Specific features of the reactions of quinazoline and its 4-hydroxy and 4-chloro substituted derivatives with C-nucleophiles

Tetrahedron Letters

Volumn 50, Issue 24, 2009, Pages 2899-2903

  Azev, Yuri A ^a,b   Shorshnev, Sergey V ^c   Golomolzin, Boris V ^a  

^a Ural Research Institute of Medicinal Preparation Technology   (Russian Federation)

^b URAL FEDERAL UNIVERSITY   (Russian Federation)

^c ChemBridge Corporation   (Russian Federation)

Author keywords

Nucleophiles; Quinazoline; Transformations

Indexed keywords

1 PHENYL 3 METHYLPYRAZOL 5 ONE; 1,3 DIMETHYLBARBITURIC ACID; 4 (1 PHENYL 3 METHYL 5 OXOPYRAZOL 4 YL) QUINAZOLINE; 4 (1,2,3,4, TETRAHYDRO 6 HYDROXY 1,3 DIMETHYL 2,4 DIOXOPYRIMIDIN 5 YL) 3,4 DIHYDROQUINAZOLINE; 4 (2 METHYLINDOL 3 YL) QUINAZOLINE; 4 (2,3,4 TRIHYDROXYPHENYL) 3,4 DIHYDROQUINAZOLINE; 4 (INDOL 3 YL) 3,4 DIHYDROQUINAZOLINE; 4 CHLOROQUINAZOLINE; BARBITURIC ACID; DIPYRAZOLYLMETHANE; INDOLE; METHANE; NUCLEOPHILE; PYRAZOLE DERIVATIVE; PYROGALLOL; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; SUBSTITUTION REACTION;

EID: 65249153588     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.03.199     Document Type: Article

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