Kunz, HorstSager, WilfriedPfrengle, WaldemarLaschat, SabineSchanzenbach, Dirk2010-06-242016-03-312010-06-242016-03-311993325219850http://nbn-resolving.de/urn:nbn:de:bsz:93-opus-54563http://elib.uni-stuttgart.de/handle/11682/7304http://dx.doi.org/10.18419/opus-7287Glycosylamines contain the easily cleavable semi-aminal-type N-glycosidic bond. O-Protected glycosylamines, therefore, can advantageously be used as a form of "asymmetric ammonia", for instance, in Strecker syntheses and in Ugi reactions to give amino acid amides as well as in modifications of the Mannich reaction.eninfo:eu-repo/semantics/openAccessAminosäuren , Stereoselektive Synthese540Stereoselective synthesis of amino acid derivatives using carbohydrates as templatesarticle2014-10-16