| Literature DB >> 20014826 |
Brigitte Guérin1, Samia Ait-Mohand, Marie-Claude Tremblay, Véronique Dumulon-Perreault, Patrick Fournier, François Bénard.
Abstract
A convenient approach to functionalize peptides either at the N-terminal or on a lysine side chain with 1,4,7-triazacyclononane-N,N',N''-triacetic acid (NOTA) chelating unit has been developed on solid support. The chelate was assembled in a two-step process starting with bromo-acetylated peptides. Deprotection and cleavage of the resin-bound NOTA peptides were performed with use of trifluoroacetic acid (TFA) in the presence of thioanisole and water to give free NOTA peptides.Entities:
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Year: 2010 PMID: 20014826 DOI: 10.1021/ol902601x
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005