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Doan N.-D.,De Partement Of Chimie University Of Montre Al Cp 6128 | Zhang J.,De Partement Of Chimie University Of Montre Al Cp 6128 | Traore M.,De Partement Of Chimie University Of Montre Al Cp 6128 | Kamdem W.,De Partement Of Chimie University Of Montre Al Cp 6128 | Lubell W.D.,De Partement Of Chimie University Of Montre Al Cp 6128
Journal of Peptide Science | Year: 2014

The solid-phase synthesis of azapeptides possessing a C-terminal aza-residue has been accomplished by a protocol featuring regioselective alkylation of benzhydrylidene-aza-glycinamide and illustrated by the syntheses of [aza-Lys6] growth-hormone-releasing peptide-6 analogs. © 2014 European Peptide Society and John Wiley & Sons, Ltd. Source

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