2-(Diethylamino)thieno[1,3]oxazin-4-ones as Stable Inhibitors of Human Leukocyte Elastase, Journal of Medicinal Chemistry, vol.42, issue.26, pp.5437-5447, 1999. ,
DOI : 10.1021/jm991108w
Isothiocyanates in the chemistry of heterocycles, Chemical Reviews, vol.91, issue.1, pp.1-24, 1991. ,
DOI : 10.1021/cr00001a001
)-ones, The Journal of Organic Chemistry, vol.72, issue.1, pp.284-287, 2007. ,
DOI : 10.1021/jo0618066
Synthesis and antileishmanial activity of (1,3-benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives, European Journal of Medicinal Chemistry, vol.39, issue.8, pp.685-690, 2004. ,
DOI : 10.1016/j.ejmech.2004.04.006
Benzothiazole derivatives substituted in position 2 as biologically active substances with plant growth regulation activity, Plant, Soil and Environment, vol.51, issue.No. 11, pp.496-505, 2005. ,
DOI : 10.17221/3623-PSE
Antitumour benzothiazoles. Part 10: The synthesis and antitumour activity of benzothiazole substituted quinol derivatives, Bioorganic & Medicinal Chemistry Letters, vol.10, issue.5, pp.513-515, 2000. ,
DOI : 10.1016/S0960-894X(00)00027-5
Comprehensive heterocyclic chemistry, p.302 ,
Ueber Bildung von Anhydroverbindungen des Orthoamidophenylmercaptans aus Thioaniliden, Berichte der deutschen chemischen Gesellschaft, vol.207, issue.1, p.1067 ,
DOI : 10.1002/cber.188601901239
1éq) de thio-urée sont dissous N -(4-Méthoxyphényl)-4,5-dihydronaphto[1,2-b]thiéno[3,2-d][1,3]thiazol-2-amine (141) Rendement: 62 % Aspect: solide brun Point de fusion: 135 °C RMN 1 H (250 MHz, Hz, vol.100, issue.9, pp.5-8632516191195 ,
A 3D QSAR Model of 17??-HSD1 Inhibitors Based on a Thieno[2,3-d]pyrimidin-4(3H)-one Core Applying Molecular Dynamics Simulations and Ligand???Protein Docking, ChemMedChem, vol.18, issue.3, p.461, 2008. ,
DOI : 10.1007/s008940100045
Synthesis of azo benzo[b]thiophene derivatives and their application as disperse dyes, Dyes and Pigments, vol.10, issue.4, p.295, 1989. ,
DOI : 10.1016/0143-7208(89)85017-X
Heterocyclen aus CH-aciden Nitrilen, VII. 2-Amino-thiophene aus ??-Oxo-mercaptanen und methylenaktiven Nitrilen, Chemische Berichte, vol.659, issue.11, p.3571, 1965. ,
DOI : 10.1002/cber.19650981120
Heterocyclen aus CH-aciden Nitrilen, VIII. 2-Amino-thiophene aus methylenaktiven Nitrilen, Carbonylverbindungen und Schwefel, Chemische Berichte, vol.1963, issue.1, p.94, 1966. ,
DOI : 10.1002/cber.19660990116
Synth??se d'amino-3 thioph??nes a partir d'aryl-et d'h??taryl-ac??tonitrile, Journal of Heterocyclic Chemistry, vol.13, issue.3, p.443, 1982. ,
DOI : 10.1002/jhet.5570190248
Substituted 3-amino-thiophenes and 3-amino-selenophenes from ?-chloro-?-cyano-cinnamonitrile, Monatshefte f???r Chemie Chemical Monthly, vol.95, issue.5, p.455, 1992. ,
DOI : 10.1007/BF00817601
In the chemistry of cyano group; Rappoport, Z, 1979. ,
phosphorus sulfur, and silicon, p.91, 1993. ,
Synth??se d'amino-3 thioph??nes a partir d'aryl-et d'h??taryl-ac??tonitrile, Journal of Heterocyclic Chemistry, vol.13, issue.3, p.443, 1982. ,
DOI : 10.1002/jhet.5570190248
A 3D QSAR Model of 17??-HSD1 Inhibitors Based on a Thieno[2,3-d]pyrimidin-4(3H)-one Core Applying Molecular Dynamics Simulations and Ligand???Protein Docking, ChemMedChem, vol.18, issue.3, p.461, 2008. ,
DOI : 10.1007/s008940100045
Reversible Inhibitors of the Gastric (H+/K+)-ATPase. 5. Substituted 2,4-Diaminoquinazolines and Thienopyrimidines, Journal of Medicinal Chemistry, vol.38, issue.14, p.2763, 1995. ,
DOI : 10.1021/jm00014a027
Acetylcholinesterase inhibition by fused dihydroquinazoline compounds, Bioorganic & Medicinal Chemistry Letters, vol.6, issue.6, p.737, 1996. ,
DOI : 10.1016/0960-894X(96)00102-3
Beckmann Rearrangement of Oximes under Very Mild Conditions, The Journal of Organic Chemistry, vol.67, issue.17, p.6272, 2002. ,
DOI : 10.1021/jo025960d
)-ones, The Journal of Organic Chemistry, vol.72, issue.1, p.284, 2007. ,
DOI : 10.1021/jo0618066
Benzimidazo[2,1-b]quinazolin-12-ones. New class of potent immunosuppressive compounds, Journal of Medicinal Chemistry, vol.14, issue.11, p.1069, 1971. ,
DOI : 10.1021/jm00293a012
2-(Diethylamino)thieno[1,3]oxazin-4-ones as Stable Inhibitors of Human Leukocyte Elastase, Journal of Medicinal Chemistry, vol.42, issue.26, p.5437, 1999. ,
DOI : 10.1021/jm991108w
Building a model of interaction at the NK-2 receptors: Polycondensed heterocycles containing the pyrimidoindole skeleton, European Journal of Medicinal Chemistry, vol.32, issue.12, p.973, 1997. ,
DOI : 10.1016/S0223-5234(97)89641-9
Synthesis and antimicrobial activity of novel 2-thiazolylimino-5-arylidene-4-thiazolidinones, Bioorganic & Medicinal Chemistry, vol.14, issue.11, p.3859, 2006. ,
DOI : 10.1016/j.bmc.2006.01.043
Synthesis and antileishmanial activity of (1,3-benzothiazol-2-yl) amino-9-(10H)-acridinone derivatives, European Journal of Medicinal Chemistry, vol.39, issue.8, p.685, 2004. ,
DOI : 10.1016/j.ejmech.2004.04.006
Antitumour benzothiazoles. Part 10: The synthesis and antitumour activity of benzothiazole substituted quinol derivatives, Bioorganic & Medicinal Chemistry Letters, vol.10, issue.5, p.513, 2000. ,
DOI : 10.1016/S0960-894X(00)00027-5
Ueber Bildung von Anhydroverbindungen des Orthoamidophenylmercaptans aus Thioaniliden, Berichte der deutschen chemischen Gesellschaft, vol.207, issue.1, p.1067 ,
DOI : 10.1002/cber.188601901239
Facile synthesis of thiourea derivatives in ionic liquid, Chinese Chemical Letters, vol.18, issue.3, p.258, 2007. ,
DOI : 10.1016/j.cclet.2007.01.036
Synthesis, spectroscopic characterization, crystal structure and pharmacological properties of some novel thiophene-thiourea core derivatives, European Journal of Chemistry, vol.1, issue.3, p.221, 2010. ,
DOI : 10.5155/eurjchem.1.3.221-227.124
A convenient access to substituted benzothiazole scaffolds via intramolecular cyclization of thioformanilides, Tetrahedron Letters, vol.48, issue.4, p.669, 2007. ,
DOI : 10.1016/j.tetlet.2006.11.105
accès à partir des dérivés amino-ester aux dérivés aminés nous a permis la construction de nouveaux systèmes hétérocycliques substituant du noyau thiophénique tels les 2-chloro N-(3-thiényl) acétamides, isothiocyanates et N-(3-thiényl) thio-urée, utilisés pour la synthèse des systèmes condensés tels les 1,3-thiazolidinones et les thiéno, p.3 ,