59352-87-3Relevant articles and documents
Synthesis of quinoxalines and pyrido[2,3-b]pyrazines by SuzukiMiyaura cross-coupling reaction
Kumbhar, Arjun,Jadhav, Sanjay,Salunkhe, Rajashri
, p. 5431 - 5440 (2016/06/01)
Abstract: Bromo-substituted quinoxalines and pyrido[2,3-b]pyrazines were synthesized by condensation reactions of aromatic 1,2-diamino and 1,2-diketone compounds. These compounds were used as common intermediates for postcondensation modification by SuzukiMiyaura coupling reaction to form aryl-substituted quinoxalines and pyrido[2,3-b]pyrazines. High-efficiency with improved product yield of aryl-substituted quinoxalines and pyrido[2,3-b]pyrazine derivatives was achieved by conducting a coupling reaction in presence of Pd(dppf)Cl2·CH2Cl2 in tetrahydrofuran (THF) using K2CO3 as base at reflux temperature. Graphical abstract: [Figure not available: see fulltext.].
Palladium-catalyzed cross-coupling reactions of 7-bromo-2,3-diphenyl- pyrido[2,3-b]pyrazine
Yin, Lunxiang,Liebscher, Juergen
, p. 1345 - 1349 (2007/10/03)
First examples of palladium-catalyzed cross-coupling reactions, such as Suzuki, Sonogashira, Heck and Buchwald-Hartwig reactions, are reported in the pyrido[2,3-b]pyrazine series. This methodology circumvents problems found in uncatalyzed nucleophilic sub