General diastereoselective synthetic approach toward isospongian diterpenes. Synthesis of (-)-marginatafuran, (-)-marginatone, and (-)-20-acetoxymarginatone

Journal of Organic Chemistry

Volumn 77, Issue 13, 2012, Pages 5664-5680

  Gris, Antonio ^a   Cabedo, Nuria ^b   Navarro, Ismael ^a   De Alfonso, Ignacio ^a   Agulló, Consuelo ^a   Abad Somovilla, Antonio ^a  

^a UNIVERSITY OF VALENCIA   (Spain)

^b UNIVERSITAT POLITÈCNICA DE VALÈNCIA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CARBOCYCLIC SKELETON; CARVONE; DIASTEREOSELECTIVE; DIELS-ALDER; DITERPENES; ELECTRON-TRANSFER CHAIN; INHIBITORY ACTIVITY; MICROMOLAR RANGE; MITOCHONDRIAL RESPIRATORY CHAIN; MONOTERPENES; NADH OXIDASE; RING-CLOSING METATHESIS REACTIONS; SYNTHETIC APPROACH; SYNTHONS;

CHEMISTRY; ORGANIC COMPOUNDS;

MAMMALS;

20 ACETOXYMARGINATONE; DITERPENE; MARGINATAFURAN; MARGINATONE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; UNCLASSIFIED DRUG;

ANNULATION REACTION; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DIASTEREOISOMER; DIELS ALDER REACTION; DRUG SYNTHESIS; ELECTRON TRANSPORT; ENZYME ACTIVITY; IC 50; NUCLEAR OVERHAUSER EFFECT; OXYGENATION; PROTON NUCLEAR MAGNETIC RESONANCE; RESPIRATORY CHAIN; RING CLOSING METATHESIS; STEREOCHEMISTRY;

DITERPENES; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 84863611036     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo3008034     Document Type: Article

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