首页|Nickel-Catalyzed Regioselective Hydrosilylation of Conjugated Dienest

Nickel-Catalyzed Regioselective Hydrosilylation of Conjugated Dienest

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With the increasing demand for homoallylic silanes and allylic silanes,the highly efficient and regioselective hydrosilylations of conju-gated dienes are urgently needed.Herein,we developed a Ni-catalyzed regiodivergent hydrosilylation of aromatic conjugated dienes by adjusting the temperature and ligands.Under low temperature(-30 ℃),an eternal-ligand-free system(Ni/t-BuOK)can efficiently facilitate the 3,4-anti-Markovnikov hydrosilylation to provide homoallylic silanes via electrophilic activation process;under room temperature(25 ℃),a ligand-controlled system(Ni/t-BuOK/PPh3)can eventuate the 3,4-Markovnikov hydrosilylation to produce allylic silanes via Chalk-Harrod process.Both systems are compatible with various conjugated dienes and primary silanes in excellent yields and regioselectivities.

Nickel-catalyzedRegioselective hydrosilylationConjugated dienesElectrophilic activationHomoallylic silanes

Xiaoyu Wu、Wei Liu、Liqun Yang、Yue Wang、Tianwen Liu、Yao Yuan、Yan Lu、Zhaoguo Zhang

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Shanghai Key Laboratory for Molecular Engineering of Chiral Drugs,School of Chemistry and Chemical Engineering,Shanghai Jiao Tong University,800 Dongchuan Road,Shanghai 200240,China

Joseph Black Building,The University of Edinburgh,David Brewster Road,Edinburgh,EH9 3FJ,UK

国家自然科学基金

2024

中国化学(英文版)
中国化学会 上海有机化学研究所

中国化学(英文版)

CSTPCD
影响因子:0.848
ISSN:1001-604X
年,卷(期):2024.42(1)
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