Rhodium-catalyzed [5+2] cycloadditions of allenes and vinylcyclopropanes: Asymmetric total synthesis of (+)-dictamnol

Citation
Pa. Wender et al., Rhodium-catalyzed [5+2] cycloadditions of allenes and vinylcyclopropanes: Asymmetric total synthesis of (+)-dictamnol, ORG LETT, 1(1), 1999, pp. 137-139
Citations number
35
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANIC LETTERS
ISSN journal
15237060 → ACNP
Volume
1
Issue
1
Year of publication
1999
Pages
137 - 139
Database
ISI
SICI code
1523-7060(19990715)1:1<137:R[COAA>2.0.ZU;2-Q
Abstract
[GRAPHICS] The asymmetric synthesis of (+)-dictamnol is described, based on the rhodiu m catalyzed [5 + 2] cycloaddition of an allene and vinylcyclopropane. This cycloaddition methodology provides the basis for a general and efficient ro ute to various bicyclo[5.3.0]decenes, ring systems common to a wide range o f natural and designed compounds of structural and medicinal interest.