Metal-free C(sp<sup>3</sup>)–Si activation enables regiocontrolled [4 + 2] cycloaddition to benzosilacycloethers

A transition-metal-free strategy enables inverse site-selective [4 + 2] cycloaddition of benzosilacyclobutanes with activated ketones via DMSO-mediated C(sp 3 )–Si bond cleavage, contrasting conventional transition-metal-catalyzed pathways.

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Publication Details

Journal
Green Chemistry
Published
2025-01-01
DOI
https://doi.org/10.1039/d5gc03044g
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Metal-free C(sp3)–Si activation enables regiocontrolled [4 + 2] cycloaddition to benzosilacycloethers

Yan Sun, Liuzhou Gao, Shenglong Wang, Ying Han et al.
Green Chemistry
Catalytic Alkyne Reactions
article

Metal-free C(sp3)–Si activation enables regiocontrolled [4 + 2] cycloaddition to benzosilacycloethers

Yan Sun, Liuzhou Gao, Shenglong Wang, Ying Han, Yan Ping Sun, Yidong Wang, Zhenxing Li, Jingyi Hu, Yanxuan Wen
article en

Abstract

A transition-metal-free strategy enables inverse site-selective [4 + 2] cycloaddition of benzosilacyclobutanes with activated ketones via DMSO-mediated C(sp 3 )–Si bond cleavage, contrasting conventional transition-metal-catalyzed pathways.

Green ChemistryVol. 27(34)
Yangzhou University (CN), Nanjing University (CN)
Openalex Percentile: Top 85%
Catalytic Alkyne Reactions
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