Selective α-Me–C(sp <sup>3</sup> )–H borylation of methyl sulfides controlled by substrate–ligand electrostatic interaction

An iridium/bipyridine catalyzed selective α-Me–C(sp 3 )–H borylation of aryl methyl sulfides was developed. The high site-selectivity was achieved by an π–π stacking interaction between the substrate and an electron-deficient bipyridine ligand

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-01-01
DOI
https://doi.org/10.1039/d5qo00231a
Citations
3
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
2.81
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article

Selective α-Me–C(sp 3 )–H borylation of methyl sulfides controlled by substrate–ligand electrostatic interaction

Masahiro Higashi, Yoichiro Kuninobu, Shunsuke Yabu, Shogo Tobe et al.
3 citations
Organic Chemistry Frontiers
Catalytic C–H Functionalization Methods
2.81
article

Selective α-Me–C(sp 3 )–H borylation of methyl sulfides controlled by substrate–ligand electrostatic interaction

Masahiro Higashi, Yoichiro Kuninobu, Shunsuke Yabu, Shogo Tobe, Hirofumi Sato, Jinping Li, Rui-Mu Yu
article en
3 citations

Abstract

An iridium/bipyridine catalyzed selective α-Me–C(sp 3 )–H borylation of aryl methyl sulfides was developed. The high site-selectivity was achieved by an π–π stacking interaction between the substrate and an electron-deficient bipyridine ligand

Organic Chemistry FrontiersVol. 12(19)
Kyushu University (JP), Guangxi University (CN), Kyoto University (JP), Guangxi Academy of Sciences (CN), Nagoya University (JP)
Openalex Percentile: Top 11%
Catalytic C–H Functionalization Methods
2.81
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