A green synthesis of quinoxalines and 2,3-dihydropyrazines

Synthesis (Germany)

Volumn 45, Issue 11, 2013, Pages 1546-1552

  Delpivo, Camilla ^a   Micheletti, Gabriele ^a   Boga, Carla ^a  

^a Department of Industrial Chemistry 'Toso Montanari' ^*  (Italy)

Author keywords

condensation; dihydropyrazine; green; quinoxaline; water

Indexed keywords

DIHYDROPYRAZINE; GREEN; GREEN SYNTHESIS; HIGH YIELD; MILD REACTION CONDITIONS; MOTHER LIQUOR; QUINOXALINES; REACTION MIXTURE;

CHEMISTRY; SPEECH SYNTHESIS; WATER;

CONDENSATION;

2 ETHYL 3 METHYL 4A,5,6,7,8,8A HEXAHYDROQUINOXALINE; 2 ETHYL 3,6 DIMETHYLQUINOXALINE; 2 METHYL 3 PHENYL 4A,5,6,7,8,8A HEXAHYDROQUINOXALINE; 2 METHYL 3 PROPYL 4A,5,6,7,8,8A HEXAHYDROQUINOXALINE; 2,3 DIETHYL 4A,5,6,7,8,8A HEXAHYDROQUINOXALINE; 2,3 DIHYDROXYPYRAZINE; 2,5 DIMETHYL 6 PHENYL 2,3 DIHYDROPYRAZINE; 2,5 DIMETHYL 6 PROPYL 2,3 DIHYDROPYRAZINE; 2,6 DIMETHYL 3 PHENYLQUINOXALINE; 2,6 DIMETHYL 3 PROPYLQUINOXALINE; 2,6 DIMETHYL 5 PHENYL 2,3 DIHYDROPYRAZINE; 2,6 DIMETHYL 5 PROPYL 2,3 DIHYDROPYRAZINE; 3 ETHYL 2,6 DIMETHYLQUINOXALINE; 3,6 DIMETHYL 2 PHENYLQUINOXALINE; 3,6 DIMETHYL 2 PROPYLQUINOXALINE; 5 ETHYL 2,6 DIMETHYL 2,3 DIHYDROPYRAZINE; 5,6 DIETHYL 2 METHYL 2,3 DIHYDROPYRAZINE; 6 CHLORO 2 ETHYL 3 METHYLQUINOXALINE; 6 CHLORO 2 METHYL 3 PHENYLQUINOXALINE; 6 CHLORO 2 METHYL 3 PROPYLQUINOXALINE; 6 CHLORO 3 ETHYL 2 METHYLQUINOXALINE; 6 CHLORO 3 METHYL 2 PHENYLQUINOXALINE; 6 CHLORO 3 METHYL 2 PROPYLQUINOXALINE; 6 ETHYL 2,5 DIMETHYL 2,3 DIHYDROPYRAZINE; CARBON NITROGEN MONOCYCLE; FUSED CARBON NITROGEN HETEROCYCLE; PYRAZINE DERIVATIVE; QUINOXALINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYST; CHEMICAL ANALYSIS; CHEMICAL PARAMETERS; CHEMICAL STRUCTURE; CONCENTRATION (PARAMETERS); GREEN CHEMISTRY; MASS SPECTROMETRY; PRECIPITATION; PROCESS DEVELOPMENT; PRODUCT YIELD; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION TIME; ROOM TEMPERATURE; SOLUBILITY; TEMPERATURE DEPENDENCE; TEMPERATURE SENSITIVITY; THERMAL ANALYSIS;

EID: 84878123751     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0033-1338441     Document Type: Article

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