Stereocontrolled Backbone Connection of Peptides by C C-Double Bonds
S Schumann, K Zeitler, M Jäger, K Polborn, W Steglich
Index: Schumann, Susanne; Zeitler, Kirsten; Jaeger, Martin; Polborn, Kurt; Steglich, Wolfgang Tetrahedron, 2000 , vol. 56, # 25 p. 4187 - 4195
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Citation Number: 17
Abstract
Treatment of peptides containing an α-chloroglycine residue with triethylamine and catalytic amounts of triphenylphosphine constitutes an efficient method for the stereoselective synthesis of amino acid and peptide dimers bridged by a C C-double bond. The dimers can be converted into novel peptide structures by standard methods of peptide synthesis.
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