http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-WO2013125688-A1
Outgoing Links
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|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2231-70 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2527-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2603-52 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D451-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0234 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2278 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-313 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2273 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-0271 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B63-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D221-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C45-29 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-006 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D221-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-27 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C47-263 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-29 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J37-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02 |
| filingDate | 2013-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2015-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-WO2013125688-A1 |
| titleOfInvention | 9-azanoradamantane N-oxyl compound and method for producing the same, organic molecular oxidation catalyst using 9-azanoradamantane N-oxyl compound, and method for oxidizing alcohols |
| abstract | In relation to an organic molecular catalyst that oxidizes alcohols, a primary alcohol is selectively oxidized in a polyol substrate having a plurality of alcohols under conditions excellent in environmental harmony. An organic oxidation catalyst for oxidizing alcohols, wherein an oxygen atom is bonded to a nitrogen atom of an azanoradamantane skeleton and has at least one alkyl group at the 1-position and 5-position. INDUSTRIAL APPLICABILITY According to the present invention, there is provided an oxidation catalyst having higher activity than TEMPO, which is an existing oxidation catalyst in a primary alcohol selective oxidation reaction, and being more selective than AZADO and 1-Me-AZADO. In addition, DMN-AZADO according to the present invention can be applied to a primary alcohol selective oxidation reaction that contributes to the shortening of the synthesis of high-value-added organic compounds such as pharmaceuticals, pharmaceutical raw materials, agricultural chemicals, cosmetics, and organic materials. it can. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11573488-B2 |
| priorityDate | 2012-02-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 255.