Directed Secondary C(sp<sup>3</sup>)–H Borylation by a Phenoxyimine Iridium Catalyst at Room Temperature

Here, we report that directed secondary C(sp<sup>3</sup>)-H borylation at room temperature was achieved by using phenoxyimine iridium complexes as catalysts. This reaction enables the introduction of a boryl group at the β position of a directing group, such as a pyridyl and pyrazolyl groups. Furthermore, it was indicated that the addition of a small amount of pinacolborane is important for the efficient generation of catalytically active species.

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Publication Details

Journal
Organic Letters
Published
2025-09-01
DOI
https://doi.org/10.1021/acs.orglett.5c03128
Citations
1
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
0.94

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article

Directed Secondary C(sp3)–H Borylation by a Phenoxyimine Iridium Catalyst at Room Temperature

Fumitoshi Kakiuchi, Takuya Kochi, Ryosuke Ueda
1 citations
Organic Letters
Catalytic C–H Functionalization Methods
0.94
article

Directed Secondary C(sp3)–H Borylation by a Phenoxyimine Iridium Catalyst at Room Temperature

Fumitoshi Kakiuchi, Takuya Kochi, Ryosuke Ueda
article en
1 citations

Abstract

Here, we report that directed secondary C(sp<sup>3</sup>)-H borylation at room temperature was achieved by using phenoxyimine iridium complexes as catalysts. This reaction enables the introduction of a boryl group at the β position of a directing group, such as a pyridyl and pyrazolyl groups. Furthermore, it was indicated that the addition of a small amount of pinacolborane is important for the efficient generation of catalytically active species.

Organic LettersVol. 27(36)
Keio University (JP)
Core Research for Evolutional Science and Technology
Openalex Percentile: Top 22%
Catalytic C–H Functionalization Methods
0.94
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