Your browser doesn't support javascript.
loading
Selective transamidation of 3-oxo-N-acyl homoserine lactones by hydrazine derivatives.
Bertucci, Michael A; Lee, Stephen J; Gagné, Michel R.
Affiliation
  • Bertucci MA; Department of Chemistry, University of North Carolina at Chapel Hill, Campus Box 3290, Caudill and Kenan Laboratories, Chapel Hill, NC 27599-3290, USA. mgagne@unc.edu.
Org Biomol Chem ; 12(37): 7197-200, 2014 Oct 07.
Article de En | MEDLINE | ID: mdl-25139543
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.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: 4-Butyrolactone / Hydrazines Langue: En Journal: Org Biomol Chem Sujet du journal: BIOQUIMICA / QUIMICA Année: 2014 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: 4-Butyrolactone / Hydrazines Langue: En Journal: Org Biomol Chem Sujet du journal: BIOQUIMICA / QUIMICA Année: 2014 Type de document: Article Pays d'affiliation: États-Unis d'Amérique