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Regioselective silyl installation for arene diversification

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Regioselective silyl installation for arene diversification. / Docherty, Jamie.
In: Nature Catalysis, Vol. 8, 25.04.2025, p. 291-292.

Research output: Contribution to Journal/MagazineComment/debate

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Docherty J. Regioselective silyl installation for arene diversification. Nature Catalysis. 2025 Apr 25;8:291-292. doi: 10.1038/s41929-025-01314-9

Author

Docherty, Jamie. / Regioselective silyl installation for arene diversification. In: Nature Catalysis. 2025 ; Vol. 8. pp. 291-292.

Bibtex

@article{52f87ffa1f794e7bbfae80236d607c9c,
title = "Regioselective silyl installation for arene diversification",
abstract = "Using a single ruthenium catalyst, site-selective C–H functionalization methods are developed for the installation of silylmethyl synthetic handles at either ortho or meta positions on diverse arenes, enabling a wide range of downstream transformations. Mechanistic studies highlight that biscyclometallated ruthenium(II) species are key to this reactivity, offering insight for future developments.",
author = "Jamie Docherty",
year = "2025",
month = apr,
day = "25",
doi = "10.1038/s41929-025-01314-9",
language = "English",
volume = "8",
pages = "291--292",
journal = "Nature Catalysis",
publisher = "Springer Nature",

}

RIS

TY - JOUR

T1 - Regioselective silyl installation for arene diversification

AU - Docherty, Jamie

PY - 2025/4/25

Y1 - 2025/4/25

N2 - Using a single ruthenium catalyst, site-selective C–H functionalization methods are developed for the installation of silylmethyl synthetic handles at either ortho or meta positions on diverse arenes, enabling a wide range of downstream transformations. Mechanistic studies highlight that biscyclometallated ruthenium(II) species are key to this reactivity, offering insight for future developments.

AB - Using a single ruthenium catalyst, site-selective C–H functionalization methods are developed for the installation of silylmethyl synthetic handles at either ortho or meta positions on diverse arenes, enabling a wide range of downstream transformations. Mechanistic studies highlight that biscyclometallated ruthenium(II) species are key to this reactivity, offering insight for future developments.

U2 - 10.1038/s41929-025-01314-9

DO - 10.1038/s41929-025-01314-9

M3 - Comment/debate

VL - 8

SP - 291

EP - 292

JO - Nature Catalysis

JF - Nature Catalysis

ER -