-
公开(公告)号:AU5334396A
公开(公告)日:1996-10-30
申请号:AU5334396
申请日:1996-03-25
Applicant: BASF AG
Inventor: MULLER RUTH , REMY BENOIT , BAYER HERBERT , GOTZ NORBERT , SAUTER HUBERT
IPC: C07D231/12 , C07B61/00 , C07C249/04 , C07C249/12 , C07C249/14 , C07C251/38 , C07C251/48 , C07C255/62 , C07D261/08
Abstract: PCT No. PCT/EP96/01306 Sec. 371 Date Oct. 7, 1997 Sec. 102(e) Date Oct. 7, 1997 PCT Filed Mar. 25, 1996 PCT Pub. No. WO96/32373 PCT Pub. Date Oct. 17, 1996A process for the preparation of largely isomerically pure alpha -bisoximes of the formula IaR1O-N=CR2-CR3=N-OR4Iawhere the groups R1O- and R2 on the N=C bond are cis to one another and where the radicals have the following meanings: R1 and R4 are hydrogen or a C-organic radical; R2 is hydrogen, cyano, nitro, hydroxyl, amino, halogen or an organic radical which can be bonded to the structure directly or via an oxygen, sulfur or nitrogen atom; R3 is hydrogen, cyano, nitro, hydroxyl, amino, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio, alkylamino, dialkylamino or cycloalkyl, from a mixture of the isomers of the a-bisoximes Ia and Ib is described.
-
公开(公告)号:AU5100596A
公开(公告)日:1996-10-02
申请号:AU5100596
申请日:1996-03-01
Applicant: BASF AG
Inventor: KLINTZ RALF , GOTZ NORBERT , SCHAFER PETER , HAMPRECHT GERHARD , HEISTRACHER ELISABETH , BUSSCHE-HUNNEFELD CHRISTOPH-SW , HARREUS ALBRECHT , WESTPHALEN KARL-OTTO , WALTER HELMUT , MISSLITZ ULF
IPC: C07D239/54 , A01N43/60 , A01N43/84 , C07D241/52 , C07D241/54 , C07D265/36 , C07D403/04 , C07D413/04
Abstract: 3-Aryluracils of the formula IwhereinA is hydrogen, methyl or amino;X is oxygen or -N(R7)- (R7=H alkyl, alkenyl, alkynyl, alkylcarbonyl or alkoxyalkyl);Y1 is oxygen or sulfur;Z is oxygen or -N(R8)- (R8=H, alkyl, alkenyl, alkynyl or alkoxyalkyl);R1 is hydrogen or halogen;R2 is hydrogen, halogen, alkyl, haloalkyl, alkylthio, alkylsulfenyl or alkylsulfonyl;R3 is hydrogen, halogen or alkyl;R4 is hydrogen; or optionally substituted alkyl, cycloalkyl, haloalkyl, alkenyl, alkynyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl or alkylsulfonyl,R5, R6 are hydrogen, alkyl, alkenyl, alkynyl or alkoxyalkyl; orR6, R8 are together a second chemical bond, methods and intermediates for their manufacture, and their use as herbicides or for the desiccation or defoliation of plants.
-
公开(公告)号:AU4621596A
公开(公告)日:1996-08-27
申请号:AU4621596
申请日:1996-01-26
Applicant: BASF AG
Inventor: KLINTZ RALF , SCHAFER PETER , HAMPRECHT GERHARD , HEISTRACHER ELISABETH , BUSSCHE-HUNNEFELD CHRISTOPH-SW , GOTZ NORBERT , HARREUS ALBRECHT , WESTPHALEN KARL-OTTO , WALTER HELMUT , MISSLITZ ULF
IPC: A01N25/02 , A01N25/08 , A01N25/12 , A01N25/34 , A01N43/54 , C07C237/18 , C07C255/59 , C07C255/60 , C07C275/42 , C07D239/54 , C07D239/56
-
204.
公开(公告)号:NZ272044A
公开(公告)日:1996-01-26
申请号:NZ27204495
申请日:1995-05-02
Applicant: BASF AG
Inventor: KONIG HARTMANN , GOTZ NORBERT , KIRSTGEN REINHARD , MULLER BERND , OBERDORF KLAUS
IPC: C07D231/22 , C07D231/18 , C07D401/04 , C07D403/04
Abstract: The prepn. of 1-(Hetero)aryl-3-hydroxy-pyrazoles of formula (I) comprises mixing propiolic acid esters of formula R1C IDENTICAL CCOOR' (II) with (hetero)arylhydrazine derivs. of formula RNHNH2 (III) in an inert solvent; and then treating with a base at 0-60 degrees C. R = opt. substd. aromatic or heteroaromatic; n = 0, 1 or 2; R1 = a gp. which is stable under the reaction conditions; R' = alkyl, cycloalkyl or aryl.
-
公开(公告)号:NZ560916A
公开(公告)日:2010-12-24
申请号:NZ56091606
申请日:2006-03-15
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS , RHEINHEIMER JOACHIM , LOHMANN JAN KLAAS , GROTE THOMAS , PUHL MICHAEL , KORADIN CHRISTOPHER , BAUMANN ERNST , VON DEYN WOLFGANG , LANGEWALD JURGEN , GOTZ NORBERT , CULBERTSON DEBORAH L , ANSPAUGH DOUGLAS D , OLOUMI-SADEGHI HASSAN , COTTER HENRY VAN TUYL , KUHN DAVID G
IPC: A01N43/40 , C07D213/42
Abstract: Disclosed are biphenylsulfonamides of formula I wherein the substituents are disclosed within the specification. Also disclosed are processes for preparing the compounds of formula I. Also disclosed is the use of the compound of formula I for the treatment of phytopathogenic harmful fungi and for combating harmful anthropodes.
-
206.
公开(公告)号:SK287476B6
公开(公告)日:2010-11-08
申请号:SK16872000
申请日:1999-05-04
Applicant: BASF AG
Inventor: RHEINHEIMER JOACHIM , VON DEYN WOLFGANG , GEBHARDT JOACHIM , RACK MICHAEL , LOCHTMAN RENE , GOTZ NORBERT , KEIL MICHAEL , WITSCHEL MATTHIAS , HAGEN HELMUT , MISSLITZ ULF , BAUMANN ERNST
IPC: C07C205/00 , C07C20060101 , C07C201/00 , C07C201/12 , C07C205/44 , C07C249/00 , C07C249/06 , C07C251/48 , C07C251/52 , C07C253/00 , C07C255/50 , C07C317/00 , C07C317/32 , C07C319/00 , C07C319/14 , C07C323/09 , C07D20060101 , C07D261/02 , C07D261/04 , C07D261/08 , C07D413/00 , C07D413/02 , C07D413/10
Abstract: A method for producing isoxazolene of the formula (I), where R1 is hydrogen, C1-C6 alkyl, R2 is C1-C6 alkyl, R3, R4, R5 are hydrogen, C1-C6 alkyl or R4 and R5 together form a bond, R6 is a heterocyclic ring, and n is 0, 1 or 2. Said method comprises the production of an intermediate compound of the formula (VI), where R1, R3, R4 and R5 have the meanings given above. This step is followed by halogenation, thiomethylation, oxidation and acylation to yield compounds of formula (I). The invention also relates to new intermediate products for producing compounds of formula (I).
-
207.
公开(公告)号:EG24781A
公开(公告)日:2010-09-01
申请号:EGNA2006000610
申请日:2006-06-21
Applicant: BASF AG
Inventor: KORDES MARKUS , HOFMANN MICHAEL , PUHL MICHAEL , GOTZ NORBERT , RACK MICHAEL , AUMANN ERNST , DEYN WOLFGANG VON , SCHMIDT THOMAS , TEDESCHI LIVIOEACY , TREACY MICHAEL F , CULBERTSON DEBORAH L , BUCCI TONI , KUHN DAVID G
IPC: A01N43/76 , A01N43/78 , C07D263/28 , C07D277/18
Abstract: The present invention relates to 1-(azolin-2-yl)amino-1,2-diphenylethane compounds of the general formula (I) wherein A is a radical of the formulae A' or A2: NRA'A2 and wherein m is 0, 1, 2, 3, 4 or 5, n is 0, 1, 2, 3, 4 or 5, X is sulfur or oxygen, and wherein the variables R1, R2, R3, R4, R5a, R5b, R5c, R5d are as defined in the claims, and to the agriculturally acceptable salts thereof. The invention relates also to a method of combating animal pests, selected from insects, arachnids and nematodes and to a method for protecting crops from attack or infestation by insects, arachnids or nematodes, which comprises contacting a crop with a pesticidally effective amount of a 1-(azolin-2-yl)amino-1,2-diphenylethane compounds of the general formula I and/or at least one salt thereof.
-
公开(公告)号:EA012526B1
公开(公告)日:2009-10-30
申请号:EA200701839
申请日:2006-03-15
Applicant: BASF AG
Inventor: GRAMMENOS WASSILIOS , RHEINHEIMER JOACHIM , LOHMANN JAN KLAAS , GROTE THOMAS , PUHL MICHAEL , KORADIN CHRISTOPHER , BAUMANN ERNST , VON DEYN WOLFGANG , LANGEWALD JURGEN , GOTZ NORBERT , CULBERTSON DEBORAH L , ANSPAUGH DOUGLAS D , OLOUMI-SADEGHI HASSAN , COTTER HENRY VAN TUYL , KUHN DAVID G
IPC: A01N43/40 , C07D213/42
Abstract: Бифенилсульфонамидыформулы Iвкоторой Rозначаетводород, алкил, аллил, пропаргилилибензил; R, R, R, Rозначаютводород, галоген, алкил, галометил, алкокси, алкилтио, алкиламиноилидиалкиламино; R, Rозначаютводород, гидрокси, циано, нитро, амино, галоген, алкил, галоалкил, алкокси, галоалкокси, алкилтио, С-С-алкилкарбонил, алкоксикарбонил, -C(R)=NOR, алкиламино, диалкиламино, алкиламинокарбонил, диалкиламинокарбонил, необязательнозамещенныйфенилилинеобязательнозамещенныйфенокси; илидва Rилидва Rвместес двумярасположеннымирядомкольцевымичленамифенильногокольца, ккоторомуониприсоеденены, могутобразовыватьнеобязательнозамещенное, аннелированноециклопентильное, циклогексильноеилифенильноекольцо; m принимаетзначенияот 0 до 4; n принимаетзначенияот 0 до 5; сусловием, что m и n неозначаютодновременно 0, есливсе R-Rозначаютводород; Rозначаеталкил; Rозначаеталкил, галоалкил, алкенил, галоалкенил, алкинил, галоалкинилилибензил; Rозначаетциано, нитро, галоген, алкил, галометил, алкоксиилигалометокси; и N-оксидыи сельскохозяйственно-приемлемыесолии ветеринарно-приемлемыесолисоединения I, способполученияэтихсоединений, содержащийихкомпозиции, ихприменениедляборьбыс фитопатогеннымивреднымигрибамии вреднымичленистоногими, способборьбыс членистоногимивредителями, способзащитысельскохозяйственныхкультуротнападенияилизаражениячленистоногимивредителями, способзащитысемяни неживыхматериаловотзаражениячленистоногимивредителями, способзащитынеживыхматериаловотнападенияилизаражениячленистоногимивредителямии семена, содержащиесоединения I.
-
209.
公开(公告)号:EA010872B1
公开(公告)日:2008-12-30
申请号:EA200500598
申请日:2003-10-29
Applicant: BASF AG
Inventor: HAMPRECHT GERHARD , PUHL MICHAEL , REINHARD ROBERT , SEITZ WERNER , WOLF BERND , GOTZ NORBERT , KEIL MICHAEL , SAGASSER INGO
IPC: C07C307/06 , C07C303/34 , C07C331/28 , C07D207/20 , C07D211/18 , C07D211/70 , C07D213/76 , C07D295/26 , C07D307/52 , C07D319/06 , C07D333/20
Abstract: Изобретениеотноситсяк способуполучениябифункциональныхфенилизо(тио)цианатовобщейформулы I сацилсульфамиднойгруппойгдеостаткиимеютследующиезначения: W означаеткислородилисеру, Ar означаетфенил, которыйможетбытьзамещенодинилинесколькоразгалогеном; Аозначает NRR, где Rи Rозначаютнезависимодруготдруга C-C-алкил, C-C-алкенилили C-C-алкинил, либо Rи Rобразуютвместенасыщенный 6-членныйазотныйгетероцикл, которыйможетбытьзамещенС-С-алкилом, взаимодействиеманилиновилиихгидрохлоридовс производнымифосгена. Изобретениеотноситсятакжек бифункциональнымфенилизо(тио)цианатамдляполучениясредствзащитырастений.
-
公开(公告)号:SK286367B6
公开(公告)日:2008-08-05
申请号:SK6792001
申请日:1999-11-06
Applicant: BASF AG
Inventor: MAYWALD VOLKER , STEINMETZ ADRIAN , RACK MICHAEL , GOTZ NORBERT , GOTZ ROLAND , HENKELMANN JOCHEM , BECKER HEIKE , AISCAR BAYETO JUAN JOSE
IPC: C07D231/00 , C07D231/20
Abstract: It is described a method for producing 1-substituted 5- and/or 3-hydroxypyrazoles of formulas (I) and (II), wherein R1 represents C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkinyl, C3-C6-cycloalkyl or C1-C4-alkoxy, whereby these groups can be substituted by halogen, C1-C4-alkoxy, phenoxy, C1-C6-alkoxycarbonyl, C1-C6-alkylthiocarbonyl or a cyclic ring system with 3-14 ring atoms, by reacting a 3-alkoxyacrylic acid alkyl ester of formula (III), wherein R2, R3 independently mean C1-C6-alkyl or C3-C6-cycloalky, with a hydrazine of formula (IV), wherein R1 has the above cited meaning, a) at a pH value of 6-11 to form 5-hydroxypyrazoles of formula (I), or b) at a pH value of 11-14 to form 3-hydroxypyrazoles of formula (II).
-
-
-
-
-
-
-
-
-