(EP1171437) A compound of formula (I) wherein G is either (i) or (ii), where M<1> or M<2> is bonded to A; n is 0 or 1; when G is (i), D is S, NR<7>, CR<8>=CR<9>, CR<8>=N, CR<8>=N(O), N=CR<9> or N(O)=CR<9>; when G is (ii), D is S or NR<7>; E is N, N-oxide or CR<10>; M<1> is OC(=Y), N(R<11>)C(=Y), N=C(OR<12>), N=C(SR<13>) or N=C(NR<14>R<15>) where O or N is the atom of attachment to the ring containing D and E; M<2> is N-C(=Y) where N is the atom of attachment to the ring containing D and E; Y is O, S or NR<16>; J is N or CR<17>; and A, R<1>, R<2>, R<3>, R<4>, R<5>, R<6>, R<7>, R<8>, R<9>, R<10>, R<11>, R<12>, R<13>, R<14> and R<15> are each certain organic or inorganic groups. These compounds are useful in fungicidal, insecticidal, acaricidal, molluscicidal and hematicidal compositions.
(EP1171437) 1. A compound of formula (I): (see diagramm 1 page 111) wherein G is either (see diagramm 2 page 111) where M**1 or M**2 is bonded to A; n is 0 or 1; A is optionally substituted C1-6 alkylene, optionally substituted C2-6 alkenylene, optionally substituted C2-6 alkynylene, optionally substituted C1-6 alkylenoxy, optionally substituted oxy(C1-6 )alkylene, optionally substituted C1-6 alkylenethio, optionally substituted thio(C1-6 )alkylene, optionally substituted C1-6 alkylenamino, optionally substituted amino(C1-6 )alkylene, optionally substituted [C1-6 alkyleneoxy(C1-6 )alkylene], optionally substituted - [C1-6 alkylenethio(C1-6 )alkylene], optionally substituted [C1-6 alkylenesulfinyl(C1-6 )alkylene], optionally substituted [C1-6 alkylenesulfonyl(C1-6 )alkylene] or optionally substituted [C1-6 alkyleneamino(C1-6 )alkylene]; when G is (i), D is S, NR**7 , CR**8 =CR**9 , CR**8 =N, CR**8 =N(O), N=CR**9 or N(O)=CR**9 ; when G is (ii), D is S or NR**7 ; E is N, N-oxide or CR**10 ; M**1 is OC(=Y), N(R**11 )C(=Y), N=C(OR**12 ), N=C(SR**13 ) or N=C(NR**14 R**15 ) where O or N is the atom of attachment to the ring containing D and E; M**2 is N-C(=Y) where N is the atom of attachment to the ring containing D and E; Y is O, S or NR**16 ; J is N or CR**17 ; R**1 is hydrogen, halogen, optionally substituted C1-6 alkyl, optionally substituted C2-6 alkenyl, optionally substituted C2-6 alkynyl, optionally substituted C1-6 alkoxy, optionally substituted C1-6 alkylthio, optionally substituted C3-7 cycloalkyl, cyano, nitro or SF5 ; R**2 is optionally substituted C1-10 alkyl, optionally substituted [C2-6 alkenyl(C1-6 )alkyl], optionally substituted [C2-6 alkynyl(C1-6 )alkyl], optionally substituted C3-7 cycloalkyl, optionally substituted C1-10 alkylcarbonyl, optionally substituted C1-10 alkoxycarbonyl, formyl, optionally substituted C1-10 alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl, optionally substituted phenoxycarbonyl, optionally substituted C1-6 alkylthio, optionally substituted C1-6 alkylsulfinyl, optionally substituted C1-6 alkylsulfonyl, optionally substituted arylthio, optionally substituted arylsulfinyl, optionally substituted arylsulfonyl or R**18 R**19 NS; R**3 , R**4 and R**5 are, independently, hydrogen, halogen, optionally substituted C1-6 alkyl, optionally substituted C1-6 alkoxy, optionally substituted C1-6 alkylthio, optionally substituted C1-6 alkylsulfinyl, optionally substituted C1-6 alkylsulfonyl, cyano, nitro, optionally substituted C1-6 alkylcarbonyl, optionally substituted C1-6 alkoxycarbonyl or SF5 ; R**6 is hydrogen, cyano, optionally substituted C1-20 alkyl, optionally substituted C2-20 alkenyl(C1-6 )alkyl, optionally substituted C2-20 alkynyl(C1-6 )alkyl, optionally substituted C3-7 cycloalkyl, optionally substituted C5-6 cycloalkenyl, formyl, optionally substituted C1-20 alkoxycarbonyl, optionally substituted C1-20 alkylcarbonyl, aminocarbonyl, optionally substituted C1-20 alkylaminocarbonyl, optionally substituted di(C1-20 )alkylaminocarbonyl, optionally substituted aryloxycarbonyl, optionally substituted arylcarbonyl, optionally substituted arylaminocarbonyl, optionally substituted N-alkyl-N-arylaminocarbonyl, optionally substituted diarylaminocarbonyl, optionally substituted heteroaryloxycarbonyl, optionally substituted heteroarylcarbonyl, optionally substituted heteroarylaminocarbonyl, optionally substituted alkylheteroarylaminocarbonyl, optionally substituted diheteroarylaminocarbonyl, optionally substituted phenyl, optionally substituted heteroaryl, optionally substituted heterocyclyl, optionally substituted C1-20 alkylsulfonyl or optionally substituted arylsulfonyl; R**7 is C1-6 alkyl; R**8 and R**9 are, independently, hydrogen, halogen, cyano, nitro, optionally substituted C1-6 alkyl, optionally substituted C2-6 alkenyl, optionally substituted C2-6 alkynyl or optionally substituted C1-6 alkoxy; R**10 is hydrogen, halogen, optionally substituted C1-6 alkyl, optionally substituted C2-6 alkenyl, optionally substituted C2-6 alkynyl, optionally substituted C1-6 alkoxy, optionally substituted C1-6 alkylthio, optionally substituted - C1-6 alkylsulfinyl, optionally substituted C1-6 alkylsulfonyl, cyano, nitro, formyl, R**20 ON=C(R**21 ), optionally substituted C1-6 alkylcarbonyl, optionally substituted C1-6 alkoxycarbonyl or SF5 ; or R**1 and R**10 together with the atoms to which they are attached may be joined to form a five, six or seven-membered saturated or unsaturated ring carbocylic or heterocyclic ring which may contain one or two hetero atoms selected from O, N and S and which may be optionally substituted by C1-6 alkyl, C1-6 haloalkyl or halogen; R**11 is hydrogen, optionally substituted C1-10 alkyl, optionally substituted [C2-6 alkenyl(C1-6 )alkyl], optionally substituted [C2-6 alkynyl(C1-6 )alkyl], optionally substituted C3-7 cycloalkyl, optionally substituted C1-10 alkylcarbonyl, optionally substituted C1-10 alkoxycarbonyl, formyl, optionally substituted C1-10 alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl, optionally substituted phenoxycarbonyl, optionally substituted C1-6 alkylthio, optionally substituted C1-6 alkylsulfinyl, optionally substituted C1-6 alkylsulfonyl, optionally substituted arylthio, optionally substituted arylsulfinyl, optionally substituted arylsulfonyl or R**22 R**23 NS; R**12 is optionally substituted C1-10 alkyl, optionally substituted [C2-6 alkenyl(C1-6 )alkyl], optionally substituted [C2-6 alkynyl(C1-6 )alkyl], optionally substituted C3-7 cycloalkyl, optionally substituted C1-10 alkylcarbonyl, optionally substituted C1-10 alkoxycarbonyl, formyl, optionally substituted C1-10 alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl, , amino, optionally substituted C1-6 alkylamino, optionally substituted di(C1-6 )alkylamino, optionally substituted phenoxycarbonyl, tri(C1-4 )alkylsilyl, aryldi(C1-4 )alkylsilyl, (C1-4 )alkyldiarylsilyl or triarylsilyl; R**13 is optionally substituted C1-10 alkyl, optionally substituted [C2-6 alkenyl(C1-6 )alkyl], optionally substituted [C2-6 alkynyl(C1-6 )alkyl], optionally substituted C3-7 cycloalkyl, optionally substituted C1-10 alkylcarbonyl, optionally substituted C1-10 alkoxycarbonyl, optionally substituted C1-10 alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl or optionally substituted phenoxycarbonyl); R**14 and R**15 are, independently optionally substituted C1-10 alkyl, optionally substituted C1-6 alkoxy, optionally substituted [C2-6 alkenyl(C1-6 )alkyl], optionally substituted [C2-6 alkynyl(C1-6 )alkyl], optionally substituted C3-7 cycloalkyl, optionally substituted C1-10 alkylcarbonyl, optionally substituted C1-10 alkoxycarbonyl, formyl, optionally substituted C1-10 alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl, hydroxy, amino, optionally substituted C1-6 alkylamino, optionally substituted di(C1-6 )alkylamino, or optionally substituted phenoxycarbonyl; R**16 is hydrogen, cyano, nitro, optionally substituted C1-6 alkyl, optionally substituted C3-7 cycloalkyl, optionally substituted (C2-6 )alkenyl(C1-6 )alkyl, optionally substituted (C2-6 )alkynyl(C1-6 )alkyl, optionally substituted phenyl, optionally substituted heteroaryl, optionally substituted C1-6 alkylcarbonyl, optionally substituted C1-6 alkoxycarbonyl, optionally substituted C1-6 alkylamino, optionally substituted di(C1-6 )alkylamino, optionally substituted C1-6 alkylcarbonylamino, optionally substituted C1-6 alkoxycarbonylamino, optionally substituted C1-6 alkoxy, optionally substituted C1-6 alkylthio, optionally substituted C1-6 alkylsulfinyl, optionally substituted C1-6 alkylsulfonyl, optionally substituted arylthio, optionally substituted arylsulfinyl, optionally substituted arylsulfonyl or C1-6 acyloxy; R**17 is hydrogen, halogen, nitro, cyano, optionally substituted C1-8 alkyl, optionally substituted C2-6 alkenyl, optionally substituted C2-6 alkynyl, optionally substituted C3-7 cycloalkyl, optionally substituted C1-6 alkoxycarbonyl, optionally substituted C1-6 alkylcarbonyl, optionally substituted C1-6 alkylaminocarbonyl, optionally substituted di(C1-6 )alkylaminocarbonyl, optionally substituted phenyl or optionally substituted heteroaryl; R**18 and R**19 are, independently, optionally substituted C1-6 alkyl or R**18 and R**19 together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selected from O, N or S and which may be optionally substituted by one or two C1-6 alkyl groups; R**20 is hydrogen, optionally substituted phenyl, optionally substituted phenyl(C1-4 )alkyl or optionally substituted C1-20 alkyl; R**21 is hydrogen, optionally substituted phenyl or optionally substituted C1-6 alkyl; and R**22 and R**23 are, independently, optionally substituted C1-6 alkyl or R**22 and R**23 together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selected from O, N or S and which may be optionally substituted by one or two C1-6 alkyl groups; wherein the optional substituents, when present, on the alkylene, alkenylene or alkynylene moieties are, subject to valency constraints, one or more of halogen, C1-6 alkyl, C1-6 haloalkyl, C1-6 cyanoalkyl, C1-6 alkoxy(C1-6 ) alkyl, C1-6 alkoxy, cyano, =O, =NR**24 and =CR**25 R**26 , wherein R**24 is C1-6 alkyl, C1-6 haloalkyl, OR**27 or R**28 R**29 N; where R**25 and R**26 are, independently, hydrogen, C1-6 alkyl, C1-6 alkoxy, C1-6 haloalkyl, cyano, C1-6 alkoxycarbonyl, C1-6 alkylcarbonyl or R**30 R**31 N; R**27 is C1-6 alkyl, C1-6 haloalkyl or phenyl(C1-2 )alkyl; R**28 and R**29 are, independently, hydrogen, C1-8 alkyl, C3-7 cycloalkyl, C2-6 alkenyl(C1-6 )alkyl, C2-6 alkynyl(C1-6 )alkyl, C2-6 haloalkyl, C1-6 alkoxy(C1-6 )alkyl, C1-6 alkoxycarbonyl(C1-6 )alkyl, carboxy(C1-6 )alkyl or phenyl(C1-2 )alkyl or R**28 and R**29 together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selected from O, N or S and which may be optionally substituted by one or two C1-6 alkyl groups; R**30 and R**31 are, independently, hydrogen, C1-8 alkyl, C3-7 cycloalkyl, C2-6 alkenyl(C1-6 )alkyl, C2-6 alkynyl(C1-6 )alkyl, C2-6 haloalkyl, C1-6 alkoxy-(C1-6 )alkyl, C1-6 alkoxycarbonyl(C1-6 )alkyl, carboxy(C1-6 )alkyl or phenyl(C1-2 )alkyl; or R**30 and R**31 together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selectedfrom O, N or S and which may be optionally substituted by one or two C1-6 alkyl groups; and wherein each alkyl moiety is a straight or branched chain and, when present, the optional substituents on alkyl are one or more of halogen, nitro, cyano, HO2 C, C1-10 alkoxy (itself optionally substituted by C1-10 alkoxy), aryl-(C1-4 )alkoxy, C1-10 alkylthio, C1-10 alkylcarbonyl, C1-10 alkoxycarbonyl, C1-6 alkylaminocarbonyl, di(C1-6 alkyl)aminocarbonyl, (C1-6 )alkylcarbonyloxy, optionally substituted phenyl, heteroaryl, aryloxy, arylcarbonyloxy, heteroaryloxy, heterocyclyl, heterocyclyloxy, C3-7 cycloalkyl (itself optionally substituted with (C1-6 )alkyl or halogen), C3-7 cycloalkyloxy, C5-7 cycloalkenyl, C1-6 alkylsulfonyl, C1-6 alkylsulfinyl, tri(C1-4 )alkylsilyl, tri(C1-4 )alkylsilyl-(C1-6 )alkoxy, aryldi(C1-4 )alkylsilyl, (C1-4 )alkyldiarylsilyl, triarylsilyl, =N-OR' and =N-NR'R"; where R' and R" are, independently, C1-6 alkyl or C1-6 haloalkyl; and where the alkenyl and alkynyl moieties are in the form of straight or branched chains, and the alkenyl moieties, where appropriate, can be of either the (E)- or (Z)-configuration; and, when present, the optional substituents on alkenyl or alkynyl are one or more of halogen, aryl and C3-7 cycloalkyl; and wherein acyl is optionally substituted C1-6 alkylcarbonyl, optionally substituted C2-6 alkenylcarbonyl, optionally substituted C2-6 alkynylcarbonyl, optionally substituted arylcarbonyl or optionally substituted heteroarylcarbonyl; and wherein halogen is fluorine, chlorine, bromine or iodine; haloalkyl groups are alkyl groups which are optionally substituted with one or more of the same or different halogen atoms; aryl is phenyl, naphthyl, anthracyl, fluorenyl and indenyl; heteroaryl is an aromatic ring containing up to 10 atoms including one or more heteroatoms selected from O, S and N; heterocycle and heterocyclyl are a non-aromatic ring containing up to 10 atoms including one or more heteroatoms selected from O, S and N; cycloalkyl is cyclopropyl, cyclopentyl and cyclohexyl and the optional substituents for cycloalkyl are halogen, cyano and C1-3 alkyl; cycloalkenyl is cyclopentenyl and cyclohexenyl and the optional substituents for cycloalkenyl are C1-3 alkyl, halogen and cyano; carbocyclic rings are aryl, cycloalkyl and cycloalkenyl groups; and for substituted phenyl moieties, heterocyclyl and heteroaryl groups the substituents are independently selected from one or more of halogen, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy(C1-6 )alkyl, C1-6 alkoxy, C1-6 haloalkoxy, C1-6 alkylthio, C1-6 haloalkylthio, C1-6 alkylsulfinyl, C1-6 haloalkylsulfinyl, C1-6 alkylsulfonyl, C1-6 haloalkylsulfonyl, C2-6 alkenyl, C2-6 haloalkenyl, C2-6 alkynyl, C3-7 cycloalkyl, nitro, cyano, CO2 H, C1-6 alkylcarbonyl, C1-6 alkoxycarbonyl, R**32 R**33 N or R**34 R**35 NC(O) wherein R**32 , R**33 , R**34 and R**35 are, independently, hydrogen or C1-6 alkyl; and wherein dialkylamino substituents include those where the dialkyl groups together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selected from O, N or S and which may be optionally substituted by one or two C1-6 alkyl groups; and when heterocyclic rings are formed by joining two groups on an N atom, the resulting rings are pyrrolidine, piperidine, thiomorpholine and morpholine each of which may be substituted by one or two (C1-6 )alkyl groups. 2. A compound as claimed in claim 1 of formula (IA): (see diagramm 1 page 117) wherein A, G, J, R**3 , R**4 , R**5 and R**6 are as claimed in claim 1. 3. A compound of formula (I) as claimed in claim 1 or a compound of formula (IA) as claimed in claim 2 wherein, when G is (i) as defined in claim 1, D is S or CR**8 =CR**9 , where R**8 and R**9 are, independently, hydrogen, halogen, C1-6 alkyl, C1-6 haloalkyl C2-6 alkenyl, C2-6 alkynyl, C1-6 alkoxy or C1-6 haloalkoxy; when G is (ii) as defined in claim 1, D is S; E is N or CR**10 where R**10 is hydrogen, halogen, C1-6 alkyl, C1-6 haloalkyl, - C1-6 alkoxy, C1-6 haloalkoxy, C1-6 alkoxy (C1-6 )alkyl, C1-6 alkylthio or SF5 ; or R**1 and R**10 together with the atoms to which they are attached form a benzene ring optionally substituted by C1-6 alkyl, C1-6 haloalkyl or halogen; and M**1 is N(R**11 )C(=O) where R**11 is hydrogen, C1-6 alkyl, C1-6 alkoxy(C1-6 )alkyl, benzyloxymethyl or benzoyloxymethyl. 4. A compound of formula (I) as claimed in claim 1 or 3 or a compound of formula (IA) as claimed in claim 2 or 3 wherein A is C1-4 alkylene, -C(O)- or C1-4 alkyleneoxy. 5. A compound of formula (I) as claimed in claim 1, 3 or 4 or a compound of formula (IA) as claimed in claim 2, 3 or 4 wherein G is (i) as defined in claim 1 and n is 0. 6. A compound of formula (I) as claimed in claim 1, 3, 4 or 5 or a compound of formula (IA) as claimed in claim 2, 3, 4 or 5 wherein R**3 , R**4 and R**5 are, independently, hydrogen, C1-3 alkyl or halogen. 7. A compound of formula (I) as claimed in claim 1, 3, 4, 5 or 6 or a compound of formula (IA) as claimed in claim 2, 3, 4, 5 or 6 wherein R**6 is C1-10 alkyl or C1-10 haloalkyl (each one of which may be substituted with a C1-6 alkyloxime, C1-6 haloalkyloxime, C1-6 alkylhydrazone or C1-6 haloalkylhydrazone group) or C1-6 cyanoalkyl, C2-6 alkenyl(C1-6 )alkyl, C2-6 alkynyl(C1-6 )alkyl, C3-7 cycloalkyl, C3-7 halocycloalkyl, C3-7 cyanocycloalkyl, C1-3 alkyl(C3-7 )cycloalkyl, C1-3 alkyl(C3-7 )halocycloalkyl, C5-6 cycloalkenyl, C3-7 cycloalkyl(C1-6 )alkyl, C5-6 cycloalkenyl(C1-6 )alkyl, C2-6 haloalkenyl(C1-6 )alkyl, C1-6 cyanoalkenyl(C1-6 )alkyl, C1-6 alkoxy(C1-6 )alkyl, C3-6 alkenyloxy(C1-6 )alkyl, C3-6 alkynyloxy(C1-6 )alkyl, aryloxy(C1-6 )alkyl, C1-6 carboxyalkyl, C1-6 alkylcarbonyl(C1-6 )alkyl, C2-6 alkenylcarbonyl(C1-6 )alkyl, C2-6 alkynylcarbonyl(C1-6 )alkyl, C1-6 alkoxycarbonyl(C1-6 )alkyl, C3-6 alkenyloxycarbonyl(C1-6 )alkyl, C3-6 alkynyloxycarbonyl(C1-6 )alkyl, aryloxycarbonyl(C1-6 )alkyl, C1-6 alkylthio(C1-6 )alkyl, C1-6 alkylsulfinyl(C1-6 )alkyl, C1-6 alkylsulfonyl(C1-6 )alkyl, aminocarbonyl(C1-6 )alkyl, aminocarbonyl(C2-6 )alkenyl, aminocarbonyl(C2-6 )alkynyl, C1-6 alkylaminocarbonyl(C1-6 )alkyl, di(C1-6 )alkylaminocarbonyl(C1-6 )alkyl, C1-6 alkylaminocarbonyl(C2-6 )alkenyl(C1-6 )alkyl, di(C1-6 )alkylaminocarbonyl(C2-6 )alkenyl(C1-6 )alkyl, alkylaminocarbonyl(C2-6 )alkynyl(C1-6 )alkyl, di(C1-6 )alkylaminocarbonyl(C2-6 )alkynyl(C1-6 )alkyl, phenyl (optionally substituted by halo, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy or C1-6 haloalkoxy), phenyl(C1-4 )alkyl (wherein the phenyl group is optionally substituted by halo, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy or C1-6 haloalkoxy), phenyl(C2-4 )alkenyl(C1-6 )alkyl, (wherein the phenyl group is optionally substituted by halo, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 alkylsulfonyl or C1-6 haloalkoxy), heteroaryl (optionally substituted by halo, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy or C1-6 haloalkoxy), heterocyclyl (wherein the heterocyclyl group is optionally substituted by halo, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy or C1-6 haloalkoxy), heteroaryl(C1-4 )alkyl (wherein the heteroaryl group is optionally substituted by halo, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy, C1-6 alkylsulfonyl or C1-6 haloalkoxy)or heterocyclyl(C1-4 )alkyl (wherein the heterocyclyl group is optionally substituted by halo, nitro, cyano, C1-6 alkyl, C1-6 haloalkyl, C1-6 alkoxy or C1-6 haloalkoxy). 8. A compound of formula (I) as claimed in claim 1, 3, 4, 5, 6 or 7 or a compound of formula (IA) as claimed in claim 2, 3, 4, 5, 6 or 7 wherein J is N or CR**17 where R**17 is hydrogen, C1-6 alkyl, C1-6 haloalkyl, cyano, halogen or nitro. 9. A process for preparing a compound of formula (I) as claimed in claim 1 comprising (a) where Y is oxygen, reacting a compound of formula (II) (see diagramm 1 page 119) where D, E, R**1 and R**11 are as defined in claim 1 with a compound of formula (III) (see diagramm 2 page 119) where Y is oxygen, X**1 is a leaving group and A, J, R**3 , R**4 , R**5 and R**6 are as defined in claim 1; or (b) where Y is sulphur, preparing a compound of formula (I) as claimed in claim 1 where Y is oxygen using the method described in (a) and then reacting this compound with a thionating agent. 10. A fungicidal, insecticidal, acaricidal, molluscicidal or nematicidal composition comprising a fungicidally, insecticidally, acaricidally, molluscicidally or nematicidally effective amount of a compound of formula (I) as claimed in claim 1 and a carrier or diluent therefor. 11. A method of combating and controlling fungi comprising applying to a plant, to a seed of a plant, to the locus of the plant or seed or to the soil a fungicidally effective amount of either a compound of formula (I) as claimed in claim 1. 12. A method of combating and controlling insects, acarines, nematodes or molluscs which comprises applying to a pest, to a locus of a pest, or to a plant susceptible to attack by a pest an insecticidally, acaricidally, nematicidally or molluscicidally effective amount of a compound of formula (I) as claimed in claim 1.
(EP1171437) LEGAL DETAILS FOR EP1171437 Actual or expected expiration date=2011-07-14 Legal state=DEAD Status=LAPSED Event publication date=2000-04-04 Event code=EP/APP Event indicator=Pos Event type=Examination events Application details Application country=EP EP00919009 Application date=2000-04-04 Standardized application number=2000EP-0919009 Event publication date=2002-01-16 Event code=EP/A1 Event type=Examination events Application published with search report Publication country=EP Publication number=EP1171437 Publication stage Code=A1 Publication date=2002-01-16 Standardized publication number=EP1171437 Event publication date=2002-01-16 Event code=EP/AK Event indicator=Pos Event type=Designated states Designated contracting states: Benannte vertragsstaaten AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE Event publication date=2002-01-16 Event code=EP/17P Event indicator=Pos Event type=Examination events Request for examination filed Pruefungsantrag gestellt Effective date of the event=2001-11-20 Event publication date=2002-01-16 Event code=EP/AX Event indicator=Pos Event type=Designated states Extension of the European patent to Request for extension of the european patent to AL PAYMENT 20011120 LT PAYMENT 20011120 LV PAYMENT 20011120 MK PAYMENT 20011120 RO SI PAYMENT 20011120 Event publication date=2002-03-20 Event code=EP/17Q Event indicator=Pos Event type=Examination events First examination report Erster pruefungsbescheid Effective date of the event=2002-02-04 Event publication date=2002-09-18 Event code=EP/RAP1 Event type=Change of name or address Event type=Reassignment Transfer of rights of an application Anmelder uebertragung (korr.) 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