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    • 102. 发明授权
    • Benzylhydroxylamines and intermediates used to prepare them
    • US6057269A
    • 2000-05-02
    • US973780
    • 1998-01-05
    • Ralf KlintzGerhard HamprechtElisabeth HeistracherPeter SchaferCyrill ZagarKarl-Otto WestphalenHelmut WalterUlf MisslitzOlaf MenkeMarkus Menges
    • Ralf KlintzGerhard HamprechtElisabeth HeistracherPeter SchaferCyrill ZagarKarl-Otto WestphalenHelmut WalterUlf MisslitzOlaf MenkeMarkus Menges
    • A01N43/54A01N47/12A01N47/24A01N47/30A01N53/00C07C239/08C07C239/10C07C239/16C07C239/20C07C265/12C07C271/22C07C271/28C07C271/54C07C271/58C07C275/32C07C275/40C07D239/54C07D405/12
    • C07D239/54A01N43/54A01N47/12A01N47/24A01N47/30A01N53/00C07C239/08C07C239/10C07C265/12C07C271/22C07C271/28C07C271/54C07C271/58C07C275/40
    • Benzylhydroxylamines I ##STR1## (X=--N(R.sup.7)--O--; Y=O, S; R.sup.1 =halogen, CN, NO.sub.2, CF.sub.3 ; R.sup.2 =H, halogen; R.sup.3 =H, NH.sub.2, CH.sub.3 ;R.sup.4 =H, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylsulfinyl or C.sub.1 -C.sub.6 -alkylsulfonyl;R.sup.5 =H, halogen, C.sub.1 -C.sub.6 -alkyl;R.sup.6 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.2 -C.sub.6 -alkenyl;R.sup.7 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.3 -C.sub.6 -alkenylcarbonyl, C.sub.3 -C.sub.6 -alkynylcarbonyl, C.sub.1 -C.sub.6 -alkoxycarbonyl, C.sub.2 -C.sub.8 -alkenyloxycarbonyl, C.sub.2 -C.sub.6 -alkynyloxycarbonyl, C.sub.1 -C.sub.6 -alkylthiocarbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylcarbamoyl, it being possible for the 14 last-mentioned radicals to have attached to them 1-3 substituents:NO.sub.2, CN, halogen, C.sub.3 -C.sub.8 -cycloalkyl, OH, C.sub.1 -C.sub.6 -alkoxy, C.sub.3 -C.sub.8 -cycloalkoxy, C.sub.3 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyloxy, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylcarbonyl, C.sub.1 -C.sub.6 -alkylcarbonyloxy, C.sub.1 -C.sub.6 -alkylsulfinyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylideneaminoxy, C.sub.1 -C.sub.6 -alkylcarbamoyl,unsubstituted or substituted phenyl, phenoxy or phenylsulfonyl,a 3- to 7-membered heterocyclyl or heterocyclyloxy group having 1-3 hetero atoms, it being possible for this group to be saturated, unsaturated or aromatic and to have attached to it 1-3 substituents,--CO--Z.sup.1 R.sup.9, --OCO--Z.sup.1 R.sup.9, --N(R.sup.9)R.sup.10 orR.sup.7 =unsubstituted or substituted cycloalkylcarbonyl, phenylcarbonyl, phenylsulfonyl, phenylcarbamoyl;R.sup.8 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -alkenyl or C.sub.3 -C.sub.6 -alkynyl, it being possible for each of the 5 last-mentioned radicals to have attached to it 1-3 substituents:NO.sub.2, CN, halogen, C.sub.3 -C.sub.8 -cycloalkyl, OH, C.sub.1 -C.sub.6 -alkoxy, C.sub.3 -C.sub.8 -cycloalkoxy, C.sub.3 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyloxy, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylthio, C.sub.1 -C.sub.6 -alkylsulfinyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.1 -C.sub.6 -alkylideneaminoxy,unsubstituted or substituted phenyl- [sic], phenoxy-[sic] or phenylsulfonyl,a 3- to 7-membered heterocyclyl or heterocyclyloxy group having 1-3 hetero atoms, it being possible for this group to be saturated, unsaturated or aromatic and to have attached to it 1-3 substituents,--CO--Z.sup.2 R.sup.11, --OCO--Z.sup.2 R.sup.11, --N(R.sup.11)R.sup.12 ;Z.sup.1 a chemical bond, oxygen, sulfur or --N(R.sup.10)--;Z.sup.2 =a chemical bond, oxygen, sulfur or --N(R.sup.12)--;R.sup.9, R.sup.11 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkyl, (C.sub.1 -C.sub.6 -alkoxy)carbonyl-C.sub.1 -C.sub.6 -alkyl, unsubstituted or substituted phenyl or phenyl-C.sub.1 -C.sub.6 -alkyl,orZ.sup.1 and R.sup.9 and/or Z.sup.2 and R.sup.11 together=a 3- to 7-membered heterocycle having 1-3 hetero atoms and bonded via nitrogen, it being possible for this heterocycle to be saturated, unsaturated or aromatic and, if desired, to have attached to it one to three substituents,R.sup.10, R.sup.12 =H, OH, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl, C.sub.1 -C.sub.6 -alkoxy)and the salts of I where R.sup.3, R.sup.7 and/or R.sup.8 =hydrogenare used as herbicides and for the desiccation/defoliation of plants.
    • 103. 发明授权
    • Substituted triazolinones as crop protection agents
    • 取代三唑啉酮作为作物保护剂
    • US5885934A
    • 1999-03-23
    • US793152
    • 1997-02-18
    • Elisabeth HeistracherChristoph Sweder von dem Bussche-HunnefeldGerhard HamprechtRalf KlintzPeter SchaferKarl-Otto WestphalenMatthias GerberHelmut Walter
    • Elisabeth HeistracherChristoph Sweder von dem Bussche-HunnefeldGerhard HamprechtRalf KlintzPeter SchaferKarl-Otto WestphalenMatthias GerberHelmut Walter
    • A01N43/653C07D249/12
    • A01N43/653C07D249/12
    • Substituted triazolinones I ##STR1## where R.sup.1 and R.sup.2 are each H, C.sub.1 -C.sub.6 -alkyl or C.sub.1 -C.sub.6 -haloalkyl,R.sup.3 is H or halogen,R.sup.4 is CN, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -alkoxy or C.sub.1 -C.sub.6 -haloalkoxy,R.sup.5 is NO.sub.2, CN or halogen,R.sup.6 is --OR.sup.7, --SR.sup.7, --N(R.sup.8)--R.sup.9 or --N(R.sup.8)--OR.sup.10,R.sup.7 is H, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.1 -C.sub.6 -haloalkyl, cyano-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkylthio-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxycarbonyl-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkylaminocarbonyl-C.sub.1 -C.sub.6 -alkyl, di-(C.sub.1 -C.sub.6 -alkyl)aminocarbonyl-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoximino-C.sub.1 -C.sub.6 -alkyl, di-(C.sub.1 -C.sub.6 -alkoxy)-C.sub.2 -C.sub.6 -alkyl, di-(C.sub.1 -C.sub.6 -alkylthio)-C.sub.2 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -haloalkenyl or unsubstituted or substituted phenyl or benzyl,R.sup.8, R.sup.9 and R.sup.10 are each C.sub.1 -C.sub.6 -alkylcarbonyl or C.sub.1 -C.sub.6 -haloalkyl-carbonyl or each have one of the meanings stated for R.sup.7,R.sup.8 and R.sup.9 together form a 4- to 6-membered carbon chain in which one methylene unit may be replaced by oxygen or C.sub.1 -C.sub.4 -alkylimino, and the salts of I are used as herbicides or for the desiccation/defoliation of plants.
    • PCT No.PCT / EP95 / 02167 Sec。 371日期1997年2月18日 102(e)日期1997年2月18日PCT Filed June 7,1995 PCT Pub。 公开号WO96 / 05179 日期1996年2月22日三取代三唑啉酮I其中R 1和R 2各自为H,C 1 -C 6烷基或C 1 -C 6卤代烷基,R 3为H或卤素,R 4为CN,卤素,C 1 -C 6烷基, C1-C6-卤代烷基,C1-C6-烷氧基或C1-C6-卤代烷氧基,R5是NO2,CN或卤素,R6是-OR7,-SR7,-N(R8)-R9或-N(R8)-OR10, R7是H,C1-C6-烷基,C3-C6-烯基,C3-C6-炔基,C3-C6-环烷基,C1-C6-卤代烷基,氰基-C1-C6-烷基,C1-C6-烷氧基C1- C 1 -C 6烷基,C 1 -C 6烷基硫基-C 1 -C 6烷基,C 1 -C 6烷氧基羰基-C 1 -C 6烷基,C 1 -C 6烷基氨基羰基-C 1 -C 6烷基,二(C 1 -C 6烷基)氨基羰基 -C 1 -C 6 - 烷基,C 1 -C 6 - 烷氧基-C 1 -C 6 - 烷基,二 - (C 1 -C 6 - 烷氧基)-C 2 -C 6烷基,二 - (C 1 -C 6 - 烷硫基)-C 2 -C 6烷基 ,C 3 -C 6 - 卤代链烯基或未取代或取代的苯基或苄基,R 8,R 9和R 10各自为C 1 -C 6 - 烷基羰基或C 1 -C 6卤代烷基 - 羰基,或者各自具有R7,R8和R9所述的含义 其中一个亚甲基单元可被氧或C 1 -C 4烷基亚氨基取代的4-至6-元碳链,其中I ar e用作除草剂或用于植物的干燥/脱叶。
    • 104. 发明授权
    • Substituted 1-amino-3-phenyluracils
    • 取代的1-氨基-3-苯基尿嘧啶
    • US5700805A
    • 1997-12-23
    • US596215
    • 1996-02-15
    • Peter SchaferRalf KlintzGerhard HamprechtElisabeth HeistracherKarl-Otto WestphalenMatthias GerberHelmut Walter
    • Peter SchaferRalf KlintzGerhard HamprechtElisabeth HeistracherKarl-Otto WestphalenMatthias GerberHelmut Walter
    • A01N43/54C07D239/54C07D239/56C07D405/10C07D409/10C07D411/10
    • C07D239/54A01N43/54C07D405/10C07D409/10C07D411/10
    • Substituted 1-amino-3-phenyluracils I ##STR1## where the variables have the following meanings: R.sup.1 =H, F, Cl; Y=O, S; Z=--CH=N--OH, --CH=N--O--(alkyl), --CH=N--O--(alkylene)--O--(alkyl), --CH=N--O--CH.sub.2 --COOH, --CH=N--O--CH(alkyl)--COOH, --CH=N--O--CH.sub.2 --CO--O--(alkyl), --CH=N--O--CH(alkyl)--CO--O--(alkyl), --CH=N--O--CH.sub.2 --CO--O=O-- (alkylene)--O--(alkyl), --CH=N--O--CH(alkyl)--CO--O-- (alkylene)--O--(alkyl), --CH=CH--CO--O--(alkyl), --CH=CH-- CO--O--(alkylene)--O--(alkyl), --CH=C(Cl)--CO--O--(alkyl), --CH=C(Br)--CO--O--(alkyl), --CH=C(Cl)--CO--O--(alkylene)--O--(alkyl), --CH=C(Br)--CO--O--(alkylene)--O--(alkyl), --CH=C(CH.sub.3)--CO--O--(alkyl), --CH=C(CH.sub.3)--CO--O--(alkylene)--O--(alkyl), --CH�X.sup.1 -(alkyl)! �X.sup.2 -(alkyl)! or a radical ##STR2## X.sup.1 -X.sup.6 =O, S; R.sup.2 -R.sup.11 =H, alkyl, vinyl, alkoxycarbonyl are described. Use: herbicides; desiccation/defoliation of plants.
    • PCT No.PCT / EP94 / 02821 Sec。 371日期:1996年2月15日 102(e)日期1996年2月15日PCT 1994年8月25日PCT公布。 公开号WO95 / 06641 日期1995年3月9日取代的1-氨基-3-苯基尿嘧啶I,其中变量具有以下含义:R1 = H,F,Cl; Y = O,S; Z = -CH = N-OH,-CH = NO-(烷基),-CH = NO-(亚烷基)-O-(烷基),-CH = NO-CH 2 -COOH,-CH = )-COOH,-CH = NO-CH 2 -CO-O-(烷基),-CH = NO-CH(烷基)-CO-O-(烷基),-CH = NO-CH 2 -CO-O = O- (亚烷基)-O-(烷基),-CH = NO-CH(烷基)-CO-O-(亚烷基)-O-(烷基),-CH = CH-CO-O-(烷基) CH-CO-O-(亚烷基)-O-(烷基),-CH = C(C1)-CO-O-(烷基),-CH = C(Br)-CO-O- = C(Cl)-CO-O-(亚烷基)-O-(烷基),-CH = C(Br)-CO-O-(亚烷基)-O-(烷基),-CH = C(CH 3) CO-O-(烷基),-CH = C(CH3)-CO-O-(亚烷基)-O-(烷基),-CH [X1-(烷基)] [X2-(烷基) 图像> X1-X6 = O,S; 描述了R2-R11 = H,烷基,乙烯基,烷氧基羰基。 用途:除草剂; 植物的干燥/脱叶。
    • 109. 发明授权
    • Substituted 3-phenylisoxazolines
    • US6150303A
    • 2000-11-21
    • US463246
    • 2000-01-21
    • Olaf MenkeMarkus MengesGerhard HamprechtRobert ReinhardPeter SchaferCyrill ZagarKarl-Otto WestphalenUlf MisslitzHelmut Walter
    • Olaf MenkeMarkus MengesGerhard HamprechtRobert ReinhardPeter SchaferCyrill ZagarKarl-Otto WestphalenUlf MisslitzHelmut Walter
    • A01N43/80C07D261/04A01N43/72
    • C07D261/04
    • Substituted 3-phenylisoxazolines I, and their salts and enol ethers, are described as herbicides ##STR1## where X.dbd.--O--, --S--, --N(R.sup.9)--;R.sup.1 .dbd.CN, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -haloalkoxy, C.sub.1 -C.sub.4 -alkylsulfonyl;R.sup.2 .dbd.H or unsubstituted or substituted C.sub.1 -C.sub.6 -alkyl, (C.sub.1 -C.sub.6 -alkyl)carbonyl, C.sub.1 -C.sub.6 -alkylsulfonyl, C.sub.2 -C.sub.6 -alkenyl, (C.sub.2 -C.sub.6 -alkenyl)carbonyl, C.sub.2 -C.sub.6 -alkynyl, (C.sub.2 -C.sub.6 -alkynyl)carbonyl;R.sup.3 .dbd.H, halogen;R.sup.4 .dbd.CN, halogen, C.sub.1 -C.sub.3 -haloalkyl;R.sup.5 .dbd.H, CN, halogen, C.sub.1 -C.sub.3 -haloalkyl;R.sup.6 .dbd.H, CN, halogen, C.sub.1 -C.sub.3 -haloalkyl or unsubstituted or substituted C.sub.1 -C.sub.6 -alkoxy;R.sup.7 .dbd.CN, halogen;R.sup.8 in position .alpha., R.sup.7 in this case being in position .beta., or in position .beta., R.sup.7 in this case being in position .alpha., is1) H, OH, SH, CN, NO.sub.2, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.1 -C.sub.6 -haloalkoxy, C.sub.1 -C.sub.6 -haloalkylthio, C.sub.1 -C.sub.6 -alkylthio-(C.sub.1 -C.sub.6 -alkyl)carbonyl, (C.sub.1 -C.sub.6 -alkyl)iminooxycarbonyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxyamino-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkylamino-C.sub.1 -C.sub.6 -alkyl,2) unsubstituted or substituted C.sub.1 -C.sub.6 -alkoxy, C.sub.1 -C.sub.6 -alkylthio, C.sub.3 -C.sub.6 -cycloalkoxy, C.sub.3 -C.sub.6 -cycloalkylthio, C.sub.2 -C.sub.6 -alkenyloxy, C.sub.2 -C.sub.6 -alkenylthio, C.sub.2 -C.sub.6 -alkynyloxy, C.sub.2 -C.sub.6 -alkynylthio, (C.sub.1 -C.sub.6 -alkyl)carbonyloxy, (C.sub.1 -C.sub.6 -alkyl)carbonylthio, (C.sub.1 -C.sub.6 -alkoxy)carboxyloxy, (C.sub.2 -C.sub.6 -alkenyl)carbonyloxy, (C.sub.2 -C.sub.6 -alkenyl)carbonylthio, (C.sub.2 -C.sub.6 -alkynyl)carbonyloxy, (C.sub.2 -C.sub.6 -alkynyl)carbonylthio, C.sub.1 -C.sub.6 -alkylsulfonyloxy or C.sub.1 -C.sub.6 -alkylsulfonyl,3) 29 further radicals;R.sup.9 .dbd.H, C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkyl, (C.sub.1 -C.sub.6 -alkoxy)carbonyl-C.sub.1 -C.sub.6 -alkyl, (C.sub.3 -C.sub.6 -alkenyloxy)carbonyl-C.sub.1 -C.sub.6 -alkyl, unsubstituted or substituted phenyl or phenyl-C.sub.1 -C.sub.6 -alkyl.
    • 110. 发明授权
    • Substituted cinnamic oxime and hydroxamide derivatives
    • 取代的肉桂肟和羟基酰胺衍生物
    • US6013606A
    • 2000-01-11
    • US765180
    • 1997-06-30
    • Ralf KlintzGerhard HamprechtElisabeth HeistracherPeter SchaferChristoph-Sweder von dem Bussche-HunnefeldPeter MunsterReinhard KirstgenAlbrecht HarreusKarl-Otto WestphalenMatthias GerberHelmut Walter
    • Ralf KlintzGerhard HamprechtElisabeth HeistracherPeter SchaferChristoph-Sweder von dem Bussche-HunnefeldPeter MunsterReinhard KirstgenAlbrecht HarreusKarl-Otto WestphalenMatthias GerberHelmut Walter
    • C07D239/52A01N37/32A01N37/50A01N43/38A01N43/54C07C251/40C07C259/06C07C265/14C07C271/28C07C271/58C07C331/28C07D209/48C07D239/54C07D239/56C07D239/58C07D413/10A01N43/50C07D223/10C07D235/26
    • C07D209/48A01N37/32A01N37/50A01N43/54C07C251/40C07C259/06C07C265/14C07C271/28C07C271/58C07C331/28C07D239/54
    • Substituted cinnamic oxime derivatives I and cinnamic hydroxamide derivatives II ##STR1## (R.sup.1= halogen, NO.sub.2, CN, CF.sub.3 ; R.sup.2 =H, halogen; R.sup.3= H, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, hydroxy-C.sub.1 -C.sub.6 -alkyl;R.sup.4= H, halogen, CN, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl orR.sup.3 +R.sup.4 =chemical bond;Y=--O--, --S--, --O--CO--, --O--SO.sub.2 -- or chemical bond;Y'=--O-- or --S--;R.sup.5= unsubst. or subst. C.sub.1 -C.sub.6 -alkyl or C.sub.1 -C.sub.6 -haloalkyl; C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, unsubst. or subst. phenyl or phenyl-C.sub.1 -C.sub.6 -alkyl, or, if Y is --O--, --S-- or a chemical bond, is (C.sub.1 -C.sub.6 -alkyl)carbonyl or (C.sub.1 -C.sub.6 -alkoxy)carbonyl; or, if Y is a chemical bond, is hydrogen or halogen;R.sup.5 '=R.sup.5, H or (C.sub.1 -C.sub.6 -haloalkyl)carbonyl;R.sup.6= H, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl, hydroxy-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxy-C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkylthio-C.sub.1 -C.sub.6 -alkyl, cyano-C.sub.1 -C.sub.6 -alkyl, (C.sub.1 -C.sub.6 -alkoxy) carbonyl-C.sub.1 -C.sub.6 -alkyl, (C.sub.1 -C.sub.6 -alkyl) carbonyl-C.sub.1 -C.sub.6 -alkyl, (C.sub.1 -C.sub.6 -alkyl)carbonyloxy-C.sub.1 -C.sub.6 -alkyl or unsubst. or subst. phenyl-C.sub.1 -C.sub.6 -alkyl;or, if Y is oxygen or sulfur, R.sup.5 +R.sup.6 together=unsubst. or subst. C.sub.1 -C.sub.3 -alkylene;Cyc=N-(3,4,5,6-tetrahydrophthalimido) or ##STR2## X.sup.1, X.sup.2 =oxygen or sulfur; R.sup.7 =H, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, NH.sub.2 ;R.sup.8, R.sup.9 =H, halogen, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl or unsubst. or subst. phenyl);and salts of I and II.Use: herbicides; desiccation/defoliation of plants.
    • PCT No.PCT / EP95 / 02584第 371日期:1997年6月30日 102(e)日期1997年6月30日PCT提交1995年7月4日PCT公布。 第WO96 / 02518号公报 日期1996年2月1日取代肉桂肟衍生物I和肉桂酸羟基酰胺衍生物II(R1 =卤素,NO2,CN,CF3; R2 = H,卤素; R3 = H,卤素,C1-C6-烷基,C1-C6-卤代烷基, C3-C6-环烷基,C3-C6-烯基,C3-C6-炔基,羟基-C1-C6-烷基; R4 = H,卤素,CN,C1-C6-烷基,C1-C6-卤代烷基或R3 + R4 = 化学键; Y = -O-,-S-,-O-CO-,-O-SO2-或化学键; Y'= -O-或-S-; R5 =未取代或未取代的C1-C6- 烷基或C 1 -C 6 - 卤代烷基; C 3 -C 6 - 环烷基,C 3 -C 6 - 烯基,C 3 -C 6炔基,未取代或取代的苯基或苯基-C 1 -C 6烷基,或者如果Y是-O- (C 1 -C 6烷基)羰基或(C 1 -C 6 - 烷氧基)羰基;或者如果Y是化学键,则是氢或卤素; R 5'= R 5,H或(C 1 -C 6 - -C 6 - 卤代烷基)羰基; R 6 = H,C 1 -C 6烷基,C 1 -C 6卤代烷基,C 3 -C 6环烷基,C 3 -C 6 - 烯基,C 3 -C 6炔基,羟基-C 1 -C 6烷基, C 1 -C 6烷氧基-C 1 -C 6烷基,C 1 -C 6烷硫基-C 1 -C 6烷基,氰基-C 1 -C 6烷基,(C 1 -C 6 - 烷氧基)羰基-C 1 -C 6烷基,(C 1 -C 6 - 烷基)羰基-C 1 -C 6 - 烷基,(C 1 -C 6 - 烷基)羰基氧基 -C 1 -C 6 - 烷基或未取代基。 或subst。 苯基-C 1 -C 6 - 烷基; 或者如果Y是氧或硫,则R5 + R6一起=不成立。 或subst。 C1-C3-亚烷基; Cyc = N-(3,4,5,6-四氢邻苯二甲酰亚氨基)或X1,X2 =氧或硫; R7 = H,C1-C6-烷基,C1-C6-卤代烷基,NH2; R8,R9 = H,卤素,C1-C6-烷基,C1-C6-卤代烷基或未取代基。 或subst。 苯基); 和I和II的盐。 用途:除草剂; 植物的干燥/脱叶。