Catalytic Asymmetric Carbosilylation of Methyl Propiolate with Bis-silyl Ketene Acetals
We report a catalytic asymmetric silylative α-alkenylation of bis-silyl ketene acetals (bis-SKAs) with methyl propiolate via conjugate addition. In contrast to prior Brønsted-base activation of C-H acidic nucleophiles (β-ketoesters and oxazolones), electrophilic activation of the alkynoate through silylium-asymmetric counteranion-directed catalysis (Si-ACDC) enables this transformation. DFT studies support a pathway in which silylium-mediated addition forms a substituted alkoxy(trimethylsilyloxy)propadiene (silyl propadienone acetal, SPA) that rapidly isomerizes via C-silylation accompanied by an O-desilylation to the α,β-unsaturated α-silyl ester with high stereocontrol. The reaction shows a broad scope with uniformly excellent enantio- and diastereoselectivities, and we demonstrate several downstream modifications of the products.
Authors
- Benjamin Mitschke (ORCID: https://orcid.org/0000-0002-2942-2448)
- Benjamin List
- Chendan Zhu
Institutions
- Max-Planck-Institut für Kohlenforschung (DE)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-12-22
- DOI
- https://doi.org/10.1021/jacs.5c17310
- Citations
- 1
- Primary Topic
- Organoboron and organosilicon chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.94