Stereoselective synthesis of amino acid derivatives using carbohydrates as templates

dc.contributor.authorKunz, Horstde
dc.contributor.authorSager, Wilfriedde
dc.contributor.authorPfrengle, Waldemarde
dc.contributor.authorLaschat, Sabinede
dc.contributor.authorSchanzenbach, Dirkde
dc.date.accessioned2010-06-24de
dc.date.accessioned2016-03-31T11:42:38Z
dc.date.available2010-06-24de
dc.date.available2016-03-31T11:42:38Z
dc.date.issued1993de
dc.date.updated2014-10-16de
dc.description.abstractGlycosylamines 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.en
dc.identifier.other325219850de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-54563de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/7304
dc.identifier.urihttp://dx.doi.org/10.18419/opus-7287
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationAminosäuren , Stereoselektive Synthesede
dc.subject.ddc540de
dc.titleStereoselective synthesis of amino acid derivatives using carbohydrates as templatesen
dc.typearticlede
ubs.fakultaetFakultätsübergreifend / Sonstige Einrichtungde
ubs.institutSonstige Einrichtungde
ubs.opusid5456de
ubs.publikation.sourceChemistry of peptides and proteins 12 (1993), no. 5/6, S. 91-98de
ubs.publikation.typZeitschriftenartikelde

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