ARTICLE;
CHEMICAL REACTION;
COLUMN CHROMATOGRAPHY;
DRUG SYNTHESIS;
INFRARED SPECTROMETRY;
MASS SPECTROMETRY;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
ONE POT SYNTHESIS;
PRIORITY JOURNAL;
Novel inhibitor of p38 MAP kinase as an anti-TNF-α drug: Discovery of N-[4-[2-ethyl-4-(3-methylphenyl)-1,3-thiazol-5-yl]-2-pyridyl]benzamide (TAK-715) as a potent and orally active anti-rheumatoid arthritis agent
DOI 10.1021/jm050165o
S Miwatashi Y Arikawa E Kotani M Miyamoto KI Naruo H Kimura T Tanaka S Asahi S Ohkawa 2005 Novel inhibitor of p38 MAP kinase as an anti-TNF- αdrug: discovery of N-[4-[2-ethyl-4-(3-methylphenyl)-1,3-thiazol-5-yl]-2- pyridyl]benzamide (TAK-715) as a potent and orally active anti-rheumatoid arthritis agent J Med Chem 48 5966 5979 10.1021/jm050165o (Pubitemid 41324607)
Synthesis and biological evaluation of new thiazolyl/benzothiazolyl- amides, derivatives of 4-phenyl-piperazine
DOI 10.1016/j.farmac.2005.06.014, PII S0014827X05001473
C Papadopoulou A Geronikaki D Hadjipavlou-Litina 2005 Synthesis and biological evaluation of new thiazolyl/benzothiazolyl-amides, derivatives of 4-phenyl-piperazine Farmaco 60 969 973 10.1016/j.farmac.2005.06.014 (Pubitemid 41586275)
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
DOI 10.1021/jm00076a012
Y Kumar R Green KZ Borysko DS Wise LL Wotring LB Townsend 1993 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 J Med Chem 36 3843 3848 10.1021/jm00076a012 (Pubitemid 24006713)
Facile synthesis of thiazoles via an intramolecular thia-Michael strategy
Y Tsuruni H Ueda K Hayashi S Takase M Nishikawa S Kiyoto M Okuhara 1995 Facile synthesis of thiazoles via an intramolecular thia-Michael strategy J Antibiot 48 1066
Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. Synthesis and basic structure-activity relationship studies of PETT Analogs
10.1021/jm00025a010
FW Bell AS Cantrell M Hoberg SR Jaskunas NG Johansson CL Jordon MD Kinnick P Lind JM Morin B Oberg JA Palkowitz CA Parrish J Pranc H Zhang XX Zhou 1995 Phenethylthiazolethiourea (PETT) compounds, a new class of HIV-1 reverse transcriptase inhibitors. Synthesis and basic structure-activity relationship studies of PETT Analogs J Med Chem 38 4929 4936 10.1021/jm00025a010
Synthesis and biological evaluation of novel bisheterocycle-containing compounds as potential anti-influenza virus agents
DOI 10.1016/j.bmcl.2005.08.046, PII S0960894X05010735
WL Wang DY Yao M Gu MZ Fan JY Li YC Xing FJ Nan 2005 Waste-free solid-state organic syntheses: solvent-free alkylation, heterocyclization, and azo-coupling reactions Bioorg Med Chem Lett 15 5284 5287 10.1016/j.bmcl.2005.08. 046 (Pubitemid 41463665)
Efficient synthesis of 2,4-disubstituted thiazoles using ionic liquidunder ambient conditions: a practical approach towardsthesynthesis of Fanetizole
DOI 10.1016/j.tet.2007.08.036, PII S0040402007014317
TM Potewar SA Ingale KV Srinivasan 2007 Efficient synthesis of 2,4-disubstituted thiazoles using ionic liquid under ambient conditions: a practical approach towards the synthesis of Fanetizole Tetrahedron 63 11066 11069 10.1016/j.tet.2007.08.036 (Pubitemid 47464412)
(2007)Tetrahedron, vol.63, Issue.45, pp. 11066-11069
Efficient access to 5-substituted thiazoles by a novel metallotropic rearrangement
DOI 10.1016/j.tetlet.2007.11.029, PII S0040403907022058
A Zambon G Borsato S Brussolo P Frascella V Lucchini 2008 Efficient access to 5-substituted thiazoles by a novel metallotropic rearrangement Tetrahedron Lett 49 66 69 10.1016/j.tetlet.2007.11.029 (Pubitemid 350191894)
2-Amino-5-thiazolyl motif: A novel scaffold for designing anti-inflammatory agents of diverse structures
10.1016/j.ejmech.2007.02.008
PX Franklin AD Pillai PD Rathod S Yerande M Nivsarkar H Padh KK Vasu V Sudarsanam 2008 2-Amino-5-thiazolyl motif: a novel scaffold for designing anti-inflammatory agents of diverse structures Eur J Med Chem 43 129 134 10.1016/j.ejmech.2007.02.008
Synthesis of some novel 2,4-disubstituted thiazoles as possible antimicrobial agents
DOI 10.1016/j.ejmech.2007.03.014, PII S0223523407001481
P Karegoudar MS Karthikeyan DJ Prasad M Mahalinga BS Holla NS Kumari 2008 Synthesis of some novel 2,4-disubstituted thiazoles as possible antimicrobial agents Eur J Med Chem 43 261 267 10.1016/j.ejmech.2007.03.014 (Pubitemid 351222681)
M Ochiai Y Nishi S Hashimoto Y Tsuchimoto DW Chen 2003 Synthesis of 2,4-disubstituted thiazoles from (Z)-(2-acetoxyvinyl)phenyl-3-iodanes: Nucleophilic substitution of -3-iodanyl ketones with thioureas and thioamides J Org Chem 68 7887 7888 10.1021/jo020759o (Pubitemid 37186148)
N'-Substituted N-acyl- and N-imidoylthioureas. Preparation and conversion of N', N'-disubstituted compounds into 2-(N,N- disubstituted-amino)-5-thiazolyl ketones
10.1039/p19870001153
JC Brindley JM Caldwell GD Meakins SJ Plackett SJ Price 1987 N'-Substituted N-acyl- and N-imidoylthioureas. Preparation and conversion of N', N'-disubstituted compounds into 2-(N,N- disubstituted-amino)-5-thiazolyl ketones J Chem Soc, Perkin Trans 1 1153 1158 10.1039/p19870001153
Synthesis of functionalized 5-imino-2,5-dihydro-furans through the reaction of isocyanides with activated acetylenes in the presence of ethyl bromopyruvate
DOI 10.1007/s11030-006-9034-4
I Yavari Z Hossaini M Sabbaghan 2006 Synthesis of functionalized 5-imino-2,5-dihydro-furans through the reaction Mol Divers 10 479 482 10.1007/s11030-006-9034-4 (Pubitemid 46150640)
Reaction between alkyl isocyanides and isopropylidene Meldrum's acid in the presence of bidentate nucleophiles
DOI 10.1007/s11030-006-9052-2
I Yavari M Sabbaghan Z Hossaini 2007 Reaction between alkyl isocyanides and isopropylidene Meldrum's acid in the presence of bidentate nucleophiles Mol Divers 11 1 5 10.1007/s11030-006-9052-2 (Pubitemid 46639417)
Efficient synthesis of alkyl 2-[2-(arylcarbonylimino)-3-aryl-4-oxo-1, 3-thiazolan-5-ylidene]-acetates
DOI 10.1007/s11030-007-9061-9
I Yavari M Sabbaghan K Porshamsian M Bagheri S Ali-Asgari Z Hossaini 2007 Efficient synthesis of alkyl 2-[2-(arylcarbonylimino)-3-aryl-4-oxo-1,3- thiazolan-5-ylidene]-acetates Mol Divers 11 81 85 10.1007/s11030-007-9061-9 (Pubitemid 350104532)