Studies for the synthesis of xenicane diterpenes. A stereocontrolled total synthesis of 4-hydroxydictyolactone

Journal of the American Chemical Society

Volumn 131, Issue 25, 2009, Pages 9038-9045

  Williams, David R ^a   Walsh, Martin J ^a   Miller, Nathan A ^a  

^a INDIANA UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLYLATION; CLAISEN REARRANGEMENT; DIRECT ACCESS; DITERPENE; DITERPENES; ENOLATE; FORMATE ESTER; FUNCTIONALIZED; IRELAND; LACTOLS; NATURAL PRODUCTS; OXIDATIVE ELIMINATION; PHENYLSELENYLATION; PROPARGYLATION; REGIO-SELECTIVE; STEREOSELECTIVE FORMATION; SUZUKI CROSS COUPLING REACTIONS; SYNTHESIS STRATEGY; TERMINAL ALKYNE; TOTAL SYNTHESIS;

ACETYLENE; ESTERIFICATION; ETHERS; OLEFINS; SILANES; STEREOCHEMISTRY;

ESTERS;

4 HYDROXYDICTYOLACTONE; NATURAL PRODUCT; UNCLASSIFIED DRUG;

ALLYLATION; ARTICLE; CHEMICAL STRUCTURE; DRUG STRUCTURE; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE; NUCLEAR OVERHAUSER EFFECT; STEREOCHEMISTRY; SUZUKI REACTION;

DITERPENES; MOLECULAR STRUCTURE; STEREOISOMERISM;

EID: 67649647688     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja902677t     Document Type: Article

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