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filingDate 1989-01-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6e2606cce87c940d990d2304dd0f5231
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_467815e153b181b7ac1d86915be0810a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9bc98945146f7e864b39dd2fd04a5200
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3de105869bf13d625961409c489f29e2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_832b20eede0855d2f60e61f1cdbf86b5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47cb624f198fff02d88a4978c128dbdf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94b5bda185001f3fa056291adb8e4557
publicationDate 1990-01-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H021422-A
titleOfInvention Improvement in organic compound
abstract NEW MATERIAL: Dione compounds of formula I [R 1 -R 4 are unsaturated aliphatic hydrocarbon residue, cycloalkyl, Ar, (A 1 )nX (Ar is 5-6 membered heteroaryl; n is 0 or 1; X is H, NO 2 , halogen, CN, benzyl, etc.; A 1 is methylene or ethylene); A 2 is bond, O, S, CO, etc.; A 3 -A 4 are each C=C(OR a ) or C(X 1 )-C(O) (R a is H or salt forming part, OR a is ester part, etc.; X 1 is F or Cl); Y is pghenyl, heteroaromatic group]. n EXAMPLE: 2-(1-Methyl-4-nitro-5-pyrazolylcarbonyl)-1,3-cyclohexanedione. n USE: Herbicide. n PROCESS: A compound of formula II is reacted with a compound of a formula Y-CO-Hal (Hal is halogen), and a compound of formula IV is obtained by the rearrangement of a resultant compound of formula III. n COPYRIGHT: (C)1990,JPO
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priorityDate 1988-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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