Abstract
2,2-Disubstituted cyclic 1,3-diketones containing a tethered electron-deficient alkene undergo chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations to give bridged bicyclic products in high enantioselectivities. Both bicyclo[3.2.1]octanes and bicyclo[3.3.1]nonanes are accessible using this methodology. This journal is
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APA
Burns, A. R., Madec, A. G. E., Low, D. W., Roy, I. D., & Lam, H. W. (2015). Enantioselective synthesis of bicyclo[3.n.1]alkanes by chiral phosphoric acid-catalyzed desymmetrizing Michael cyclizations. Chemical Science, 6(6), 3550–3555. https://doi.org/10.1039/c5sc00753d
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