Issue 37, 2021

α-Hydroxy boron-enabled regioselective access to bifunctional halo-boryl alicyclic ethers and α-halo borons

Abstract

α-Hydroxy borons are an underutilized class of compounds and their only previous application involved oxidation into acylborons. Herein, we describe the synthesis of functionalized olefinic α-hydroxy borons and their utility to enable a novel and regioselective route to hitherto unknown bifunctional halo-boryl tetrahydrofurans/tetrahydropyrans and α-halo MIDA boronates. The orthogonally functionalized alicyclic ethers provided a building block-based approach for diversification of the tetrahydrofuran core.

Graphical abstract: α-Hydroxy boron-enabled regioselective access to bifunctional halo-boryl alicyclic ethers and α-halo borons

Supplementary files

Article information

Article type
Communication
Submitted
20 Jan 2021
Accepted
21 Mar 2021
First published
22 Mar 2021

Chem. Commun., 2021,57, 4564-4567

α-Hydroxy boron-enabled regioselective access to bifunctional halo-boryl alicyclic ethers and α-halo borons

L. Wang, S. Lin, Y. Zhu, D. Ferrante, T. Ishak, Y. Baba and A. Sharma, Chem. Commun., 2021, 57, 4564 DOI: 10.1039/D1CC00336D

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