Journal of the American Chemical Society · 2018 · 156 citations · 88 references
We report a method for the highly enantioselective CuH-catalyzed allylation of ketones that employs terminal allenes as allylmetal surrogates. Ketones and allenes bearing diverse and sensitive functional groups are efficiently coupled with high stereoselectivity and exclusive branched regioselectivity. In stoichiometric experiments, each elementary step of the proposed hydrocupration-addition-metathesis mechanism can be followed by NMR spectroscopy.
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Catalytic asymmetric hydroamination of unactivated internal olefins to aliphatic amines
Yang Yang, Shi‐Liang Shi, Dawen Niu et al. · Science · 2015 · 385 citations · Full text
Yuya Miki, Koji Hirano, Tetsuya Satoh et al. · Angewandte Chemie International Edition · 2013 · 362 citations
Chemical Engineering, Enantioselective Synthesis, Hydroxylamine Derivatives +12
Solvias Josiphos Ligands: From Discovery to Technical Applications
Hans‐Ulrich Blaser, Walter Brieden, Benoı̂t Pugin et al. · Topics in Catalysis · 2002 · 327 citations