SmI <sub>2</sub> ‐Catalyzed Coupling of Alkyl Housane Ketones and Alkenes in an Approach to Norbornanes
Abstract
Abstract Cross‐coupling strategies involving strain release have gained significant recent attention for the construction of complex molecular frameworks, particularly in the context of preparing bioisosteres for medicinal chemistry. While the reactivity of cyclopropanes and bicyclo[1.1.0]butanes (BCBs) has been extensively studied, higher homologues are emerging as valuable substrates for synthesis. For example, methods for the fragmentation and coupling of bicyclo[2.1.0]pentane, or housane, ketones show promise but are currently limited in substrate scope. Here, we describe a mild, atom‐economical, samarium diiodide (Sml 2 )‐catalyzed fragmentation and coupling of alkyl and aryl housane ketones with alkenes that grants access to functionalized norbornane structural motifs, not easily accessible by classical cycloaddition approaches, and with considerable potential for further manipulation.
Article Details
Authors (8)
Debayan Roy
Department of Chemistry University of Manchester Oxford Road Manchester M13 9PL UK
Jack I. Mansell
Department of Chemistry University of Manchester Oxford Road Manchester M13 9PL UK
Giorgia Barison
Department of Chemistry University of Manchester Oxford Road Manchester M13 9PL UK
Song Yu
College of Life Sciences
Rocco Katavic
Department of Chemistry University of Manchester Oxford Road Manchester M13 9PL UK
Ciro Romano
Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom
Nikolas Kaltsoyannis
Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, U.K.
David J. Procter
Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom