http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2017081933-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_046e16bd6918ef3cd62184605b15a413 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-21 |
| filingDate | 2016-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5de6f18fac57d471a6188f8c24a07d1 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3509ddb4e4ef43baadb232ab13a957ca |
| publicationDate | 2017-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2017081933-A |
| titleOfInvention | Process for producing optically active 2,3-dihydrofarnesal |
| abstract | Provided are a synthetic intermediate useful for obtaining optically active 2,3-dihydrofarnesal having high chemical purity and optical purity, and an efficient method for producing the intermediate. An optically active fernesyl enamine represented by the formula (4). (* Is an asymmetric carbon atom; R1 and R2 are each independently H, substituted / unsubstituted C1-20 alkyl group, substituted / unsubstituted 3- to 8-membered alicyclic group, substituted / unsubstituted. C6-15 aryl group, substituted / unsubstituted C2-15 heterocyclic group or substituted / unsubstituted C7-12 aralkyl group; R1 and R2 are not H at the same time or R1 and R2 are bonded A ring may be formed) [Selection figure] None |
| priorityDate | 2016-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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