Article
Synthesis of N-Succinyl-L,L-Diaminopimelic Acid Mimetics Via Selective Protection
Protein & Peptide Letters
Document Type
Article
Publication Date
1-1-2010
Disciplines
Abstract
The search for potential inhibitors that target so far unexplored bacterial enzyme mono-N-succinyl-L,Ldiaminopimelic acid desuccinylase (DapE) has stimulated a development of methodology for quick and efficient preparation of mono-N-acylated 2,6-diaminopimelic acid (DAP) derivatives bearing the different carboxyl groups or lipophilic moieties on their amino group.
Citation Information
V. Vanek, J. Picha, M. Budesinsky, M. Sanda, et al.. "Synthesis of N-Succinyl-L,L-Diaminopimelic Acid Mimetics Via Selective Protection" Protein & Peptide Letters (2010) ISSN: 0929-8665 Available at: http://works.bepress.com/richard_holz/1/
Protein & Peptide Letters. Vol. 17, No. 3 (2010): 405-409. DOI.
Richard C. Holz was affiliated with Loyola University-Chicago at the time of publication.