环加成
化学
羰基
反应性(心理学)
醛
偶联反应
离子键合
烯烃
药物化学
光化学
有机化学
催化作用
医学
离子
替代医学
病理
作者
Thuan Thi Tran,Anna I. Arkhypchuk,Sascha Ott
标识
DOI:10.1002/anie.202411265
摘要
The [2+2] cycloaddition reaction between the Si=C double bond of adamantylsilene and the carbonyl group of aliphatic, aromatic or acetylenic ketones and aldehydes is demonstrated. The product of this reaction that is central to a non-ionic version of the Peterson olefination is an unusual four-membered 1,2-silaoxetane heterocycle that was characterized spectroscopically and crystallographically. In the presence of SiO2, the silaoxetane undergoes retro-cycloaddition with the formation of alkene products. As the [2+2] cycloaddition proceeds without the necessity of any base, enolizable ketones can be converted into olefins. In addition, it is shown that the adamantylsilene can be produced in situ by a sila-Peterson reaction, providing valuable input for the development of a new one-pot silicon-based reductive carbonyl-carbonyl cross coupling methodology.
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