http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1855529-B1
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_981a37900e6991fb373304ed2ba5a703 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D493-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-113 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-90 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-30 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-36 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-36 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-10 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-10 |
filingDate | 2006-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2013-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3ac87f4575fb03745bd0e6a34b1f4213 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b6cfdc130fc946046545223fe361ac9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_facee8c9f24bed5f885b782c15c10d6e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b673cf1637a9a8225db08f072ef9e91d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_787835e2c05c5fe0b2e9035c11188e80 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39bc8d7af376f7506004f803400e3ad2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eda03a4f14890a7bbfd0b472ddd2fa83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db2b456c09ff682237fd8b1713cf2607 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a9dfa2b7dd5ac9b4001cc6efc4fd9996 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_974b8433ef3f39171ce9e16249caf9f7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_144c8fcf218368c57ec3f439ec5f5e99 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cd28a360aaf28eb724012ee6792a938c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae62cc9e48bc06b030811445bf88673b http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_28e42e0b74cd638e260dbd298e0f4d6e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_200b37923d04e66cf0fa06e0bf62131a |
publicationDate | 2013-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | EP-1855529-B1 |
titleOfInvention | Spiroketal-substituted cyclic ketoenols |
abstract | Spiroketal-substituted cyclic ketoenol compounds (I) are new. Spiroketal-substituted cyclic ketoenol compounds of formula (I) are new. W1>H, (halo)alkyl, alkenyl, alkynyl, (halo)alkoxy, halo, alkenyloxy or CN; X : halo, (halo)alkyl, alkenyl, alkynyl, (halo)alkoxy, (halo)alkenyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, nitro or CN; Y1>, Z : H, (halo)alkyl, alkenyl, alkynyl, (halo)alkoxy, halo, nitro, CN or optionally substituted (het)aryl (provided that at least one of W1> or Z is H when X and Y1> are CH3); C+A+B1>(halo)alkyl, alkoxy, alkoxyalkyl or optionally substituted phenyl substituted 5-7 membered ketal or (di)thioketal, which is interrupted through a further heteroatom; D : NH or O; Q1>, Q2>H, haloalkyl or alkoxy; G : H, -C(=O)-R1>, -C(=L)-M-R2>, -SO2-R3>, -P(=L)(R4>)(R5>), E or -C(=L)-N(R6>)(R7>); E : metal ion or ammonium ion; L, M : O or S; R1>alkyl, alkenyl, (poly)alkoxyalkyl, alkylthioalkyl (all optionally substituted with halo or CN), cycloalkyl or heterocyclyl (both optionally substituted with halo, alkyl or alkoxy) or optionally substituted (phenyl)alkyl, hetaryl, phenoxyalkyl or hetaryloxyalkyl; R2>alkyl, alkenyl or (poly)alkoxyalkyl (all optionally substituted with halo or CN) or optionally substituted cycloalkyl, phenyl or benzyl; R3>-R5>alkyl(thio), alkoxy, (di)alkylamino, alkenylthio or cycloalkylthio (all optionally substituted with halo) or optionally substituted phenyl, benzyl, phenoxy or phenylthio; and either R6>, R7>(cyclo)alkyl, alkenyl, alkoxy, alkoxyalkyl (all optionally substituted with halo or CN), phenyl, benzyl (both optionally substituted) or H; or NR6>R7>optionally substituted ring optionally containing O or S. Independent claims are included for: (1) N-cyclohexyl-2-phenyl-acetamide compounds of formula (II); (2) phenyl-acetic acid cyclohexyl ester compounds of formula (III); (3) 1-phenylacetylamino-cyclohexanecarboxylic acid compounds of formula (XVIII); (4) N-(1-cyano-cyclohexyl)-2-phenyl-acetamide compounds of formula (XXI); (5) 1-amino-cyclohexanecarbonitrile compounds of formula (XX); (6) substituted cyclohexanol compounds of formula (XXII); (7) 1,4-dioxa-spiro[4.5]dec-8-ylamine compounds of formula (XVI') or (XVI''); (8) 8-amino-1,4-dioxa-spiro[4.5]decane-8-carbaldehyde compounds of formula (XIX'); (9) 9-amino-1,5-dioxa-spiro[5.5]undecane-9-carboxylic acid compounds of formula (XIX''); (10) 9,12-dioxa-1,3-diaza-dispiro[4.2.4.2]tetradecane-2,4-dione compounds of formula (XXIII'); (11) 9,13-dioxa-1,3-diaza-dispiro[4.2.5.2]pentadecane-2,4-dione compounds of formula (XXIII''); (12) the preparation of (I); (13) an agent, for combating animal parasites, undesired plant growth and/or undesired microorganisms, comprising (I); (14) a method for combating animal parasites, undesired plant growth and/or undesired microorganisms comprising applying (I) on the parasites, undesired plant and undesired microorganisms and/or their habitats; (15) a method for preparing the agent comprising mixing (I) with diluting agents and/or surface active substances; (16) an agent comprising an active combination comprising (I) and at least one culture plant compatibility improving 59 compounds e.g. 4-dichloracetyl-1-oxa-4-aza-spiro[4.5]-decane, 1-(1-methyl-1-phenyl-ethyl)-3-(4-methyl-phenyl)-urea, piperidin-1-thiocarboxylic acid-S-1-methyl-1-phenyl-ethylester, 2,2-dichloro-N,N-di-2-propenyl-acetamide and 1-(ethoxycarbonyl)-ethyl-3,6-di-chloro-2-methoxybenzoate; (17) a method for combating undesirable plant growth comprising applying the agent on the plant or its surrounding; and (18) a method for combating undesirable plant growth comprising applying (I) and the culture plant compatibility increasing compounds in a temporary nearer sequence on the plants or their surroundings. In formula (XVI'): Q3>1-4C alkyl, 1-3C haloalkyl, 1-4C alkoxy or 1-4C alkoxy-1-4C alkyl; and q : 1-3. In formulae (XVI''), (XIX''), (XXIII''):q = 0-3. In formulae (XIX'), (XXIII'): q : 1-3. [Image] [Image] [Image] [Image] [Image] [Image] - ACTIVITY : Antiparasitic; Herbicide; Antibacterial; Antimicrobial. The |
priorityDate | 2005-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
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