http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9311255-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1bfbfb78646e8428e5f0cbb5e833b156 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P41-006 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12P7-24 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P7-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12P41-00 |
| filingDate | 1992-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4208b48a5f0a5e148df99d890c71575a |
| publicationDate | 1993-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | WO-9311255-A1 |
| titleOfInvention | Process for preparing optically active cyanohydrines by racemate separation in the presence of oxynitrilases |
| abstract | A process is disclosed for preparing optically active cyanohydrines by splitting an enantiomer cyanohydrine mixture. Only one enantiomer of the mixture is split in the presence of oxynitrilases into the corresponding carbonyle compound and hydrocyanic acid. The hydrocyanic acid thus obtained is transferred to another carbonyl compound having a stronger affinity for hydrocyanic acid than the carbonyl compound obtained through splitting. It thus becomes possible to carry out racemate splitting up to semi-conversion even at higher concentration, although the chemical balance lies in general largely on the side of the cyanohydrine. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9963104-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0561535-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0561535-A3 |
| priorityDate | 1991-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 23.