Aqueous phase synthesis of thiazoles and aminothiazoles in the presence of β-cyclodextrin

[1]  K. R. Rao,et al.  A facile regioselective ring opening of aziridines to haloamines using tetrabutylammonium halides in the presence of β-cyclodextrin in water , 2004 .

[2]  K. R. Rao,et al.  Highly selective oxidative cleavage of beta-cyclodextrin-epoxide/aziridine complexes with IBX in water. , 2003, The Journal of organic chemistry.

[3]  K. R. Rao,et al.  Highly regioselective ring opening of oxiranes with phenoxides in the presence of beta-cyclodextrin in water. , 2003, The Journal of organic chemistry.

[4]  K. R. Rao,et al.  Mild oxidation of alcohols with o-iodoxybenzoic acid (IBX) in water/acetone mixture in the presence of beta-cyclodextrin. , 2003, The Journal of organic chemistry.

[5]  K. R. Rao,et al.  Highly efficient deprotection of aromatic acetals under neutral conditions using beta-cyclodextrin in water. , 2003, The Journal of organic chemistry.

[6]  S. E. Kazzouli,et al.  Solid support synthesis of 2,4-disubstituted thiazoles and aminothiazoles , 2002 .

[7]  A. IJzerman,et al.  Thiazole and thiadiazole analogues as a novel class of adenosine receptor antagonists. , 2001, Journal of medicinal chemistry.

[8]  J. Lewis.  Miscellaneous alkaloids: Amaryllidaceae, Sceletium, muscarine, imidazole, oxazole, peptide and other miscellaneous alkaloids , 1999 .

[9]  J. Katzenellenbogen,et al.  Novel structural templates for estrogen-receptor ligands and prospects for combinatorial synthesis of estrogens. , 1999, Chemistry & biology.

[10]  D. Goff,et al.  THE PREPARATION OF 2,4-DISUBSTITUTED THIAZOLES ON SOLID SUPPORT , 1999 .

[11]  J. Flygare,et al.  Solid-Phase Synthesis of 2-Aminothiazoles. , 1998, The Journal of organic chemistry.

[12]  A. Baxter.  Synthesis utilizing insoluble polymers: new reactions and small molecules. , 1997, Current opinion in chemical biology.

[13]  Jean-Marie Lehn,et al.  Comprehensive Supramolecular Chemistry , 1996 .

[14]  A. W. Dean,et al.  A convenient procedure for the solution phase preparation of 2-aminothiazole combinatorial libraries , 1996 .

[15]  Alan R. Katritzky,et al.  Comprehensive Heterocyclic Chemistry IV , 1996 .

[16]  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.

[17]  H. Ishikawa,et al.  Synthesis and anti-pseudomonal activity of new 2-isocephems with a dihydroxypyridone moiety at C-7 , 1994 .

[18]  D. Rich,et al.  Peptidomimetics derived from natural products , 1993, Medicinal research reviews.

[19]  A. Doherty,et al.  Structure-activity relationships of a series of 2-amino-4-thiazole-containing renin inhibitors. , 1992, Journal of medicinal chemistry.

[20]  T. Heffner,et al.  4-(1,2,5,6-Tetrahydro-1-alkyl-3-pyridinyl)-2-thiazolamines: a novel class of compounds with central dopamine agonist properties. , 1990, Journal of medicinal chemistry.

[21]  P. Young,et al.  3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives: inhibitors of immune complex induced inflammation. , 1988, Journal of medicinal chemistry.

[22]  S. Jouquey,et al.  4-Hydroxy-3-quinolinecarboxamides with antiarthritic and analgesic activities. , 1988, Journal of medicinal chemistry.

[23]  K. D. Hargrave,et al.  N-(4-substituted-thiazolyl)oxamic acid derivatives, a new series of potent, orally active antiallergy agents. , 1983, Journal of medicinal chemistry.