Synthesis of ketones and mono-fluoro ketones <i>via</i> boron enolates formed by substitution of esters with benzylboronic esters
Benzylboronic esters can be deprotonated using LiTMP and engaged in useful C-C bond-forming processes. Here we report that they undergo acylation with esters. We also report a fluorinative coupling reaction performed through nucleophilic substitution of a lithiated benzylboronic ester with an ester, and trapping of the resultant boron enolate with the fluorinating agent NFSI.
Authors
- Josephine Stewart
- Graham Pattison (ORCID: https://orcid.org/0000-0003-0116-8457)
- Pankaj Kumar (ORCID: https://orcid.org/0000-0002-7000-5099)
- Leah Mistry
Institutions
- University of St Andrews (GB)
- University of Lincoln (GB)
Publication Details
- Journal
- Chemical Communications
- Published
- 2025-11-25
- DOI
- https://doi.org/10.1039/d5cc05350a
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Engineering and Physical Sciences Research Council