http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H11509218-A
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D285-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C251-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C255-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C311-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-34 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C251-60 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C253-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C331-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C311-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N37-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-824 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-82 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-734 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C255-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D309-12 |
| filingDate | 1996-07-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1999-08-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H11509218-A |
| titleOfInvention | Oxime ether and acrylic acid derivatives and their use as fungicides |
| abstract | (57) [Summary] Disclosed are ether derivatives having the general formula (I), some processes for their preparation and their use as fungicides, intermediate products and some processes for their preparation. In the formula (I), Ar represents optionally substituted arylene or heteroarylene; E represents ＝ CH— or nitrogen; G is a single bond, oxygen, sulfur or optionally halogen, hydroxy, alkyl, halogenoalkyl or cycloalkyl optionally substituted alkanediyl, alkenediyl, alkynediyl or the following groups -Q-CQ -, - CQ- Q -, - CH 2 -Q -, - Q-CH 2 -, CQ-Q-CH 2 -, - CH 2 -Q- CQ-, Q-CQ-CH 2 -, - Q-CQ-Q-CH 2 -, - n = n -, - S (O) n -, - CH 2 -S (O) n- , -CQ-, -S (O) n -CH 2- , -C (R 3 ) = N-O-, -C (R 3 ) = N-O-CH 2- , -N (R 4) -, - CQ -N (R 4) -, - N (R 4) -CQ -, - Q-CQ-N (R 4) -, - N = (R 3) -Q-CH 2 -, - CH 2 -O-N = C (R 3) -, - C (CH 3) -O-N = C (R 3) -, - N (R 4) -CQ-Q -, - CQ- N (R 4) -CQ-Q -, - N (R 4) -CQ-Q-CH 2 -, - Q-C (R 3) = N-O-CH 2 -, - N (R 4) -C (R 3) = N-O-CH 2 -, - O-CH 2 -C (R 3) = N-O-CH 2 -, - N = N-C ( R 3) = N-OCH 2 -, - C (= N-O-R 5) -C (R 3) = N-OCH 2 -, - C (= N-O-R 5) -C ( R 3) -O-N = CH -, - C (= N-O-R 5) -C (R 3) -O-N = C (CH 3) -, - T-Ar 1 - or -T- Ar 1 -Q- 1 one to represent the; R 1 represents alkoxy, alkylamino or dialkylamino: R 2 is cyano, thiocyanato, Arukiruka Boniru, alkoxycarbonyl, represents aminocarbonyl, amino thiocarbonyl, alkyl aminocarbonyl or dialkylaminocarbonyl; and Z represents alkyl which may be optionally substituted respectively, alkenyl, alkynyl, cycloalkyl, aryl or heterocycle. |
| priorityDate | 1995-07-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 675.