Synthesis of an enantiomerically pure 2,2,4-trisubstituted cyclobutanone building block by zirconocene-promoted deoxygenative ring contraction of structurally modified 4-vinylfuranosides

Tetrahedron

Volumn 60, Issue 6, 2004, Pages 1353-1358

  Paquette, Leo A ^a   Kang, Ho Jung ^a,b  

^a OHIO STATE UNIVERSITY   (United States)

^b Kyung Hee University   (South Korea)

Author keywords

Cyclobutanes; D Glucose; Diastereoselectivity; Ring contraction; Zirconocene

Indexed keywords

2,2,4 CYCLOBUTANONE; CYCLOBUTANONE DERIVATIVE; FURAN DERIVATIVE; GLUCOSE; UNCLASSIFIED DRUG; VINYL DERIVATIVE; ZIRCONOCENE;

ARTICLE; CHEMICAL BOND; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; DEOXYGENATION; ENANTIOMER; NUCLEAR MAGNETIC RESONANCE; NUCLEAR OVERHAUSER EFFECT; PRIORITY JOURNAL; SYNTHESIS;

EID: 1642431607     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.07.012     Document Type: Article

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