Intermolecular [8+2] cycloaddition reactions of 2H-3-methoxycarbonylcyclohepta[b]furan-2-one with vinyl ethers: an approach to bicyclo[5.3.0]azulene derivatives.

TitleIntermolecular [8+2] cycloaddition reactions of 2H-3-methoxycarbonylcyclohepta[b]furan-2-one with vinyl ethers: an approach to bicyclo[5.3.0]azulene derivatives.
Publication TypeJournal Article
Year of Publication2002
AuthorsPham W, Weissleder R, Tung C-H
JournalTetrahedron Lett
Volume43
Issue1
Pagination19-20
Date Published2002 Jan 01
ISSN0040-4039
Abstract

Substituted bicyclo[5.3.0]azulene compounds are synthesized by intermolecular [8+2] cycloaddition reactions of lactone 1 with vinyl ethers-acetal decomposition products-are described. The reactions were found to be temperature and solvent dependent.

DOI10.1016/S0040-4039(01)02061-5
Alternate JournalTetrahedron Lett
PubMed ID20740048
PubMed Central IDPMC2926969
Grant ListR21 CA088365 / CA / NCI NIH HHS / United States
R21 CA088365-01 / CA / NCI NIH HHS / United States
R33 CA088365 / CA / NCI NIH HHS / United States
Related Institute: 
Molecular Imaging Innovations Institute (MI3)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065