Issue 16, 2021

Chemoselective hydroborative reduction of nitro motifs using a transition-metal-free catalyst

Abstract

The chemoselective catalytic reduction of nitro scaffolds to value-added amine functions is desirable but challenging. We developed a combined KOtBu/BEt3 catalyst for deoxygenative reduction of nitroarenes, nitro heteroarenes and even notoriously challenging nitroalkanes using pinacolborane under mild reaction conditions. The novel transition-metal-free strategy is readily applicable to the preparation of commercially available pharmaceuticals.

Graphical abstract: Chemoselective hydroborative reduction of nitro motifs using a transition-metal-free catalyst

Supplementary files

Article information

Article type
Research Article
Submitted
06 May 2021
Accepted
08 Jun 2021
First published
15 Jun 2021

Org. Chem. Front., 2021,8, 4554-4559

Chemoselective hydroborative reduction of nitro motifs using a transition-metal-free catalyst

W. Yao, J. Wang, Y. Lou, H. Wu, X. Qi, J. Yang and A. Zhong, Org. Chem. Front., 2021, 8, 4554 DOI: 10.1039/D1QO00705J

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements