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Bibliografische Daten

Dokument EP000000081893A2 (Seiten: 65)

Bibliografische Daten Dokument EP000000081893A2 (Seiten: 65)
INID Kriterium Feld Inhalt
54 Titel TI [DE] Oxabicycloalkanherbizide.
[EN] Oxabicycloalkane herbicides.
[FR] Herbicides oxabicycloalquiniques.
71/73 Anmelder/Inhaber PA SHELL INT RESEARCH, NL
72 Erfinder IN KOLLMEYER WILLY DIETRICH ; PAYNE GEORGE BERNSON ; POWELL JAMES EDWARD ; ROMAN STEVEN ALAN ; SOLOWAY SAMUEL BARNEY
22/96 Anmeldedatum AD 15.12.1982
21 Anmeldenummer AN 82201609
Anmeldeland AC EP
Veröffentlichungsdatum PUB 22.06.1983
33
31
32
Priorität PRC
PRN
PRD
US
33109481
16.12.1981
33
31
32
PRC
PRN
PRD
US
41657282
13.09.1982
51 IPC-Hauptklasse ICM C07D 493/08
51 IPC-Nebenklasse ICS A01N 43/90
A01N 57/16
A01N 57/24
C07D 493/18
C07F 9/09
C07F 9/38
IPC-Zusatzklasse ICA
IPC-Indexklasse ICI (C07D 493/08, C07D 307:00)
(C07D 493/08, C07D 311:00)
(C07D 493/08, C07D 311:00, C07D 307:00)
(C07D 493/18, C07D 307:00, C07D 303:00)
Gemeinsame Patentklassifikation CPC A01N 43/90
C07C 2601/08
C07C 2601/16
C07C 2602/20
C07C 29/00
C07C 29/106
C07C 29/36
C07C 29/40
C07C 33/12
C07C 33/14
C07C 35/08
C07C 35/38
C07C 43/1781
C07C 45/513
C07D 493/08
MCD-Hauptklasse MCM
MCD-Nebenklasse MCS A01N 43/90 (2006.01)
A01N 57/16 (2006.01)
A01N 57/24 (2006.01)
C07C 29/00 (2006.01)
C07C 29/10 (2006.01)
C07C 29/36 (2006.01)
C07C 29/40 (2006.01)
C07C 33/12 (2006.01)
C07C 33/14 (2006.01)
C07C 35/08 (2006.01)
C07C 35/38 (2006.01)
C07C 43/178 (2006.01)
C07C 45/51 (2006.01)
C07D 493/08 (2006.01)
C07D 493/18 (2006.01)
C07F 9/38 (2006.01)
MCD-Zusatzklasse MCA
57 Zusammenfassung AB [EN] Herbicidal compounds of the general formula <CHEM> wherein X is (-CR4R4-)m in which m is 0 or 1; Y is (-CR5R6-)n in which n is 0, 1 or 2; Z is (-CR7R7-)p in which p is 1,2 or 3; the sum of m + n + p is an integer of from 2 to 5; R1 is a hydrogen atom or a C1-6 alkyl group optionally substituted by up to 3 fluorine, chlorine and/or bromine atoms; R2 is a hydrogen atom or a C1-6 straight-chain alkyl group; R3 is a hydrogen atom; a C1-10 alkyl group; a cyano group; an alkyl group substituted by one or more halogen atoms or by a hydroxy group, a cyano group, a C1-6 alkoxy group, an aryloxy group, a C1-6 alkylsulphonyl group, an arylsulphonyl group, an aralkylsuphonyl group, an azido group, a C1-6 alkoxycarbonyl group, an aralkoxycarbonyl group, a hydroxycarbonyl group, a phosphoryl group, a phosphoryloxy group, or an amine oxide, carbamoyl or thiocarbamoyl group in which each nitrogen is substituted by hydrogen or by 1 or 2 C1-4 alkyl groups; a C2-4 alkenyl or alkynyl group; an aryl or aralkyl group, each containing from 6 to 11 carbon atoms including 1 to 4 carbon atoms in the alkyl portion and optionally ring substituted by one or more fluorine, chlorine and/or bromine atoms or by a C1-2 alkyl or alkoxy group, each optionally substituted by one or more fluorine and/or chlorine atoms; a group -CSNH2; a group -CO2R8 or -CON(R8)2 in which R8 is a hydrogen atom or a C1-6 alkyl group; or a C1-6 acyl group or an oxime or an acetal derivative of said acyl group; each R4 is independently a hydrogen atom; an alkyl group optionally substituted by up to 3 halogen atoms; a hydroxy group; or a C1-4 alkoxy group; or one of R4 and R1 together form a carbon-carbon bond; R5 and R6 each independently is a hydrogen atom or a C alkyl group; or when located on a carbon atom adjacent to a the ring oxygen atom then R5 and R6 together form an alkylene group containing 4 or 5 carbon atoms; each R7 independently is a hydrogen atom or a C1-4 alkyl group optionally substituted by up to 3 halogen atoms; or when n is 0 then R7 is also a chlorine or bromine atom, or two of R7 when located on adjacent carbon atoms together form an epoxide ring or a carbon-carbon bond; or when n is 1, then one R7 on the carbon adjacent to the carbon bearing R2 is a hydroxy group a C7-11 aralkoxy group, or a C1-4 alkoxy group, and the other R7 is a hydrogen atom; both of Q are hydrogen atoms or fluorine atoms; and W is an optionally-substituted unsaturated group of up to 4 carbon atoms; an optionally substituted aryl or heterocyclic group containing up to 14 carbon atoms; a C3-10 cycloaliphatic group optionally substituted by C1-3 alkyl; or a C3-10 secondary alkyl group.
56 Entgegengehaltene Patentdokumente/Zitate,
in Recherche ermittelt
CT
56 Entgegengehaltene Patentdokumente/Zitate,
vom Anmelder genannt
CT
56 Entgegengehaltene Nichtpatentliteratur/Zitate,
in Recherche ermittelt
CTNP
56 Entgegengehaltene Nichtpatentliteratur/Zitate,
vom Anmelder genannt
CTNP
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Sequenzprotokoll
Prüfstoff-IPC ICP A01N 57/16
A01N 57/24
C07D 493/08
C07D 493/18
C07F 9/38