Highly functionalized donor–acceptor cyclopropanes applied toward the synthesis of the Melodinus alkaloids

[Display omitted] A series of highly substituted vinylcyclopropanes were prepared and examined as reaction partners in a palladium-catalyzed (3+2) cycloaddition with nitrostyrenes. Described herein are our efforts to synthesize an elusive 1,1-divinylcyclopropane by several distinct approaches, and t...

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Veröffentlicht in:Tetrahedron letters 2015-06, Vol.56 (23), p.2983-2990
Hauptverfasser: Goldberg, Alexander F.G., Craig, Robert A., O’Connor, Nicholas R., Stoltz, Brian M.
Format: Artikel
Sprache:eng
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Zusammenfassung:[Display omitted] A series of highly substituted vinylcyclopropanes were prepared and examined as reaction partners in a palladium-catalyzed (3+2) cycloaddition with nitrostyrenes. Described herein are our efforts to synthesize an elusive 1,1-divinylcyclopropane by several distinct approaches, and to apply surrogates of this fragment toward the synthesis of the Melodinus alkaloids.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2014.09.016