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有催化剂和无催化剂的氧硼化反应:通过B-O σ键加成生成硼化异恶唑。

Oxyboration with and without a Catalyst: Borylated Isoxazoles via B-O σ-Bond Addition.

作者信息

Tu Kim N, Hirner Joshua J, Blum Suzanne A

机构信息

Department of Chemistry, University of California-Irvine , Irvine, California 92697-2025, United States.

出版信息

Org Lett. 2016 Feb 5;18(3):480-3. doi: 10.1021/acs.orglett.5b03530. Epub 2016 Jan 15.

Abstract

Herein we report an oxyboration reaction with activated substrates that employs B-O σ bond additions to C-C π bonds to form borylated isoxazoles, which are potential building blocks for drug discovery. Although this reaction can be effectively catalyzed by gold, it is the first example of uncatalyzed oxyboration of C-C π bonds by B-O σ bonds--and only the second example that is catalyzed. This oxyboration reaction is tolerant of groups incompatible with alternative lithiation/borylation and palladium-catalyzed C-H activation/borylation technologies for the synthesis of borylated isoxazoles.

摘要

在此,我们报道了一种与活化底物发生的氧硼化反应,该反应利用B-O σ键加成到C-C π键上以形成硼化异恶唑,它们是药物发现的潜在构建模块。尽管该反应可被金有效催化,但这是B-O σ键对C-C π键进行无催化氧硼化的首个实例——且仅是被催化的第二个实例。这种氧硼化反应能够耐受与用于合成硼化异恶唑的替代锂化/硼化以及钯催化的C-H活化/硼化技术不相容的基团。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f91/4763986/2fd067413be1/ol-2015-03530p_0003.jpg

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