Sauer C, Köckenberger J, Heinrich M (2020)
Publication Type: Journal article
Publication year: 2020
Book Volume: 85
Pages Range: 9331-9338
Journal Issue: 14
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.
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://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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