Synthesis of a Gln-Phe Hydroxy-ethylene Dipeptide Isostere
Organic Letters2004Vol. 6(25), pp. 4783–4786
Citations Over TimeTop 21% of 2004 papers
Abstract
[structure: see text] The protected Gln-Phe hydroxyethylene dipeptide isostere 1 was synthesized as a precursor for preparation of potential inhibitors of Botulinum neurotoxin B metalloprotease. The method allows for the synthesis of additional hydroxyethylene dipeptide isosteres such as 2 with functionalized P1 side chains. The isosteres prepared were coupled with a dipeptide to produce protected pseudotetrapeptide derivatives.
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