化学
硅烷化
硅烷
钴
催化作用
亲核细胞
产量(工程)
钳子运动
有机化学
商品化学品
组合化学
小学(天文学)
硅烷
物理
冶金
材料科学
天文
作者
Ewelina Szafoni,Krzysztof Kuciński,Grzegorz Hreczycho
标识
DOI:10.1080/17518253.2022.2133554
摘要
Various commercially available primary and secondary hydrosilanes were exploited for versatile direct dehydrocoupling with alcohols and phenols through cobalt catalysis. The protocol enables efficient Si–O bond formation with a host of O–nucleophiles and silanes (27 examples, 67–91% yield), with precatalyst loadings of 0.5–2 mol%. Beyond enabling a practical and greener approach to silyl ethers, this type of pincer-supported cobalt catalysis provides a blueprint for the development of a broad range of efficient reactions leading to synthetically relevant organometalloids. Moreover, the use of silanes as substrates and precatalyst activators permits the use of inexpensive and easily accessible Earth-abundant metal complexes and avoids the presence of additional activators.
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