http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1310127-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_126c4d65cf72bb294bd55272f71c328c |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C47-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B35-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C47-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B35-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A47B65-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-00 |
| filingDate | 1970-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1973-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1310127-A |
| titleOfInvention | Process for oxidising organic compounds |
| abstract | 1310127 Oxidation reactions WASAGCHEMIE AG 20 May 1970 [20 May 1969] 24347/70 Heading C2C Complex lead (IV) acids having ligands which are either all the same or are different and which may be substituted or esterified and/or salts of such acids can be used to oxidize diols, hydroquinone compounds, alcohols, amine and hydrazine compounds and unsaturated compounds in aqueous or alcoholic solution. Examples prepare formaldehyde from 1,2-ethanediol, acetaldehyde from 2,3-butanediol, glyoxylic acid from tartaric acid, p-benzoquinone from p - hydrobenzoquinone and glycol aldehyde from vinyl ethyl ether. Reference is also made to the production of butyraldehyde from octene-4, cyanacetaldehyde from 1,4- dicyano-2-butene and acetone from 2,3-dimethyl-2-butene. |
| priorityDate | 1969-05-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 42.