A Building Block Strategy for Construction of C(sp <sup>3</sup> )–SCF <sub>3</sub> Bonds via Nickel-Catalyzed 1,2-Difunctionalization of Trifluoromethylthiolated Alkenes

The trifluoromethylthiol (SCF 3 ) group has emerged as a valuable motif in medicinal chemistry owing to its strong electron-withdrawing nature and its high lipophilicity. Despite significant advances in SCF 3 incorporation into a variety of molecules, the construction of C(sp 3 )–SCF 3 bonds remains a notable challenge. Herein, we present a Ni-catalyzed 1,2-difunctionalization using a newly designed SCF 3 -containing synthon readily accessible in a single step.

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Publication Details

Journal
Organic Letters
Published
2026-07-22
DOI
https://doi.org/10.1021/acs.orglett.6c02895
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
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article

A Building Block Strategy for Construction of C(sp 3 )–SCF 3 Bonds via Nickel-Catalyzed 1,2-Difunctionalization of Trifluoromethylthiolated Alkenes

Olivier Riant, Xavier Vanderbiest
Organic Letters
Fluorine in Organic Chemistry
article

A Building Block Strategy for Construction of C(sp 3 )–SCF 3 Bonds via Nickel-Catalyzed 1,2-Difunctionalization of Trifluoromethylthiolated Alkenes

Olivier Riant, Xavier Vanderbiest
article en

Abstract

The trifluoromethylthiol (SCF 3 ) group has emerged as a valuable motif in medicinal chemistry owing to its strong electron-withdrawing nature and its high lipophilicity. Despite significant advances in SCF 3 incorporation into a variety of molecules, the construction of C(sp 3 )–SCF 3 bonds remains a notable challenge. Herein, we present a Ni-catalyzed 1,2-difunctionalization using a newly designed SCF 3 -containing synthon readily accessible in a single step.

Organic Letters
UCLouvain (BE)
Sustainable cities and communities
Openalex Percentile: Top 9%
Fluorine in Organic Chemistry
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