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.

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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

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article

Synthesis of ketones and mono-fluoro ketones via boron enolates formed by substitution of esters with benzylboronic esters

Josephine Stewart, Graham Pattison, Pankaj Kumar, Leah Mistry
Chemical Communications
Fluorine in Organic Chemistry
article

Synthesis of ketones and mono-fluoro ketones via boron enolates formed by substitution of esters with benzylboronic esters

Josephine Stewart, Graham Pattison, Pankaj Kumar, Leah Mistry
article en

Abstract

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.

Chemical CommunicationsVol. 62(1)
University of St Andrews (GB), University of Lincoln (GB)
Engineering and Physical Sciences Research Council
Openalex Percentile: Top 70%
Fluorine in Organic Chemistry
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