SYNTHESIS OF 3-ARYL AND 3-HETEROCYCLIC QUINOXALIN-2-YLAMINES VIA PD-CATALYZED CROSS-COUPLING REACTIONS

[1]  C. Garner,et al.  4-(2,2-dimethyldioxalan-4-yl)-5-(quinoxalin-2-yl)-1,3-dithiol-2-one, a proligand relating to the cofactor of the oxomolybdoenzymes , 1998 .

[2]  Kiyoshi Tanaka,et al.  Synthesis of 9-(trifluoromethyl)pyrido[1′,2′:1,2]-imidazo[4,5-b]quinoxalines , 1994 .

[3]  T. Waldron,et al.  Synthesis, biological properties, and structure-activity relationships of quinoxaline angiotensin II receptor antagonists , 1993 .

[4]  G. V. Smith,et al.  Modification of Pd and Pt by Thiophene and Carbon Tetrachloride During Hydrogenation and Isomerization of (+)-Apopinene , 1993 .

[5]  Kiyoshi Tanaka,et al.  Synthesis of pyrido[1′,2′:1,2]imidazo[4,5-b]quinoxalines , 1992 .

[6]  L. S. Liebeskind,et al.  3-Stannylcyclobutenediones as nucleophilic cyclobutenedione equivalents. Synthesis of substituted cyclobutenediones and cyclobutenedione monoacetals and the beneficial effect of catalytic copper iodide on the Stille reaction , 1990 .

[7]  R. G. Browne,et al.  4-Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants. , 1990, Journal of medicinal chemistry.

[8]  G. Crisp Palladium Mediated Formation of Bithiophenes , 1989 .

[9]  H. Zimmer,et al.  Lithiation reaction of 2,5-dibromothiophene. Carbon-13 NMR spectra of 3-substituted derivatives , 1984 .

[10]  M. Kosugi,,et al.  Preparation of Aryltributyltin Having Electron-withdrawing Group by Palladium Catalyzed Reaction of Hexabutylditin with Aryl Iodide , 1983 .

[11]  E. Elslager,et al.  Potential antimalarial agents. 2-([(Dialkylamino)alkyl]amino)-3-(2-pyridyl)quinoxalines. , 1968, Journal of medicinal chemistry.