http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001220392-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1010e3862914acdd087e73d76911ec6d |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N21-19 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F3-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-35 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-22 |
filingDate | 2000-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_608a37c25cd4e07a5c8964c73af76321 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5a3a879a2d9bdf48a4231ec268eca63e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_924f067581a9c2bed420da8ae681b3a1 |
publicationDate | 2001-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-2001220392-A |
titleOfInvention | How to determine the absolute configuration of a chiral compound |
abstract | (57) [Summary] [Problem] To provide a general-purpose, absolute configuration of a new chiral compound in which the kinds of basic groups to be bound can accurately and easily determine the absolute configuration of a chiral compound. Provide a decision method. The present invention has a structure of a porphyrin dimer cross-linked by a carbon chain, and extends from the carbon at a cross-linking position of one porphyrin ring of the dimer structure along the outer periphery of the porphyrin ring. Metal porphyrins with a bulky substituent on at least one of the second carbons more than an ethyl group, A chiral compound having an asymmetric carbon to which a basic group capable of coordinating to a metal of the other porphyrin ring in the dimer structure of the metal porphyrin or an asymmetric carbon at a position adjacent to the carbon atom to which the basic group is bonded And determining the absolute configuration of the chiral compound from the sign of the Cotton effect by circular dichroism spectrophotometric analysis. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-4637782-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7736902-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007271592-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7648841-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10309035-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7125725-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2004070364-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-03073076-A1 |
priorityDate | 1999-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 84.