Synthesis, anti-bacterial and anti-fungal activities of some novel Schiff bases containing 2,4-disubstituted thiazole ring.
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[1] B. S. Holla,et al. Synthesis of some novel 2,4-disubstituted thiazoles as possible antimicrobial agents. , 2008, European journal of medicinal chemistry.
[2] T. M. Potewar,et al. Efficient synthesis of 2,4-disubstituted thiazoles using ionic liquid under ambient conditions: a practical approach towards the synthesis of Fanetizole , 2007 .
[3] M. P. Kaushik,et al. An efficient method for the synthesis of 2-aminothiazoles using silica chloride as a heterogeneous catalyst , 2007 .
[4] K. Güven,et al. Synthesis and antimicrobial activity of 1-(4-aryl-2-thiazolyl)-3-(2-thienyl)-5-aryl-2-pyrazoline derivatives. , 2007, European journal of medicinal chemistry.
[5] G. Kabalka,et al. Microwave promoted synthesis of functionalized 2-aminothiazoles , 2006 .
[6] B. Das,et al. A rapid and high-yielding synthesis of thiazoles and aminothiazoles using ammonium-12-molybdophosphate , 2006 .
[7] A. Iqbal,et al. Synthesis and spectroscopic studies of new Schiff bases. , 2006, Molecules.
[8] V. Borisenko,et al. Hydrogen bonds of 2-aminothiazoles in intermolecular complexes (1:1 and 1:2) with proton acceptors in solutions , 2006 .
[9] I. Yilmaz,et al. Synthesis, antibacterial and antifungal activity of some new thiazolylhydrazone derivatives containing 3-substituted cyclobutane ring. , 2006, European journal of medicinal chemistry.
[10] K. R. Rao,et al. Aqueous phase synthesis of thiazoles and aminothiazoles in the presence of β-cyclodextrin , 2005 .
[11] Jamil Anwar Choudary,et al. An Efficient Synthesis of 2-Alkyl-4-hydroxy-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxides , 2005 .
[12] A. Dömling,et al. New MCRs: The first 4-component reaction leading to 2,4-disubstituted thiazoles , 2004, Molecular Diversity.
[13] M. V. R. D. Souza,et al. Drogas anti-VIH: passado, presente e perspectivas futuras , 2003 .
[14] B. Kamieński,et al. Spectroscopic studies of Schiff bases of 2,2′-dihydroxybiphenyl-3-carbaldehyde and para substituted anilines , 2003 .
[15] B. S. Holla,et al. Synthesis of some new 2,4-disubstituted thiazoles as possible antibacterial and anti-inflammatory agents. , 2003, European journal of medicinal chemistry.
[16] S. E. Kazzouli,et al. Solid support synthesis of 2,4-disubstituted thiazoles and aminothiazoles , 2002 .
[17] Yi-zhi Li,et al. Antitumour activity of transition metal complexes with the thiosemicarbazone derived from 3-acetylumbelliferone , 2001 .
[18] R. DesJarlais,et al. Synthesis of thiophene-2-carboxamidines containing 2-aminothiazoles and their biological evaluation as urokinase inhibitors. , 2001, Bioorganic & medicinal chemistry letters.
[19] A. IJzerman,et al. Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists. , 2001, Journal of medicinal chemistry.
[20] T. Hagen,et al. 2,4-Disubstituted oxazoles and thiazoles as latent pharmacophores for diacylhydrazine of SC-51089, a potent PGE2 antagonist. , 2001, Bioorganic & medicinal chemistry.
[21] K. Erol,et al. Synthesis of some thiazolyl-pyrazoline derivatives and preliminary investigation of their hypotensive activity. , 2000, European journal of medicinal chemistry.
[22] B. Jiang,et al. Syntheses and cytotoxicity evaluation of bis(indolyl)thiazole, bis(indolyl)pyrazinone and bis(indolyl)pyrazine: analogues of cytotoxic marine bis(indole) alkaloid. , 2000, Bioorganic & medicinal chemistry.
[23] J. Leger,et al. New 2-sulfonamidothiazoles substituted at C-4: synthesis of polyoxygenated aryl derivatives and in vitro evaluation of antifungal activity , 1999 .
[24] D. Holt,et al. Structure-based design and synthesis of a novel class of Src SH2 inhibitors. , 1999, Bioorganic & medicinal chemistry letters.
[25] J. Katzenellenbogen,et al. Novel structural templates for estrogen-receptor ligands and prospects for combinatorial synthesis of estrogens. , 1999, Chemistry & biology.
[26] X. Wan,et al. Syntheses and biological activities of bis(3-indolyl)thiazoles, analogues of marine bis(indole)alkaloid nortopsentins. , 1999, Bioorganic & medicinal chemistry letters.
[27] A. Revol-Junelles,et al. Leuconostoc mesenteroides subsp. mesenteroides FR52 synthesizes two distinct bacteriocins , 1996, Letters in applied microbiology.
[28] A. M. Al-Obaid,et al. 2,4-Disubstituted thiazoles II. A novel class of antitumor agents, synthesis and biological evaluation , 1996 .
[29] Alan R. Katritzky,et al. Comprehensive Heterocyclic Chemistry IV , 1996 .
[30] J M Morin,et al. Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. 1. Synthesis and basic structure-activity relationship studies of PETT analogs. , 1995, Journal of medicinal chemistry.
[31] H. Ishikawa,et al. Synthesis and anti-pseudomonal activity of new 2-isocephems with a dihydroxypyridone moiety at C-7 , 1994 .
[32] Y. Kumar,et al. Synthesis of 2,4-disubstituted thiazoles and selenazoles as potential antitumor and antifilarial agents: 1. Methyl 4-(isothiocyanatomethyl)thiazole-2-carbamates, -selenazole-2- carbamates, and related derivatives. , 1993, Journal of medicinal chemistry.
[33] Y. Kumar,et al. Synthesis of 2,4-disubstituted thiazoles and selenazoles as potential antifilarial and antitumor agents. 2. 2-Arylamido and 2-alkylamido derivatives of 2-amino-4-(isothiocyanatomethyl)thiazole and 2-amino-4-(isothiocyanatomethyl)selenazole. , 1993, Journal of medicinal chemistry.
[34] A. Doherty,et al. Structure-activity relationships of a series of 2-amino-4-thiazole-containing renin inhibitors. , 1992, Journal of medicinal chemistry.
[35] M. S. South,et al. Reactions of a 4‐(trifluoromethyl)thiazole dianion , 1991 .
[36] M. S. South. Synthesis and reactions of halogenated thiazole isocyanates , 1991 .
[37] Kiyoshi Tanaka,et al. Synthesis of trifluoromethylthiazoles and their application to azo dyes , 1991 .
[38] A. Haemers,et al. Quinolone antibacterials : 2. 6-substituted-7-(2-thiazolyl)quinolones and 6-substituted-7-(2-thiazolidinyl)quinolones , 1991 .
[39] P. Young,et al. 3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives: inhibitors of immune complex induced inflammation. , 1988, Journal of medicinal chemistry.
[40] R. Bergstrom,et al. Nizatidine, an H2-blocker. Its metabolism and disposition in man. , 1986, Drug metabolism and disposition: the biological fate of chemicals.
[41] J. Tuite. Plant pathological methods : fungi and bacteria , 1970 .
[42] D. D. Perrin,et al. Purification of laboratory chemicals , 1966 .
[43] Ronald Breslow,et al. On the Mechanism of Thiamine Action. IV.1 Evidence from Studies on Model Systems , 1958 .
[44] A. Hantzsch,et al. Ueber Verbindungen des Thiazols (Pyridins der Thiophenreihe) , 1887 .