Tetrahydroxydiboron-Mediated Palladium-Catalyzed Deoxygenative Transfer Hydrogenation of Aryl Ketones

21 April 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

We describe a palladium-catalyzed deoxygenative transfer hydrogenation of ketones using B2(OH)4 as the sole additive. Deuterium labeling experiments using B2(OD)4 show that the incorporated protons originate exclusively from the diboron reagent. Spectroscopic evidence implicates the intermediacy of a borate ester. A wide array of aromatic ketones can be deoxygenated using this approach.

Keywords

catalytic transfer hydrogenation
palladium catalysis
deuterium labeling
tetrahydroxydiboron
ketone deoxygenation

Supplementary materials

Title
Description
Actions
Title
Supporting Information
Description
Supporting information for Tetrahydroxydiboron-Mediated Palladium-Catalyzed Deoxygenative Transfer Hydrogenation of Aryl Ketones
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.