Synthesis of Dibenzosiloles via Pyridine/Zn System-Enabled Cross-Couplings of Diiodidobiaryls with Dihalosilanes

-butylpyridine additive. Compared with conventional lithiation-silylation or transition-metal-catalyzed approaches, this new protocol is operationally simple, economical, and exhibits a broad substrate scope with scalability. It thus provides a versatile and general platform for accessing diverse silafluorene architectures.

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Publication Details

Journal
Organic Letters
Published
2026-04-01
DOI
https://doi.org/10.1021/acs.orglett.6c01069
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of Dibenzosiloles via Pyridine/Zn System-Enabled Cross-Couplings of Diiodidobiaryls with Dihalosilanes

Weilong Xie, Qinying Zhao, Xiaofu Jian, Xibao Zhang
Organic Letters
Catalytic Cross-Coupling Reactions
article

Synthesis of Dibenzosiloles via Pyridine/Zn System-Enabled Cross-Couplings of Diiodidobiaryls with Dihalosilanes

Weilong Xie, Qinying Zhao, Xiaofu Jian, Xibao Zhang
article en

Abstract

-butylpyridine additive. Compared with conventional lithiation-silylation or transition-metal-catalyzed approaches, this new protocol is operationally simple, economical, and exhibits a broad substrate scope with scalability. It thus provides a versatile and general platform for accessing diverse silafluorene architectures.

Organic LettersVol. 28(14)
Donghua University (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Industry, innovation and infrastructure
Openalex Percentile: Top 34%
Catalytic Cross-Coupling Reactions
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Synthesis of Dibenzosiloles via Pyridine/Zn System-Enabled Cross-Couplings of Diiodidobiaryls with Dihalosilanes — Weilong Xie, Qinying Zhao, et al. · Organic Letters (2026) | TGRS Research Map | TGRS