Enantioselective synthesis of the dioxabicyclo[3.2.1]octane core of the zaragozic acids via intramolecular Wacker-type cyclisation reactions

Organic and Biomolecular Chemistry

Volumn 2, Issue 15, 2004, Pages 2220-2228

  Perlmutter, Patrick ^a   Selajerern, Walailak ^a   Vounatsos, Filisaty ^a  

^a MONASH UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIKNOCK RATING; BIOSYNTHESIS; CHOLESTEROL; CRYSTAL STRUCTURE; ENZYME INHIBITION; FUNGI; HYDROPHOBICITY; METABOLITES; OPTIMIZATION; PROTEINS;

ENANTIOSELECTIVE SYNTHESIS; PICOMOLAR INHIBITION; WACKER-TYPE CYCLISATION REACTIONS; ZARAGOZIC ACIDS;

CARBOXYLIC ACIDS;

FUNGI;

ANTIFUNGAL AGENT; FUSED HETEROCYCLIC RINGS; OCTANE; SQUALENE SYNTHASE; ZARAGOZIC ACID C;

ARTICLE; CHEMICAL STRUCTURE; CYCLIZATION; DRUG ANTAGONISM; STEREOISOMERISM; SYNTHESIS;

ANTIFUNGAL AGENTS; BICYCLO COMPOUNDS, HETEROCYCLIC; CYCLIZATION; FARNESYL-DIPHOSPHATE FARNESYLTRANSFERASE; MOLECULAR STRUCTURE; OCTANES; STEREOISOMERISM;

EID: 4344607829     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b406280a     Document Type: Article

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