http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H06279338-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a77d66ff67a9626dd7de5cce2097afcd |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-159 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N63-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-035 |
filingDate | 1993-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd473522c5dfc01afd29e717137f8ebc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_454d00a03ea23159041ad64bb5beeba7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_513fd2638dbcd2d0f067d2878b2c3501 |
publicationDate | 1994-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H06279338-A |
titleOfInvention | Process for producing meso- (3E, 7E) -5,6-bis (hydroxymethyl) -3,7-decadiene |
abstract | (57) [Summary] (Modified) [Purpose] Citrus pests (Hemiptera: Biprorulus) bibaxBreddin) can be synthesized in good yield and high purity as a synthetic intermediate of the attractive pheromone. [Structure] 2 (E) -hexene-1,4-diol A first step of reacting with butyldimethylsilyl chloride / a second step of reacting the formation with 3 (E) -hexenoic acid / a trimethylsilyl etherification of the formation with trimethylsilyl chloride followed by a rearrangement reaction followed by acid Third step of hydrolyzing with / The product is reduced to give meso- (3 E, 7E) -5,6-bis (hydroxymethyl) -3. It consists of a fourth step to form 7-decadiene. |
priorityDate | 1993-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 60.