Issue 37, 2014

Selective transamidation of 3-oxo-N-acyl homoserine lactones by hydrazine derivatives

Abstract

A method for the selective transamidation of the 3-oxo sub-family of N-acyl homoserine lactones (3-oxo-AHLs) under physiologically relevant conditions has been developed. The reaction has the potential to serve as a strategy for selective knockdown of key autoinducers in a multicellular environment.

Graphical abstract: Selective transamidation of 3-oxo-N-acyl homoserine lactones by hydrazine derivatives

Supplementary files

Article information

Article type
Communication
Submitted
04 Jun 2014
Accepted
12 Aug 2014
First published
12 Aug 2014

Org. Biomol. Chem., 2014,12, 7197-7200

Author version available

Selective transamidation of 3-oxo-N-acyl homoserine lactones by hydrazine derivatives

M. A. Bertucci, S. J. Lee and M. R. Gagné, Org. Biomol. Chem., 2014, 12, 7197 DOI: 10.1039/C4OB01156B

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