http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H05148221-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-757
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-258
filingDate 1991-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_43441dc1799535047aa77f1c4c9f77dc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0676f7f37c64addc743a734efa0948c
publicationDate 1993-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05148221-A
titleOfInvention Vinyl ether derivative, production method thereof and use thereof
abstract (57) [Summary] (Modified) [Objective] To provide a vinyl ether derivative useful as an intermediate for medicines, agricultural chemicals, fragrances, analytical reagents and the like. [Structure] A method for producing a vinyl ether derivative of the general formula [1], which comprises reacting a vinyl ether derivative of the general formula [1] and an alkenylthioether with a lithiating agent, and further reacting with an α, β-unsaturated ketone; A method for producing this unsaturated ketoaldehyde using a ketoaldehyde and a vinyl ether derivative. [Wherein, R 1 is alkyl, aryl, aralkyl, R 2 Is H, alkyl, aryl, aralkyl or alkylene together with R 1 , R 3 is aryl, R 4 and R 5 are H, Alkyl, R 6 represents alkyl] Specific examples of the compounds of the general formulas [1] and [4] include 3- (1-phenylthio-3-methoxy-2-propenyl) -cyclohexanone and 3- (2-formyl-ethenyl) -cyclohexanone, respectively.
priorityDate 1991-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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