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filingDate 1982-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1988-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9214ca94cd2ac8a31a49d061a9205fe7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9867063e7640a05f7ad0e0f0ad30ef7c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bc05f51bcd8f7db27da3d4f4fcb24053
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6214fb34099fd1be9b70979cb5161709
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89be9ad741a0e68443ec64b5917dc6ca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a386fcadd45505a20530c9f8687d2193
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c71edcde42d41c47bde92416ea700f9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_917524cab07b80f730fb9f816c58f359
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publicationDate 1988-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1442067-A3
titleOfInvention Method of producing derivatives of 2-arylpropyl ethers or thio ether
abstract 2-Arylpropyl ether or thioether derivatives represented by the following general formula [I]: <IMAGE> [I] wherein Ar stands for an aryl group, R stands for a methyl or ethyl group, Y stands for an oxygen or sulfur atom, and B stands for a group represented by the following formula [II]: <IMAGE> [II] or the following general formula [III]: <IMAGE> [III] wherein Z stands for an oxygen or sulfur atom or a carbonyl or methylene group, R1 stands for a hydrogen or halogen atom or a lower alkyl group or a lower alkoxy group, and n is an integer of from 1 to 5 with the proviso that when n is 2 or more, the groups R1 may be the same or different, are produced by reacting a compound represented by the following formula (V): <IMAGE> (V) with a compound represented by the following formula (VI): B-CH2-D (VI) wherein Ar, R and B are defined above, A is a halogen atom and D is Y-H in which Y is as defined above, in the presence of a base in dimethylsulfoxide or sulfolane. The compounds thus prepared have excellent insecticidal and acaricidal activities while the toxicity of these compounds are very low.
priorityDate 1980-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 479.