One-pot synthesis of fused-tetracyclic scaffolds employing a Lewis acid promoted domino reaction of naphthoquinones

Synthesis

Volumn , Issue 14, 2011, Pages 2321-2333

  Bendiabdellah, Yassine ^a   Villanueva Margalef, Isabel ^a   Misale, Antonio ^a   Nahar, Kazi S ^a   Haque, Mohammad R ^a   Thurston, David E ^a   Zinzalla, Giovanna ^a  

^a IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

Author keywords

intramolecular Diels Alder cycloaddition; Lewis acid promoted domino reaction; naphthoquinone; tetracyclic scaffolds

Indexed keywords

CROSS-CONJUGATED TRIENES; DIELS-ALDER CYCLOADDITIONS; DOMINO REACTIONS; FACILE SYNTHESIS; HEMIACETALS; HETEROCYCLIZATIONS; IMINE FORMATION; LEWIS ACID; MOLECULAR FRAMEWORKS; NAPHTHOQUINONE; ONE-POT SYNTHESIS; REACTION CASCADES; TETRACYCLIC SCAFFOLDS;

CYCLOADDITION; KETONES; REACTION KINETICS; SCAFFOLDS;

SYNTHESIS (CHEMICAL);

1,4 NAPHTHOQUINONE DERIVATIVE; ACETAL DERIVATIVE; FUNCTIONAL GROUP; HYDROXYL GROUP; IMINE; LEWIS ACID;

ARTICLE; CATALYSIS; CHEMICAL INTERACTION; CHEMICAL REACTION; CHEMICAL STRUCTURE; CYCLIZATION; CYCLOADDITION; DIELS ALDER REACTION; DOMINO REACTION; HETEROCYCLIZATION; ONE POT SYNTHESIS;

EID: 79960137288     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0030-1260073     Document Type: Article

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