http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2760841-A1
Outgoing Links
Predicate | Object |
---|---|
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 |
Incoming Links
Total number of triples: 73.