Non-Ionic Peterson-Type Olefination Reactivity and its Use in a Silicon-Promoted Carbonyl-Carbonyl Cross Coupling Reaction.

Autor: Tran TT; Department of Chemistry-Ångström Laboratory, Uppsala University, Box 523, 751 20, Uppsala., Arkhypchuk AI; Department of Chemistry-Ångström Laboratory, Uppsala University, Box 523, 751 20, Uppsala., Ott S; Department of Chemistry-Ångström Laboratory, Uppsala University, Box 523, 751 20, Uppsala.
Jazyk: angličtina
Zdroj: Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2024 Aug 26, pp. e202411265. Date of Electronic Publication: 2024 Aug 26.
DOI: 10.1002/anie.202411265
Abstrakt: 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 SiO 2 , 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.
(© 2024 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.)
Databáze: MEDLINE
Externí odkaz: