Faustino, HélioAlonso García, IsaacMascareñas Cid, José LuisLópez García, Fernando2019-03-272019-03-272013Faustino, H. , Alonso, I. , Mascareñas, J. L. and López, F. (2013), Gold(I)‐Catalyzed Cascade Cycloadditions between Allenamides and Carbonyl‐Tethered Alkenes: An Enantioselective Approach to Oxa‐Bridged Medium‐Sized Carbocycles. Angew. Chem. Int. Ed., 52: 6526-6530. doi:10.1002/anie.2013027131433-7851http://hdl.handle.net/10347/18483This is the peer reviewed version of the following article: Faustino, H. , Alonso, I. , Mascareñas, J. L. and López, F. (2013), Gold(I)‐Catalyzed Cascade Cycloadditions between Allenamides and Carbonyl‐Tethered Alkenes: An Enantioselective Approach to Oxa‐Bridged Medium‐Sized Carbocycles. Angew. Chem. Int. Ed., 52: 6526-6530, which has been published in final form at https://doi.org/10.1002/anie.201302713. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived VersionsGold standard: Allenamides react with aldehydes or ketones having γ, δ, or ε alkenyl groups, upon activation with suitable gold catalysts, to provide oxa-bridged systems containing seven- to nine-membered carbocycles, in a formal cascade cycloaddition. By using chiral phosphoramidite/gold or bisphosphine/gold catalysts it is possible to obtain the oxa-bridged seven- and eight-membered rings with good to high enantioselectivityeng© 2013 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived VersionsAnnulationCascade reactionsHomogeneous catalysisEnantioselectiveGoldjournal article10.1002/anie.2013027131521-3773open access