Traceless Silicon-Tether Strategy for the Synthesis of a Tetraphenylammonium Salt

. DFT calculations suggest β-silicon stabilization in the cyclization transition state, although competing pathways are kinetically favored. This work highlights the potential of intramolecular designs for accessing sterically hindered organic cations.

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Publication Details

Journal
Organic Letters
Published
2026-04-01
DOI
https://doi.org/10.1021/acs.orglett.6c00906
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Traceless Silicon-Tether Strategy for the Synthesis of a Tetraphenylammonium Salt

Munetaka Kunishima, Hikaru Fujita, Shiori Kobayashi, Yuria Sato
Organic Letters
Organoboron and organosilicon chemistry
article

Traceless Silicon-Tether Strategy for the Synthesis of a Tetraphenylammonium Salt

Munetaka Kunishima, Hikaru Fujita, Shiori Kobayashi, Yuria Sato
article en

Abstract

. DFT calculations suggest β-silicon stabilization in the cyclization transition state, although competing pathways are kinetically favored. This work highlights the potential of intramolecular designs for accessing sterically hindered organic cations.

Organic LettersVol. 28(15)
Kanazawa University (JP), Kobe Gakuin University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 30%
Organoboron and organosilicon chemistry
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