Oxidative Formation of Disulfide Bonds by a Chemiluminescent 1,2-Dioxetane under Mild Conditions

Sauer C, Köckenberger J, Heinrich M (2020)

Publication Type: Journal article

Publication year: 2020

Journal

Journal of Organic Chemistry American Chemical Society

Book Volume: 85

Pages Range: 9331-9338

Journal Issue: 14

DOI: 10.1021/acs.joc.0c00569

Abstract

The oxidation of alkyl thiols to disulfides has been achieved under mild conditions using a chemiluminescent 1,2-dioxetane as a stoichiometric oxidant. Besides the mild and biocompatible reaction conditions, this approach offers the possibility to monitor the presence of thiols through oxidation and chemiluminescence of the remaining dioxetane.

Authors with CRIS profile

Caroline Sauer Lehrstuhl für Pharmazeutische Chemie Johannes Köckenberger Lehrstuhl für Pharmazeutische Chemie Markus Heinrich Professur für Pharmazeutische Chemie

How to cite

APA:

Sauer, C., Köckenberger, J., & Heinrich, M. (2020). Oxidative Formation of Disulfide Bonds by a Chemiluminescent 1,2-Dioxetane under Mild Conditions. Journal of Organic Chemistry, 85(14), 9331-9338. https://dx.doi.org/10.1021/acs.joc.0c00569

MLA:

Sauer, Caroline, Johannes Köckenberger, and Markus Heinrich. "Oxidative Formation of Disulfide Bonds by a Chemiluminescent 1,2-Dioxetane under Mild Conditions." Journal of Organic Chemistry 85.14 (2020): 9331-9338.

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