Selective Electrosynthetic Hydrocarboxylation of a,bUnsaturated Olefins with Carbon Dioxide

08 April 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Electrosynthetic hydrocarboxylation of alpha,beta-unsaturated olefins with excellent regioselectivity is reported. No sacrificial electrode is required and is thus amenable to a flow configuration. The products are purified by simple crystallisation. Synthesis of a precursor to ethosuximide, which contains an all-carbon quaternary centre, illustrates the potential of the process. Finally a robustness study has benchmarked the process for future users.

Keywords

Carbon Dioxide
Electrosynthesis
olefin
alkene
unsaturated ester

Supplementary weblinks

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.