Construction of a C(30-38) dioxabicyclo[3.2.1]octane subtarget for (+)-sorangicin A, exploiting a regio- and stereocontrolled acid-catalyzed epoxide ring opening

Organic Letters

Volumn 6, Issue 9, 2004, Pages 1477-1480

  Smith III, Amos B ^a   Fox, Richard J ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACID; ALKYNE; BICYCLO COMPOUND; COBALT DERIVATIVE; DIOXABICYCLO[3.2.1]OCTANE; EPOXIDE; MACROLIDE; OCTANE; SORANGICIN A; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; COMPLEX FORMATION; DRUG POTENCY; DRUG STRUCTURE; DRUG SYNTHESIS; RING OPENING; STEREOCHEMISTRY;

ACIDS; AMINOGLYCOSIDES; BICYCLO COMPOUNDS, HETEROCYCLIC; CATALYSIS; EPOXY COMPOUNDS; MOLECULAR CONFORMATION; STEREOISOMERISM;

EID: 2442512129     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol049644s     Document Type: Article

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