Diastereoselective Alkylation of Schiff Bases for the Synthesis of Lipidic Unnatural Fmoc??Protected α??Amino Acids

…, F Nuti, J Uziel, M Ginanneschi, M Chelli…

Index: Papini, Anna Maria; Nardi, Elena; Nuti, Francesca; Uziel, Jacques; Ginanneschi, Mauro; Chelli, Mario; Brandi, Alberto European Journal of Organic Chemistry, 2002 , # 16 p. 2736 - 2741

Full Text: HTML

Citation Number: 9

Abstract

Abstract Peptides with increased lipophilicity can cross cell membranes more easily and have longer half-life times. For these reasons, the synthesis of enantiomerically pure Fmoc- protected lipidic α-amino acids is a relevant goal. Schiff bases originating from the reaction between the two enantiomers of 2-hydroxypinan-3-one with Gly-OtBu were alkylated with a series of long alkyl halides. Diastereomeric excesses were determined by reversed-phase ...

Related Articles:

Synthesis of Unnatural Lipohilic N??(9H??Fluoren??9??ylmethoxy) carbonyl??Substituted α??Amino Acids and Their Incorporation into Cyclic RGD??Peptides: A structure?? …

[Koppitz, Marcus; Huenges, Martin; Gratias, Rainer; Kessler, Horst; Goodman, Simon L.; Jonczyk, Alfred Helvetica Chimica Acta, 1997 , vol. 80, # 4 p. 1280 - 1300]

More Articles...