A facile phenol-driven intramolecular diastereoselective thermal/base-catalyzed dipolar [2 + 2] annulation reactions: An easy access to complex bioactive natural and unnatural benzopyran congeners

Journal of Organic Chemistry

Volumn 72, Issue 6, 2007, Pages 2068-2076

  Mondal, Mukulesh ^a   Puranik, Vedavati G ^a   Argade, Narshinha P ^a  

^a NATIONAL CHEMICAL LABORATORY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

BENZOPYRAN; CARBONYL MOIETY; CONGENERS; DIHYDROXYPHTHALIDES;

BIOACTIVITY; CARBOXYLIC ACIDS; CYCLIZATION; DERIVATIVES; STEREOSELECTIVITY; SYNTHESIS (CHEMICAL);

AROMATIC COMPOUNDS;

BENZOPHENONE DERIVATIVE; BENZOPYRAN DERIVATIVE; DIHYDROXYPHTHALIDE DERIVATIVE; PHENOL DERIVATIVE; PHTHALIDE DERIVATIVE; RESORCYCLIC ACID DERIVATIVE; TRIHYDROXYBENZOPHENONE; UNCLASSIFIED DRUG;

ANNULATION REACTION; ARTICLE; CATALYSIS; CHEMICAL REACTION KINETICS; COMPLEX FORMATION; ENANTIOMER; HYDROGEN BOND; PRODUCT RECOVERY; REACTION ANALYSIS; STRUCTURE ACTIVITY RELATION; THERMAL ANALYSIS; THERMODYNAMICS;

BENZOPYRANS; BIOLOGICAL PRODUCTS; CATALYSIS; HEAT; PHENOL; STEREOISOMERISM;

EID: 33947206729     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0624344     Document Type: Article

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