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Updated: Sep 22, 2025

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
Organocatalytic Enantioselective α-Bromination of Aldehydes with N-Bromosuccinimide
George Hutchinson1, Carla Alamillo-Ferrer1, Martín Fernández-Pascual1
1The University of Manchester, Department of Chemistry, Oxford Road, M13 9PL Manchester, U.K.
Abstract:
Despite the wealth of existing organocatalytic, enantioselective transformations, the α-bromination of aldehydes remains a challenging reaction. The four examples reported to date require expensive, inconvenient brominating agents to achieve the desired products in excellent yields and enantioselectivities. The preferred brominating agent, N-bromosuccinimide (NBS), has been repeatedly discarded for these reactions because it results in low yields and relatively poor enantioselectivities. We describe a methodology that uses NBS and performs excellently with low catalyst loadings, short reaction times, and mild temperatures.
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