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β-羟基烷基膦硫化物中[1,3]/[1,4]-硫原子迁移

[1,3]/[1,4]-Sulfur atom migration in β-hydroxyalkylphosphine sulfides.

作者信息

Włodarczyk Katarzyna, Borowski Piotr, Stankevič Marek

机构信息

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.

出版信息

Beilstein J Org Chem. 2020 Jan 21;16:88-105. doi: 10.3762/bjoc.16.11. eCollection 2020.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49ee/7006489/872e70c86233/Beilstein_J_Org_Chem-16-88-g004.jpg

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