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Updated: Apr 18, 2026

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
Asymmetric conjugate additions and allylic alkylations using nucleophiles generated by hydro- or carbometallation
Rebecca M Maksymowicz1, Andrew J Bissette, Stephen P Fletcher
1Chemistry Research Laboratory, Department of Chemistry, University of Oxford, 12 Mansfield Rd., Oxford, OX1 3TA (UK).
Abstract:
This Minireview discusses catalytic asymmetric conjugate addition and allylic alkylation reactions where the nucleophiles were generated in situ by hydrometallation or carbometallation. This exciting recent trend in asymmetric catalysis promises to expand the range of transformations available for the rapid and selective assembly of complex, functional molecules for both academic and industrial research. This Minireview aims to serve as a reference for studies reported to date and discusses the current state-of-the-art, scope and limitations of these processes.
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