http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2760841-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_99505f5f312672820e9f78c254c00a4d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01R33-465
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01R33-465
filingDate 1997-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_218143f900aa2db2ac32cda4e6840fa7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22a30ddc736d0f8b198760a5a2200387
publicationDate 1998-09-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2760841-A1
titleOfInvention DETERMINATION BY NUCLEAR MAGNETIC RESONANCE OF THE ABSOLUTE CONFIGURATION OF AMINO ACIDS OR THEIR DERIVATIVES AND METAL COMPLEXES OF CHIRAL PORPHYRINS USABLE FOR THIS DETERMINATION
abstract The invention relates to novel metal complexes of chiral porphyrins of formula (I) capable of binding to an axial coordination site an alpha-amino acid or a derivative thereof carrying an asymmetric carbon, and of acting thus the role of chiral chemical shifting agent. Complexation in the vicinity of porphyrin causes high-field displacement of alpha-amino acid proton NMR signals, as well as changes in some porphyrin proton NMR signals. These shifts are characteristic of the R or S configuration of asymmetric carbon. Examination of the 1 H NMR spectrum thus constitutes an easy means for determining the absolute configuration of the alpha-amino acid or derivative, as well as for detecting the racemization of these compounds.
priorityDate 1997-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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