Carbohydrates as chiral templates : stereoselective synthesis of (R)- and (S)-α-aminophosphonic acid derivatives

dc.contributor.authorLaschat, Sabinede
dc.contributor.authorKunz, Horstde
dc.date.accessioned2009-07-21de
dc.date.accessioned2016-03-31T11:41:37Z
dc.date.available2009-07-21de
dc.date.available2016-03-31T11:41:37Z
dc.date.issued1992de
dc.date.updated2013-06-12de
dc.description.abstractThe stereoselective synthesis of diethyl (S)- or (R)-α-[(O-pivaloyl-hexapyranosyl) amino]benzylphosphonates is achieved via Lewis acid catalyzed addition of diethyl phosphite to O-pivaloylated N-benzylidene -β-D-galactosylamine or N-benzylidene-α-D-arabinopyranosylamine. The process can also be performed by a one-pot procedure selectively giving (S)-aminophosphonic acid derivatives from galactosylamine and (R)-aminophosphonic acid derivatives from β-L-fucosylamine as the chiral auxiliaries.en
dc.identifier.other314608877de
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-41688de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/7003
dc.identifier.urihttp://dx.doi.org/10.18419/opus-6986
dc.language.isoende
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.subject.classificationKohlenhydrate , Stereoselektive Synthese , Aminophosphonsäurederivatede
dc.subject.ddc540de
dc.titleCarbohydrates as chiral templates : stereoselective synthesis of (R)- and (S)-α-aminophosphonic acid derivativesen
dc.typearticlede
ubs.fakultaetFakultätsübergreifend / Sonstige Einrichtungde
ubs.institutSonstige Einrichtungde
ubs.opusid4168de
ubs.publikation.sourceSynthesis (1992), S. 90-95. URL http://dx.doi.org./10.1055/s-1992-34155de
ubs.publikation.typZeitschriftenartikelde

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
las4.pdf
Size:
458.66 KB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1021 B
Format:
Plain Text
Description: