New pyrrole-based amino acids for the synthesis of peptidomimetic constrained scaffolds
M Alongi, G Minetto, M Taddei
Index: Alongi, Maddalena; Minetto, Giacomo; Taddei, Maurizio Tetrahedron Letters, 2005 , vol. 46, # 41 p. 7069 - 7072
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Citation Number: 19
Abstract
A new family of pyrrole-based amino acids have been prepared through the microwave assisted Paal–Knorr reaction of 1–4 ketoesters derived from the corresponding β-ketoester with a functional homologation. The carboxylic group is located in position 3 of the pyrrole, whereas the amino group, protected with the Cbz moiety, is present on the side chain in positions 1 or 2. These compounds were used to prepare constrained oligopeptides.
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