Current electrochemical approaches to selective deuteration

Philip L. Norcott*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    45 Citations (Scopus)

    Abstract

    The selective deuteration of organic molecules through electrochemistry is proving to be an effective alternative to conventional 2H labelling strategies, which traditionally require high temperatures, high pressures of deuterium gas in hydrothermal autoclave reactors, or require reagents capable of generating highly reactive species which are then quenched by a deuterium source. Such harsh conditions or reagents can consequently lower chemo- or regioselectivity in many deuteration processes. Transition metal catalysis and more recently photocatalysis have emerged as methods to access selectively deuterated compounds under significantly more mild conditions. Now, electrochemistry, which is increasingly becoming a mainstream synthetic tool, is primed to enter this space. Accordingly, this highlight will feature a selection of electrochemical deuteration methods developed in recent years, and propose where the use of electrosynthesis could access novel reactivity in the context of deuteration.

    Original languageEnglish
    Pages (from-to)2944-2953
    Number of pages10
    JournalChemical Communications
    Volume58
    Issue number18
    DOIs
    Publication statusPublished - 4 Mar 2022

    Fingerprint

    Dive into the research topics of 'Current electrochemical approaches to selective deuteration'. Together they form a unique fingerprint.

    Cite this