A convergent coupling strategy for the formation of polycyclic ethers: Stereoselective synthesis of the BCDE fragment of brevetoxin A

Organic Letters

Volumn 7, Issue 18, 2005, Pages 4033-4036

  Crimmins, Michael T ^a   McDougall, Patrick J ^a   Emmitte, Kyle A ^a  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BREVETOXIN A; ETHER DERIVATIVE; MARINE TOXIN; OXOCIN DERIVATIVE; POLYCYCLIC AROMATIC HYDROCARBON;

ALKYLATION; ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; CYCLIZATION; STEREOISOMERISM; SYNTHESIS;

ALKYLATION; CATALYSIS; CYCLIZATION; ETHERS, CYCLIC; MARINE TOXINS; MOLECULAR STRUCTURE; OXOCINS; POLYCYCLIC HYDROCARBONS, AROMATIC; STEREOISOMERISM;

EID: 24944494520     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol051543m     Document Type: Article

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