CrCl 2 mediated allylation of N-protected α-amino aldehydes. A versatile synthesis of polypeptides containing an hydroxyethylene isostere
P Ciapetti, M Taddei, P Ulivi
Index: Ciapetti, Paola; Taddei, Maurizio; Ulivi, Paola Tetrahedron Letters, 1994 , vol. 35, # 19 p. 3183 - 3186
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Citation Number: 38
Abstract
Abstract Differently substituted allylic bromides react with N-protected amino aldehydes to give intermediate products for the synthesis of hydroxyethylene dipeptide isosteres. The low stereoselectivity of this reaction can be improved using aldehydes protected with hindered groups. This reaction can be efficiently applied to oligopetide aldehydes. We describe a protocol, for the preparation of peptides containing an hydroxyethylene isostere, which ...
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