http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0184173-A2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3e9445e5e3626f36e932c6451a928250 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-01 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P33-10 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-01 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P33-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-365 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-35 |
| filingDate | 1985-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2f68597e8141bd544a3ee6cb0b6410f8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca29c495554e4cb6d94be3ee26817350 |
| publicationDate | 1986-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | EP-0184173-A2 |
| titleOfInvention | 13beta-milbemycine derivatives for the control of ectoparasites and endoparasites in plants and animals |
| abstract | R, Wasserstoff oder eine Schutzgruppe bedeutet; R 2 für Methyl, Ethyl, Isopropyl oder sek.Butyl steht; und R für einen über Sauerstoff oder Schwefel gebundenen Rest R 3 , ausgewählt aus der Reihe C 1 -C 10 -Alkyl, C 1 -C 10 -Haloalkyl, C 1 -C 10 -Hydroxyalkyl, C 1 -C 10 -Mercaptoalkyl, C 2 -C 10 -Alkoxyalkyl, C 3 -C, o -Alkoxyalkoxyalkyl, durch Hydroxy oder Mercapto substituiertes C 3 -C 10 -Alkoxyalkoxyalkyl, C 4 -C 15 -Alkoxyalkoxyalkoxyalkyl, durch Hydroxy oder Mercapto substituiertes C4-C,s-Alkoxyalkoxyalkyl, C 2 -C lo -Alkenyl, C 2 -C, o -Haloalkenyl, C 2 -C 10 -Alkinyl, C 2 -C 10 -Haloalkinyl, unsubstituiertes oder durch Halogen, C 1 -C 3 -Alkyl, C 1 -C 3 -Haloalkyl, C,-C 3 -Alkoxy, C,-C 3 -Haloalkoxy, Cyano und/oder Nitro substituiertes Phenyl und unsubstituiertes oder durch Halogen, C 1 -C 3 -Alkyl, C,-C 3 -Haloalkyl, C,-C 3 -Alkoxy, C l -C 3 -Haloalkoxy, Cyano und/oder Nitro substituiertes Benzyl steht, oder R eine der Gruppen -SH oder -S-C(0)OR 4 repräsentiert, wobei R 4 für C 1 -C 10 -Alkyl, C 1 -C 10 -Haloalkyl oder eine unsubstituierte oder durch Halogen, C,-C 3 -Alkyl, C 1 -C 3 -Haloalkyl, C 1 -C 3 -Alkoxy, C l -C 3 -Haloalkoxy, Cyano und/oder Nitro substituierte Gruppe aus der Reihe Phenyl und Benzyl steht, beschrieben, sowie ihre Herstellung ausgehend von den entsprechend substituierten 15-Hydroxi- bzw. 13ß-Hydroxi-Milbemycinen der Formel II. There are parasiticidal and insecticidal highly active ingredients of formula I. wherein R represents hydrogen or a protecting group; R 2 represents methyl, ethyl, isopropyl or sec-butyl; and R for a radical R 3 bonded via oxygen or sulfur, selected from the series C 1 -C 10 alkyl, C 1 -C 10 haloalkyl, C 1 -C 10 hydroxyalkyl, C 1 -C 10 mercaptoalkyl, C 2 -C 10 alkoxyalkyl, C 3 -C, o -Alkoxyalkoxyalkyl, by hydroxy or mercapto-substituted C 3 -C 10 -Alkoxyalkoxyalkyl, C 4 -C 15 -Alkoxyalkoxyalkoxyalkyl, by hydroxy or mercapto-substituted C4-C, s-alkoxyalkoxyalkyl, C 2 -C lo alkenyl, C 2 -C, o haloalkenyl, C 2 -C 10 alkynyl, C 2 -C 10 haloalkynyl, unsubstituted or substituted by halogen, C 1 -C 3 alkyl, C 1 -C 3 -Haloalkyl, C, -C 3 -alkoxy, C, -C 3 -haloalkoxy, cyano and / or nitro substituted phenyl and unsubstituted or halogen, C 1 -C 3 -alkyl, C, -C 3 -haloalkyl, C, -C 3 alkoxy, C l -C 3 haloalkoxy, cyano and / or nitro substituted benzyl, or R represents one of the groups -SH or -SC (0) OR 4 , where R 4 is C 1 -C 10 - Alkyl, C 1 -C 10 haloalkyl or an unsubstituted or by halogen, C, -C 3 alkyl, C 1 -C 3 -Haloalkyl, C 1 -C 3 -alkoxy, C 1 -C 3 -haloalkoxy, cyano and / or nitro substituted group from the series phenyl and benzyl is described, and their preparation based on the correspondingly substituted 15-hydroxyl or 13β-Hydroxy-milbemycins of the formula II. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0444964-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0448243-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4859657-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008136791-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0214731-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7919522-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5604182-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0341972-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0341972-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0357460-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4897416-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0594291-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5346918-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0430884-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101679451-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0235085-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0252879-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0552817-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0552818-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0279783-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0214731-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0552817-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0552818-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0284563-A3 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0530901-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0506331-A1 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0284563-A2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0357460-A2 |
| priorityDate | 1984-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 253.