Direct Diastereo- and Enantioselective Vinylogous Michael Additions of Linear Enones

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Abstract

A direct vinylogous Michael addition using linear vinylogous Michael donors has been developed. Notably, even γ-substituted Michael donors cleanly afforded γ-alkylated products in high yield and ee by this method. Moreover, control experiments revealed that, for these and related linear vinylogous Michael donors, the size of the Michael acceptor strongly influences whether α- or γ-alkylation occurs, not simply blocking effects of cocatalysts as suggested previously.

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Guo, Q., Fraboni, A. J., & Brenner-Moyer, S. E. (2016, June 3). Direct Diastereo- and Enantioselective Vinylogous Michael Additions of Linear Enones. Organic Letters. American Chemical Society. https://doi.org/10.1021/acs.orglett.6b01050

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