Journal article

Transition metal-catalyzed intermolecular [5+2] and [5+2+1] cycloadditions of allenes and vinylcyclopropanes





Authors listWegner, HA; de Meijere, A; Wender, PA

Publication year2005

Pages6530-6531

JournalJournal of the American Chemical Society

Volume number127

Issue number18

ISSN0002-7863

DOI Linkhttps://doi.org/10.1021/ja043671w

PublisherAmerican Chemical Society


Abstract

Initial examples of the intermolecular Rh(I)-catalyzed [5+2] cycloaddition reaction of bifunctional allenes and vinylcyclopropanes are described. The reactions proceed with facility and in yields of up to 99% with a variety of alkyne-, ester-, styrene-, or cyano-substituents on the allene to afford the corresponding cycloadducts. In the presence of CO, the reaction proceeds to an eight-membered ring cycloadduct and its transannularly closed product, providing the first example of a three-component [5+2+1] cycloaddition with allenes.




Citation Styles

Harvard Citation styleWegner, H., de Meijere, A. and Wender, P. (2005) Transition metal-catalyzed intermolecular [5+2] and [5+2+1] cycloadditions of allenes and vinylcyclopropanes, Journal of the American Chemical Society, 127(18), pp. 6530-6531. https://doi.org/10.1021/ja043671w

APA Citation styleWegner, H., de Meijere, A., & Wender, P. (2005). Transition metal-catalyzed intermolecular [5+2] and [5+2+1] cycloadditions of allenes and vinylcyclopropanes. Journal of the American Chemical Society. 127(18), 6530-6531. https://doi.org/10.1021/ja043671w


Last updated on 2025-21-05 at 13:19