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Updated: May 16, 2025

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
Conjugate Addition of Chiral Allenylcopper Species to Vinyl Bis(sulfone) To Access an All-Carbon Quaternary Center
Wan Seok Yoon1, Jaehyun You2, Jieun You1
1Department of Chemistry, Sungkyunkwan University, Suwon 16419, Korea.
Abstract:
Asymmetric formation of all-carbon quaternary centers has been recognized as a challenging area in organic synthesis. Herein, we report a copper-catalyzed approach toward coupling of two alkenyl substrates, resulting in the formation of a chiral all-carbon quaternary center. In the reaction, axially chiral tetrasubstituted allenylcopper species were generated catalytically and chemoselectively, in situ from the substituted enynes, and remarkably performed as an efficient organometallic nucleophile in conjugate addition to unsaturated sulfones.
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