Biginelli and Hantzsch-type reactions leading to highly functionalized dihydropyrimidinone, thiocoumarin, and pyridopyrimidinone frameworks via ring annulation with β-oxodithioesters

Journal of Organic Chemistry

Volumn 75, Issue 22, 2010, Pages 7785-7795

  Nandi, Ganesh Chandra ^a   Samai, Subhasis ^a   Singh, Maya Shankar ^a  

^a BANARAS HINDU UNIVERSITY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC ALDEHYDE; CYCLOCONDENSATION; DI-HYDROPYRIMIDINONES; DIVERSITY-ORIENTED SYNTHESIS; FUNCTIONALIZED; HIGH YIELD; NEW STRATEGY; ONE POT; OXODITHIOESTERS; REACTION CONDITIONS; SALICYLALDEHYDE; THIOCOUMARIN; THIONES; THREE-COMPONENT;

ALDEHYDES; IONIC LIQUIDS; SILICON COMPOUNDS; UREA;

SYNTHESIS (CHEMICAL);

CHROMENE DERIVATIVE; COUMARIN DERIVATIVE; HETEROCYCLIC COMPOUND; PYRIMIDINONE DERIVATIVE; SALICYLALDEHYDE; SILICON DIOXIDE; SULFURIC ACID; THIOESTER; UREA;

ANNULATION REACTION; ARTICLE; BIGINELLI REACTION; CHEMICAL REACTION; CYCLIZATION; HANTZSCH REACTION; ONE POT SYNTHESIS; POLYMERIZATION; REACTION ANALYSIS; REACTION OPTIMIZATION;

CATALYSIS; COUMARINS; HETEROCYCLIC COMPOUNDS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; PYRIMIDINONES; SULFHYDRYL COMPOUNDS; URACIL;

EID: 78449261907     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo101572c     Document Type: Article

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