Auto-redox reaction: Tin(II) chloride-mediated one-step reductive cyclization leading to the synthesis of novel biheterocyclic 5,6-dihydro-quinazolino[4,3-b]quinazolin-8-ones with three-point diversity

Journal of Organic Chemistry

Volumn 71, Issue 1, 2006, Pages 382-385

  Roy, Abhijeet Deb ^a   Subramanian, Arunachalam ^a   Roy, Raja ^a  

^a CENTRAL DRUG RESEARCH INSTITUTE   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; PHASE TRANSITIONS; REDUCTION; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL); TIN COMPOUNDS;

AUTO-REDOX REACTIONS; REDUCTIVE CYCLIZATION; REDUCTIVE TRANSFORMATIONS;

REDOX REACTIONS;

ALCOHOL DERIVATIVE; BENZENE DERIVATIVE; BICYCLO COMPOUND; HETEROCYCLIC COMPOUND; QUINAZOLINE DERIVATIVE; TIN CHLORIDE;

ARTICLE; BIOTRANSFORMATION; CYCLIZATION; OXIDATION REDUCTION REACTION; QUANTUM YIELD; REACTION ANALYSIS; REDUCTION; STEREOCHEMISTRY; SYNTHESIS;

CHLORIDES; CYCLIZATION; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; OXIDATION-REDUCTION; QUINAZOLINES; TIN;

EID: 31144434120     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0518912     Document Type: Article

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