Włodarczyk Katarzyna, Borowski Piotr, Stankevič Marek
Department of Organic Chemistry, Faculty of Chemistry, Marie Curie-Skłodowska University in Lublin, 33 Gliniana St., 20-614 Lublin, Poland.
Department of Chromatographic Methods, Faculty of Chemistry, Marie Curie-Skłodowska University in Lublin, 3 Marie Curie-Skłodowska Sq., 20-031 Lublin, Poland.
Beilstein J Org Chem. 2020 Jan 21;16:88-105. doi: 10.3762/bjoc.16.11. eCollection 2020.
β-Hydroxyalkylphosphine sulfides undergo [1,3]- or [1,4]-sulfur atom phosphorus-to-carbon migration in the presence of Lewis or Brønsted acids. The direction of sulfur atom migration depends on the type of acid used for the reaction. In the presence of a Brønsted acid, mainly [1,3]-rearrangement is observed, whereas a Lewis acid catalyzes the [1,4]-sulfur migration. To gain insight into the mechanism of these transformations, the stereochemistry of these rearrangements have been tested, along with the conduction of some control experiments and DFT calculations.
β-羟烷基膦硫化物在路易斯酸或布朗斯特酸存在下会发生[1,3]-或[1,4]-硫原子从磷到碳的迁移。硫原子迁移的方向取决于用于该反应的酸的类型。在布朗斯特酸存在下,主要观察到[1,3]-重排,而路易斯酸催化[1,4]-硫迁移。为了深入了解这些转化的机理,已经测试了这些重排的立体化学,并进行了一些对照实验和密度泛函理论计算。