Issue 85, 2024

New electrophiles targeting thiols in a reversible covalent manner

Abstract

Reversible covalent electrophiles with the advantages of both reversible and covalent interactions receive much attention in the fields of chemical biology and medicinal chemistry. Here, we report two electron-deficient olefins activated by amide and ester, amide-substituted acrylamide and methyl ester-substituted acrylamide, targeting thiols in a reversible covalent manner.

Graphical abstract: New electrophiles targeting thiols in a reversible covalent manner

Supplementary files

Article information

Article type
Communication
Submitted
07 Sep 2024
Accepted
30 Sep 2024
First published
09 Oct 2024

Chem. Commun., 2024,60, 12437-12440

New electrophiles targeting thiols in a reversible covalent manner

X. Ma, M. Xu, F. Wang, T. Hu, X. Chen and C. Zhang, Chem. Commun., 2024, 60, 12437 DOI: 10.1039/D4CC04612A

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