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. Author manuscript; available in PMC: 2018 Dec 22.
Published in final edited form as: Angew Chem Int Ed Engl. 2017 Dec 4;56(52):16631–16635. doi: 10.1002/anie.201708784

Scheme 2.

Scheme 2

Enantioselective reductive allylation of β-methyl enals.[a] [a] All reactions were run on 0.4 mmol scale. Yields of isolated products are given. The e.r. values were determined by HPLC analysis using chiral stationary phases. [b] Reaction was run at 1 M concentration. [c] 5 equivalents of t-BuOH were used in the absence of toluene. The (Z)-silyl enal 3g was used in the reaction. See Supplementary Information for experimental details and stereochemical proof.