http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0088259-A2

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filingDate 1983-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_73c3e3164dcf32865ef993cb13911efa
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56d655db1d24d14c5bf15d25e92aa7c8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4db11bf4ba11e9eb4c63fb84ed60f132
publicationDate 1983-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0088259-A2
titleOfInvention Azolyl-pyrrolidinones, process for their preparation and their use as fungicides
abstract The invention relates to azolyl-pyrrolidinones of the formula <IMAGE> and their acid addition salts and metal salt complexes, where R1 and R2 are identical or different alkyl radicals having 1 to 3 carbon atoms, R3 and R4 are identical or different substituents with the meaning hydrogen, alkyl with 1 up to 4 carbon atoms and halogen, A represents a keto group, represents a functional derivative of a keto group and represents an alcoholic group of the formula = CH-OH, E represents a nitrogen atom or the> = CH group means X represents substituents selected from the group of the halogens, the cyano and the nitro groups, the alkyl groups with 1 to 3 carbon atoms, the substituted alkyl groups with 1 to 3 carbon atoms, the cycloalkyl groups with 3 to 6 carbon atoms, the alkoxy group with 1 to 3 carbon atoms, the alkylthio groups with 1 to 3 carbon atoms, the alkylsulfonyl groups with 1 to 3 carbon atoms, the acyloxy groups with 1 to 3 carbon atoms toms and the optionally substituted phenyl and pheoxy groups and n is 0 or an integer from 1 to 5. The compounds according to the invention have fungicidal properties.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-8803132-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4902715-A
priorityDate 1982-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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