http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-413942-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9af6f947243f3e10fbd19fc7221bfc4f |
classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-685 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P17-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-32 |
filingDate | 2015-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11927618512855d17729d20913398043 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0a4d9a17e20082732341f1bdf78cbed2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9ddb3b9210af807cc0ac80b3cf994f85 |
publicationDate | 2017-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | PL-413942-A1 |
titleOfInvention | A method for producing optically pure (+) - (R) -7-hydroxyflavanone |
abstract | It was revealed that as a result of the enzymatic system contained in the cells of the Aspergillus niger IBR strain, de-esterification occurs at C-7. The product thus obtained is separated from the aqueous culture of the microorganism in a known manner by extraction with a water-immiscible organic solvent (ethyl acetate). The result is (+) - (R) -7-hydroxyflavanone with an enantiomeric excess of 100% ee, at room temperature and at the natural pH for the strain. |
priorityDate | 2015-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 20.