Copper-catalyzed domino synthesis of quinazolin-4(3 H)-ones from (Hetero)arylmethyl halides, bromoacetate, and cinnamyl bromide

Synthesis (Germany)

Volumn 45, Issue 24, 2013, Pages 3349-3354

  Wei, Haidong ^a   Li, Tianbin ^a   Zhou, Yue ^a   Zhou, Lihong ^a   Zeng, Qingle ^a  

^a CHENGDU UNIVERSITY OF TECHNOLOGY   (China)

Author keywords

condensation; copper; oxygenation; quinazolin 4(3 H) ones; tandem reaction

Indexed keywords

ALKYL HALIDES; CINNAMYL BROMIDE; COPPER BROMIDE; DOMINO REACTIONS; GREEN PROCESS; HETEROCYCLES; QUINAZOLIN-4(3 H)-ONES; TANDEM REACTION;

CATALYSIS; CONDENSATION; FUNCTIONAL GROUPS; OXYGENATION; REACTION KINETICS;

COPPER;

2 (3 FLUOROPHENYL)BENZOFURO[3,2 D]PYRIMIDIN 4[3H]ONE; 2 (M TOLYL)BENZOFURO[3,2 D]PYRIMIDIN 4[3H]ONE; 3 (4 OXO 3,4-DIHYDROQUINAZOLIN 2 YL)BENZONITRILE; 6 CHLORO 2 (2 FLUOROPHENYL)QUINAZOLIN 4[3H]ONE; 6 CHLORO 2 [4 (TRIFLUOROMETHYL)PHENYL]QUINAZOLIN 4[3H]ONE; BROMOACETIC ACID; CINNAMIC ACID DERIVATIVE; CINNAMYLBROMIDE; COPPER BROMIDE; COPPER DERIVATIVE; ETHYL 4 (4 OXO 3,4 DIHYDROQUINAZOLIN 2 YL)BENZOATE; HALIDE; HETEROARYLMETHYLHALIDE DERIVATIVE; QUINAZOLIN 4[3H]ONE DERIVATIVE; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL ANALYSIS; CHEMICAL COMPOSITION; CHEMICAL INTERACTION; CHEMICAL STRUCTURE; HALOGENATION; OXIDATION; REACTION TIME; SOLVENT EFFECT; SUBSTITUTION REACTION; SYNTHESIS; TEMPERATURE SENSITIVITY;

EID: 84889883670     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0033-1340040     Document Type: Article

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