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公开(公告)号:WO2006136357A2
公开(公告)日:2006-12-28
申请号:PCT/EP2006005869
申请日:2006-06-19
Applicant: BASF AG , ZIEGLER HANS , MAYER WINFRIED , KROEHL THOMAS , SCHNEIDER KARL-HEINRICH , COX GERHARD , ERK PETER , VOGELBACHER UWE JOSEF , NOACK RAINER , GOETZ ROLAND , WUCKELT JOERG , RAULS MATTHIAS
Inventor: ZIEGLER HANS , MAYER WINFRIED , KROEHL THOMAS , SCHNEIDER KARL-HEINRICH , COX GERHARD , ERK PETER , VOGELBACHER UWE JOSEF , NOACK RAINER , GOETZ ROLAND , WUCKELT JOERG , RAULS MATTHIAS
CPC classification number: A01N47/24 , C07D231/22 , A01N25/04 , A01N25/02 , A01N2300/00
Abstract: The invention relates to novel crystalline modifications to pyraclostrobin, methods for production and use of the novel modifications for the production of plant protection agents.
Abstract translation: 本发明涉及唑菌胺酯的新的结晶变型,它们的制备方法和用于制备作物保护剂使用的新颖的修改的过程。
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公开(公告)号:ME01961B
公开(公告)日:2012-02-29
申请号:MEP47511
申请日:2006-06-19
Applicant: BASF AG
Inventor: GÖTZ ROLAND , WUCKELT JÖRG , RAULS MATTHIAS , ZIEGLER HANS , MAYER WINFRIED , KRÖHL THOMAS , SCHNEIDER KARL-HEINRICH , COX GERHARD , ERK PETER , VOGELBACHER UWE JOSEF , NOACK RAINER
IPC: A01N47/24 , C07D231/22
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公开(公告)号:BRPI0612246A2
公开(公告)日:2011-01-04
申请号:BRPI0612246
申请日:2006-06-19
Applicant: BASF AG
Inventor: ZIEGLER HANS , MAYER WINFRIED , KROEHL THOMAS , SCHNEIDER KARL-HEINRICH , COX GERHARD , ERK PETER , VOGELBACHER UWE JOSEF , NOACK RAINER , GOETZ ROLAND , WUCKELT JOERG , RAULS MATTHIAS
IPC: A01N47/24 , C07D231/22
Abstract: Crystalline modification IV of pyraclostrobin (A) exhibits at least three reflexes in an X-ray powder diffractogram at 25[deg]C, where the reflections (d) are 6.02 +- 0.01 Å, 4.78 +- 0.01 Å, 4.01 +- 0.01 Å, 3.55 +- 0.01 Å and 3.01 +- 0.01 Å. Independent claims are included for: (1) the preparation of (A); (2) crystalline modification II of pyroclostobin (A1) exhibiting at least four reflexes in a X-ray powder diffractogram at 25[deg]C, where the reflections (d) are 5.93 +- 0.01 Å, 5.82 +- 0.01 Å, 4.89 +- 0.01 Å, 4.78 +- 0.01 Å, 4.71 +- 0.01 Å, 3.97 +- 0.01 Å, 3.89 +- 0.01 Å, 3.77 +- 0.01 Å, 3.75 +- 0.01 Å, 3.57 +- 0.01 Å and 3.43 +- 0.01 Å; (3) the preparation of (A1); and (4) a plant protection agent, which comprises pyraclostrobin in the form of modification IV or in the form of modification II and carrier materials and/or additives. ACTIVITY : Fungicide. MECHANISM OF ACTION : None given.
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公开(公告)号:DE102005055841A1
公开(公告)日:2007-05-31
申请号:DE102005055841
申请日:2005-11-23
Applicant: BASF AG
Inventor: HUENGER UDO , NOACK RAINER , GOETZ ROLAND , STUERMER RAINER , LOHMANN JAN KLAAS
IPC: C07D303/36 , B01J31/04 , B01J31/36 , B01J31/38
Abstract: Preparation of an optically active oxirane compound (A) comprises epoxidation of a phenyl compound (A1) using a chiral metal containing epoxidizing catalyst and an oxidizing agent or an achiral metal containing epoxidizing catalyst and a chiral oxidizing agent. Preparation of an optically active oxirane compound (A) of formula (I), (Ib), (Ic) and/or (Id) comprises epoxidation of a phenyl compound (A1) of formula (IIa) or (IIb) using a chiral metal containing epoxidizing catalyst and an oxidizing agent or an achiral metal containing epoxidizing catalyst and a chiral oxidizing agent. R : CH2X, CHO, CH=NR1>, CH=NNR2>, COOH, COOR3>, CONR4>R5> or CN; Rs : CH2OH; X : OH, O-SO2R6> or halo; R1>H, OH, 1-8C alkyl or aryl; R2>H, 1-8C alkyl or aryl; R3>1-8C alkyl, 2-8C hydroxyalkyl or arylalkyl; either R4>, R5>H, 1-8C alkyl, 2-8C hydroxyalkyl, aryl or arylalkyl; or NR4>R5>5-6 membered optionally saturated ring with 1-3 heteroatom; and R6>1-8C (halo)alkyl or aryl. [Image] [Image] ACTIVITY : Fungicide. MECHANISM OF ACTION : None given.
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公开(公告)号:DE50306914D1
公开(公告)日:2007-05-10
申请号:DE50306914
申请日:2003-06-06
Applicant: BASF AG
Inventor: NOACK RAINER , SANDER MICHAEL , HENNINGSEN MICHAEL
IPC: C07D405/06 , C07D521/00
Abstract: The present invention relates to a process for the preparation of 1,2,4-triazol-1-ylmethyloxiranes of the formula I in which A and B are identical or different and, independently of one another, are C 1 -C 4 -alkyl, phenyl-C 1 -C 2 -alkyl, C 3 -C 6 -cycloalkyl, C 3 -C 6 -cycloalkenyl, tetrahydropyranyl, tetrahydrofuranyl, dioxanyl or phenyl, where the phenyl radical can carry one to three substituents chosen from the group: halogen, nitro, C 1 -C 4 -alkyl, C l -C 4 -alkyloxy, phenoxy, amino, C 1 -C 2 -haloalkyl or phenylsulfonyl, which comprises reacting a) an oxirane of the formula II in which A and B have the meanings given above and L is a nucleophilically substitutable leaving group, with 4-amino-1,2,4-triazole of the formula III to give 4-amino-1,2,4-triazolium salts of the formula IV and b) deaminating the 4-amino-1,2,4-triazolium salts IV with alkali metal nitrites and acid or organic nitrites to give 1,2,4-triazol-1-ylmethyloxiranes of the formula I, and to 4-aminotriazolium salts of the formula IV as intermediates.
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公开(公告)号:DK1395579T3
公开(公告)日:2005-04-11
申请号:DK02740595
申请日:2002-05-14
Applicant: BASF AG
Inventor: KAISER REINHARD , SANDER MICHAEL , NOACK RAINER
IPC: C07D405/06
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公开(公告)号:DK1395580T3
公开(公告)日:2005-02-28
申请号:DK02745289
申请日:2002-05-10
Applicant: BASF AG
Inventor: KRAFFZIK REINHOLD , KOARK DIETMAR , NOACK RAINER
IPC: C07D405/06
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公开(公告)号:AT287401T
公开(公告)日:2005-02-15
申请号:AT02740595
申请日:2002-05-14
Applicant: BASF AG
Inventor: SANDER MICHAEL , NOACK RAINER , KAISER REINHARD
IPC: C07D405/06 , C07D521/00
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公开(公告)号:MX2007016271A
公开(公告)日:2008-03-07
申请号:MX2007016271
申请日:2006-06-19
Applicant: BASF AG
Inventor: VOGELBACHER UWE JOSEF , SCHNEIDER KARL-HEINRICH , GOTZ ROLAND , ERK PETER , ZIEGLER HANS , KROHL THOMAS , RAULS MATTHIAS , NOACK RAINER , MAYER WINFRIED , COX GERHARD , WUCKELT JORG
IPC: A01N47/24 , C07D231/22
Abstract: La presente invencion se refiere a las modificaciones cristalinas novedosas de piraclostrobina, a los procedimientos para su preparacion y a la utilizacion de las nuevas modificaciones para preparar agentes fitoprotectores.
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公开(公告)号:BRPI0417433A
公开(公告)日:2007-05-22
申请号:BRPI0417433
申请日:2004-12-14
Applicant: BASF AG
Inventor: NOACK RAINER , RUEB LOTHAR , PALM CLEMENS
IPC: C07C45/74 , C07C47/232 , C07C47/24
Abstract: The invention relates to a method for producing 2,3-cis-substituted 2-aryl propenals by condensing a 2-aryl acetaldehyde I with a non-enolizable aldehyde compound II in the presence of a base. The inventive method is characterized in that the reaction is carried out in a solvent mixture comprising at least one water-miscible organic solvent and water at a volume ratio V solvent :V water ranging between 10:1 and 0.5:1.
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