothiazoles and 2-aminobenzothiazoles undergo condensation with salicylaldehyde in the presence of piperidine to give the schiff bases II and III, respectively.A similar reaction of 4-aryl-2-aminothiazole methiodides gives the schiff bases 4-aryl-2-(2'-hydroxyaryliminomethyl)thiazole methiodides (IV).Several schiff bases have been condensed with cyclohexanone and thioglycollic acid to furnish 4-aryl-2-(2'-hydroxy-α-substituted benzylamino)thiazoles (V) and 2-(2'-hydroxyphenyl) or naphthyl)-3-(4''-arylthiazol-2''-yl)-4-thiazolidones (VI), respectively.Structure elucidation of the schiff bases has been made on the basis of their elemental analyses, IR and mass spectral data.The biological screening data of the schiff bases and their metal complexes are also presented.
Kinetics of Hydrolysis of N-Salicylidene-2-amino-4-substituted-phenylthiazoles
Dash, Anadi C.,Dash, Bhaskar,Patra, Moheshwar
, p. 492 - 494 (2007/10/02)
The kinetics of hydrolysis of schiff bases, N-salicylidene-2-amino-(4-substituted phenyl)thiazoles have been investigated in 20percent ethanol-water at 30.0 +/- 0.5 deg C, pH = 4.05-5.90 and I = 0.05 mol dm-3.The reaction proceeds via uncatalys
