Mechanistic Investigations of Chiral Lithium Binaphtholate Catalysis for Asymmetric Aldol–Tishchenko Reaction of α-Fluoroarylketones
In this study, we analyzed the asymmetric aldol-Tishchenko reaction of α-fluoroarylketones with aldehydes in the presence of chiral lithium binaphtholate, which was readily prepared from a chiral BINOL derivative and lithium <i>tert</i>-butoxide. This tandem reaction afforded enantiomerically enriched 2-fluoro-1,3-diols with three contiguous stereogenic centers in high yield and with high diastereo- and enantioselectivities. Moreover, mechanistic investigations of the lithium binaphtholate-catalyzed enantioselective aldol-Tishchenko reaction were performed based on the kinetic isotope effect and computational analyses.
Authors
- Shunsuke Kotani (ORCID: https://orcid.org/0000-0003-4801-8341)
- Makoto Nakajima (ORCID: https://orcid.org/0000-0003-3547-1307)
- Sachie Arae
- Masaharu Sugiura (ORCID: https://orcid.org/0000-0002-7173-4568)
- Toshifumi Asano
Institutions
- Sojo University (JP)
- Kumamoto University (JP)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2024-11-08
- DOI
- https://doi.org/10.1021/acs.joc.4c01404
- Citations
- 1
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.21
Funders
- Japan Society for the Promotion of Science