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A new strategy to produce beta-peptides: use of alicyclic beta-lactams
Ferenc Fülöp1, Enikö Forró, Gábor K Tóth
1Institute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, Eötvös u. 6, Hungary. fulop@pharma.szote.u-szeged.hu
Abstract:
On p-methylbenzhydrylamine (MBHA) resin, by means of t-Boc chemistry, several tetrapeptides (H-Ala-ACXC-Ala-Gly-NH(2)) containing cyclic beta-amino acid units were prepared. These units were introduced into the growing peptide chain by using Boc-protected beta-lactams with KCN as catalyst in DMF. The method was applicable for both racemic and enantiomeric beta-lactams.
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