Selective Synthesis of α,α-Difluoro- and α-Monofluoro Methylene Substituted Arenes by Defluoro C–C Bond Coupling

A mild and site-selective method for synthesizing α,α-difluoro- and α-monofluoro benzylic compounds by defluoro/C-C coupling reactions is presented. The process utilizes readily available aryl-CF<sub>3</sub> and -CF<sub>2</sub>R substrates as building blocks, along with organodiboron reagents and a Lewis base activator. This methodology efficiently produces benzylic fluoroarenes with adjacent quaternary or tertiary carbons in high yields and with excellent site selectivity. The resulting products feature an alkenyl boronic ester, providing a versatile handle for subsequent synthetic modifications.

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Publication Details

Journal
Organic Letters
Published
2025-10-17
DOI
https://doi.org/10.1021/acs.orglett.5c03667
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Selective Synthesis of α,α-Difluoro- and α-Monofluoro Methylene Substituted Arenes by Defluoro C–C Bond Coupling

Simon J. Meek, Hawa Keita, José L. Rosario‐Collazo, Mario Velo
Organic Letters
Fluorine in Organic Chemistry
article

Selective Synthesis of α,α-Difluoro- and α-Monofluoro Methylene Substituted Arenes by Defluoro C–C Bond Coupling

Simon J. Meek, Hawa Keita, José L. Rosario‐Collazo, Mario Velo
article en

Abstract

A mild and site-selective method for synthesizing α,α-difluoro- and α-monofluoro benzylic compounds by defluoro/C-C coupling reactions is presented. The process utilizes readily available aryl-CF<sub>3</sub> and -CF<sub>2</sub>R substrates as building blocks, along with organodiboron reagents and a Lewis base activator. This methodology efficiently produces benzylic fluoroarenes with adjacent quaternary or tertiary carbons in high yields and with excellent site selectivity. The resulting products feature an alkenyl boronic ester, providing a versatile handle for subsequent synthetic modifications.

Organic LettersVol. 27(43)
University of North Carolina at Chapel Hill (US)
Openalex Percentile: Top 77%
Fluorine in Organic Chemistry
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