sodium-cyanoborohydride has been researched along with titanium-tetrachloride* in 1 studies
1 other study(ies) available for sodium-cyanoborohydride and titanium-tetrachloride
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A convenient method for the stereoselective conversion of aryl peptidyl ketones into the corresponding aryl aminomethin derivatives, a novel class of modified peptides.
In this paper we describe a reductive amination procedure that can be employed in the preparation of a novel class of pseudopeptides in which a specific amide bond is replaced by a CH(Ar)NH group. The developed methodology, performed using NaBH(3)CN and TiCl(4), is characterized by the formation of diastereomeric intermediates in a relative 1:1 ratio. It provides aryl aminomethin pseudopeptides in moderate but satisfactory yields and with definite stereochemistry on the asymmetric centres next to the modified peptide bond. Topics: Amination; Benzylamines; Borohydrides; Dipeptides; Indicators and Reagents; Ketones; Molecular Conformation; Peptides; Titanium | 2005 |