Add time:07/27/2019         Source:sciencedirect.com

An asymmetric Michael addition of diphenylphosphine to β,γ-unsaturated α-keto esters was developed using a P-stereogenic pincer-Pd complex as a catalyst. The corresponding hydrophosphination products were obtained in good yields (up to 94%) and with moderate to good enantioselectivities (up to 93% ee) under the optimum reaction conditions.

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