Abstract:
Substd. 2-phenyl-3-alkoxy-acrylate ester cpds. of formula (I) are new: n = 0-4; R = alkyl, alkenyl, alkynyl, etc.; or R+R on adjacent C = 3-4 membered bridge contg. 0-2 N, O and/or S, and the rest C (where the ring formed is opt. unsatd. or aromatic); R1, R2 = 1-4C alkyl; R3 = a pyrazolyl or triazolyl gp. of e.g. formula (a1): R4 = alkyl, alkenyl, alkynyl, etc.; Het = N, O or S; m = 0-2; R5 = CN, NO2, halo, etc..
Abstract:
PCT No. PCT/EP96/05523 Sec. 371 Date May 28, 1998 Sec. 102(e) Date May 28, 1998 PCT Filed Dec. 11, 1996 PCT Pub. No. WO97/21686 PCT Pub. Date Jun. 19, 19972-(O-[pyrimidin-4-yl]methylenoxy)phenylacetic acid derivatives of the general formula I and the salts and N-oxides thereof where the radicals R1 to R4 and Q have the following meanings: R1 is hydrogen or alkyl; R2 is halogen, alkyl or haloalkyl; R3 is hydrogen; amino; hydroxyl; mercapto; halogen; unsubstituted or phenyl-substituted alkyl; haloalkyl; alkoxyalkyl; alkoxy; monoalkylamino; dialkylamino; alkylthio; alkylsulfoxyl; alkylsulfonyl; cycloalkyl; trialkylsilyloxy, or: phenyl, phenoxy, phenoxymethyl, benzyloxy or hetaryl, unsubstituted or substituted in the aromatic ring; R4 is hydrogen; cyano; halogen; alkyl; haloalkyl or alkoxy; Q is C(=NOCH3)-CONHCH3, C(=NOCH3)-COOCH3 or N(OCH3)-COOCH3, the salts and N-oxides thereof, and their use for controlling harmful fungi and animal pests.
Abstract:
PCT No. PCT/EP95/01554 Sec. 371 Date Oct. 31, 1996 Sec. 102(e) Date Oct. 31, 1996 PCT Filed Apr. 25, 1995 PCT Pub. No. WO95/29896 PCT Pub. Date Nov. 9, 1995Methyl alpha -phenylbutenoates of the formula I I where +E,uns --+EE is a single or double bond and the index and the substituents have the following meanings: n is 0, 1, 2, 3 or 4; R1 is nitro, cyano, halogen, alkyl, haloalkyl or alkoxy; R2 is hydrogen, nitro, cyano, halogen, alkyl, haloalkyl, alkoxy, alkylthio or alkoxycarbonyl; R3 is unsubst. or subst. alkyl, alkenyl or alkynyl; an unsubst. or subst. saturated or mono-or diunsaturated ring which, in addition to carbon atoms, can contain one to three of the following heteroatoms as ring members: oxygen, sulfur and nitrogen, or an unsubst. or subst. mono- or binuclear aromatic radical which, in addition to carbon atoms, can contain one to four nitrogen atoms or one or two nitrogen atoms and an oxygen or sulfur atom or an oxygen or sulfur atom as ring members, processes for their preparation and their use are described.
Abstract:
PCT No. PCT/EP95/04375 Sec. 371 Date May 6, 1997 Sec. 102(e) Date May 6, 1997 PCT Filed Nov. 7, 1995 PCT Pub. No. WO96/16047 PCT Pub. Date May 30, 19962-[(2-Alkoxy-6-trifluoromethylpyrimidin-4-yl)oxymethylene]-phenylacetic acid derivatives of the formula I where the index and the substituents have the following meanings: U is CH or N; V is O or NH; R is alkyl; R1 is cyano, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy or phenyl; n is 0 or an integer from 1 to 4, processes and intermediates for their preparation, and their use are described.
Abstract:
Substituted 2-(2'-pyridyloxy)phenylacetamides I,whereR1 is fluorine, chlorine, CH3 or halomethyl;R2 is fluorine, bromine, alkyl or halomethyl;R3 is hydrogen or one of the radicals mentioned under R2; andR2 is 6-chloro if R3 is hydrogen,R3 is 5-chloro if R2 is fluorineand the compound in which R1, R2 and R3 are each chlorinewith the proviso that R1 may not be chlorine if R2 is 5-trifluoromethyl and R3 is hydrogen,and processes for their preparation and their use for controlling harmful fungi and animal pests are described.
Abstract:
The invention concerns phenylacetic acid derivatives of the above formula in which the substituents and the indices have the following meanings: X denotes NOCH3, CHOCH3 and CHCH3; Y denotes oxygen or NRa; Ra denotes hydrogen or alkyl R denotes cyano, nitro, trifluoromethyl, halogen, alkyl and alkoxy; m stands for 0, 1 or 2, wherein the radicals R can be different if m is 2; R1 denotes hydrogen or alkyl; R2 and R3, independently of each other, denote hydrogen, cyano, nitro, hydroxy, amino, halogen, optionally substituted alkyl, alkoxy, alkylthio, alkylamino, dialkylamino, alkenyl, alkenyloxy, alkenylthio, alkenylamino, N-alkenyl-N-alkylamino, alkynyl, alkynyloxy, alkynylthio, alkynylamino, N-alkynyl-N-alkylamino, cycloalkyl, cycloalkyloxy, cycloalkylthio, cycloalkylamino, N-cycloalkyl-N-alkylamino, cycloalkenyl, cycloalkenyloxy, cycloalkenylthio, cycloalkenylamino, N-cycloalkenyl-N-alkylamino, heterocyclyl, heterocyclyloxy, heterocyclylthio, heterocyclylamino, N-heterocyclyl-N-alkylamino, aryl, aryloxy, arylthio, arylamino, N-aryl-N-alkylamino, hetaryl, hetaryloxy, hetarylthio, hetarylamino and N-hetaryl-N-alkylamino; R4 denotes one of the groups mentioned in the case of R2 or a CRd=NORe group; Rd denotes one of the groups mentioned in the case of R2; and Re denotes hydrogen, optionally substituted alkyl, cycloalkyl, alkenyl, alkynyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, alkylsulphonyl, aryl, arylcarbonyl, arylsulphonyl, hetaryl, hetarylcarbonyl or hetarylsulphonyl. The invention also concerns their salts, a process for the preparation of these substances and their use.