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Updated: Dec 27, 2025

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
Nucleophilic Addition of Benzylboronates to Activated Ketones
Jacob C Hayes1, Michael R Hollerbach1, Timothy J Barker1
1Department of Chemistry and Biochemistry, College of Charleston, Charleston, SC 29424.
Abstract:
A method has been developed for the addition of benzylboronic acid pinacol ester to activated ketones including trifluoromethyl ketones in good yields. The use of DABCO as an additive was found to enhance the rate and efficiency of this reaction. In reactions of ketones with a second carbonyl group present such as an ester or amide, good chemoselectivity for the ketone was observed. Competition experiments suggest an electrophile relative reactivity order of CF2H ketone > CF3 ketone > aldehyde under these reaction conditions.
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