Abstract:
PROBLEM TO BE SOLVED: To obtain the subject compound of which oxide content is decreased by adding a metal salt to form a complex thereof with trisubstituted phosphine and separating the complex formed from the mixture. SOLUTION: A reducing agent such as a trisubstituted phosphine represented by the formula (R is H, a 1-6C alkyl; R and R are each H, a 1-6C alkyl; R and R are each H, a 1-6C alkyl; R -R are each H, a 1-6C haloalkyl) is oxidized to form the oxide. A metal salt of an alkali metal is added to the oxide in a range from 0.25-5 molar equivalent based on the oxide to effect the Mitsunobu reaction. In the reaction, the reaction mixture is kept at the temperature ranging from 0 to 120 deg.C for 16 hours at maximum, then cooled down in the temperature range from -10 deg.C - the ambient temperature to form complex. The remaining complex is separated by filtration or centrifugation to decrease the oxide.
Abstract:
A substituted 2-phenylpyridine of formula (I), where Ar is a radical (A) or (B) and where the ring R is a fused heterocyclic ring which, together with the phenyl ring, forms one of the following bicyclic rings (a) to (l) and the N-oxides of (I) and the agriculturally utilizable salts of (I) if these exist. Use: herbicides, desiccation/defoliation of plants.
Abstract:
The invention relates to a method for producing N-acylated (hetero)aromati c hydroxylamine derivatives of formula (I), wherein the substituents, the ring atom and the index have the meanings given in the Description, by hydrogenating a (hetero)aromatic nitro-compound of general formula (II) in the presence of a hydrogenation catalyst.
Abstract:
The invention relates to a method for producing N-acylated (hetero)aromatic hydroxylamine derivatives of formula (I), wherein the substituents, the ring atom and the index have the meanings give in the Description, by hydrogenating a (hetero)aromatic nitro-compound of general formula (II) in the presence of a hydrogenation catalyst.
Abstract:
PCT No. PCT/EP94/02264 Sec. 371 Date Jan. 11, 1996 Sec. 102(e) Date Jan. 11, 1996 PCT Filed Jul. 11, 1994 PCT Pub. No. WO95/02590 PCT Pub. Date Jan. 26, 1995A substituted 2-phenylpyridine of the formula I where Ar is and the N-oxides of I and the agriculturally utilizable salts of I where these exist. Use: herbicides; desiccation/defoliation of plants.
Abstract:
PCT No. PCT/EP98/04490 Sec. 371 Date Jan. 27, 2000 Sec. 102(e) Date Jan. 27, 2000 PCT Filed Jul. 20, 1998 PCT Pub. No. WO99/06373 PCT Pub. Date Feb. 11, 19992-(3-Pyrazolyloxymethylene)nitrobenzene [sic] derivatives of the formula I where the substituents and indices have the meanings given in the description, are prepared by bromination of an o-nitrotoluene of the formula II and subsequent reaction with a 3-hydroxypyrazole of the formula IV
Abstract:
PCT No. PCT/EP97/06780 Sec. 371 Date Jun. 14, 1999 Sec. 102(e) Date Jun. 14, 1999 PCT Filed Dec. 4, 1997 PCT Pub. No. WO98/27062 PCT Pub. Date Jun. 25, 1998A process is described for preparing N-substituted 3-hydroxypyrazoles of the formula I where R1 is unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, aryl or heteroaryl and R2, R3 are hydrogen, cyano, halogen and unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, aryl or heteroaryl, by oxidizing a corresponding pyrazolidin-3-one.
Abstract:
PCT No. PCT/EP95/03286 Sec. 371 Date Feb. 18, 1997 Sec. 102(e) Date Feb. 18, 1997 PCT Filed Aug. 18, 1995 PCT Pub. No. WO96/06830 PCT Pub. Date Mar. 7, 1996N-Phenyltetrahydroindazoles of formula (I), where R1 is H or C1-4-alkyl; R2 is halogen, C1-4-alkyl or C1-4-haloalkyl; R3 is H or halogen; R4 is NO2, halogen, C1-4-alkyl or C1-4-haloalkyl; R5 is -XR6; X is -O-, -S-, -SO- or -SO2-; R6 is -Alk-R7; Alk is a substituted or unsubstituted methylene, ethylene, propylene, butylene or pentamethylene chain, where one chain member can carry a spiro-linked 2- to 5-membered C chain or where 2 ring members can be bridged via a C1-5-alkylene chain; R7 is CN, SCN, halogen or -YR11, where Y is -O-, -S-, -SO- or -SO2-; R10 is H, OH, C1-C4-alkyl, C1-C4-haloalkyl, C3-C5-cycloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C3-C5-cycloalkoxy, C1-C4-alkylthio, C1-C4-haloalkylthio, -NH-R12, -N(C1-C4-alkyl)-R12, -N(C3-C4-alkenyl)-R12, -N(C3-C4-alkynyl)-R12, pyrrolidin-1-yl, piperid-1-yl, morpholin-4-yl, azepan-1-yl, (i) unsubstituted or substituted phenyl, benzyl, phenoxy or benzyloxy; R11 is C1-6-alkyl, C1-6-haloalkyl or C1-6-cycloalkyl; R12 is H, OH, C1-4-alkyl, C3-4-alkenyl, C3-4-alkynyl, C3-6-cycloalkyl, C1-4-alkoxy, C3-4-alkenyloxy, C3-4-alkenyloxy, C3-4-alkynyloxy, or substituted or unsubstituted phenyl or benzyl; and the agriculturally utilizable salts of formula (I), with the provisoes that the simultaneous meaning of R6 as dihalomethyl, R2 and R4 as chlorine and R3 as halogen is excluded; the simultaneous meaning of X as oxygen and R7 as -OR11 or C1-C6-alkylthio is excluded; Alk must not carry a spiro-linked three-membered ring if R7 is halogen and R11 is not C1-6-alkyl if R1 is H, R2 is C1-4-haloalkyl, R3 is F, R4 is halogen and R7 is -R11. Use: as herbicides; for desiccating/defoliating plants.