会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 3. 发明申请
    • SUBSTITUTED OXAZACYCLOALKENES, INTERMEDIATE PRODUCTS AND USE AS FUNGICIDES
    • 取代OXAZACYCLOALKENE,中间体和使用作为杀真菌剂
    • WO1995021833A1
    • 1995-08-17
    • PCT/EP1995000311
    • 1995-01-30
    • BAYER AKTIENGESELLSCHAFTSEITZ, ThomasASSMANN, LutzGAYER, HerbertGERDES, PeterHEINEMANN, UlrichKRÜGER, Bernd-WielandKUHNT, DietmarTIEMANN, RalfDEHNE, Heinz-WilhelmDUTZMANN, StefanHÄNSSLER, GerdSTENZEL, Klaus
    • BAYER AKTIENGESELLSCHAFT
    • C07D265/08
    • C07D265/08A01N43/72A01N43/76A01N43/78C07C251/48C07D263/14C07D267/06
    • Substituted oxazacycloalkenes of formula (I) in which A is optionally substituted alkane diyl (alkylene), Ar is optionally substituted arylene or heteroarylene; E is a 1-alkene-1,1-diyl group containing a radical R in the 2nd position or a 2-aza-1-alkene-1,1-diyl group containing a radical R in the 2nd position, or a 3-aza-1-propene-2,3-diyl group containing a radical R in the 3rd position and a radical R in the 1st position, or a 1-aza-1-propene-2,3-diyl group containing a radical R in the 1st position, or a 1,3-diaza-1-propene-2,3-diyl group containing a radical R in the 3rd position and a radical R in the 1st position, or an optionally substituted imino group ("azamethylene", N-R ), G is oxygen or, optionally substituted by halogen, hydroxy, alkyl, halogen alkyl or cycloalkyl, alkane diyl or one of the groups: -Q-CQ-, -CQ-Q-, -CH2-Q-, -Q-CH2-, -CQ-Q-CH2-, -CH2-Q-CQ-, -Q-CQ-CH2-, -Q-CQ-Q-CH2-, -N=N-, -S(O)n-, -CH2-S(O)n-, -CQ-, -S(O)n-CH2-, -C(R )=N-O-, -C(R )=N-O-CH2-, -N(R )-, -CQ-N(R )-, -N(R )-CQ-, -Q-CQ-N(R )-, -N=C(R )-Q-CH2-, -CH2-O-N=C(R )-, -N(R )-CQ-Q-, -CQ-N(R )-CQ-Q-, -N(R )-CQ-Q-CH2-, -CQ-CH2- oder -N=N-C(R )=N-O-; Z is optionally substituted alkyl, alkenyl, alkinyl, cycloalkyl, aryl or heterocyclyl, a process for their production and the use of oxazacycloalkenes as fungicides.
    • 取代的式(I),其中A代表任选取代的烷二基(亚烷基),Ar是任选取代的亚芳基或亚杂芳基的Oxazacycloalkene,E表示的1-烯烃-1,1-二基分组这在2- 定位一个基团R <1>包含,或者是2-氮杂-1-链烯-1,1-二基分组其中基团R <2>包含2位或3-氮杂 其中基团R和1位在位置3包含一个基团R <1>,或代表1-氮杂-1-丙烯-2,3-二基部分的丙烯-2,3-二基分组 是一个基团R <2>包含在1-位,或表示1,3-二氮杂-1-丙烯-2,3-二基,其分组在3位的基团R和在1-位 一个基团R <2>包含,或(“azamethylene”,NR <3>)是任选取代的亚氨基,G表示氧,在每种情况下任选地被卤素,羟基,烷基,卤代烷基或环烷基取代的烷二基,或其中一个取代的 下面-Q-CQ-分组是,-CQ-Q-,-CH 2 -Q-,-Q-CH 2 - ,-CQ-Q-CH2-,-CH2-Q-CQ-,-Q-CQ-CH2- ,-Q-CQ-Q-CH 2 - , - N = N-,-S(O)N-,-CH 2 S(O)N-,-CQ-,-S(O)N-CH 2 - , - C(R <4>)= NO-,-C(R <4>)= NO-CH 2 - ,-N(R <5>) - ,-CQ-N(R <5>) - , - N( [R <5>) - CQ-,-Q-CQ-N(R <5>) - , - N = C(R <4>) - Q-CH2-,-CH2-ON = C(R <4> ) - , - N(R <5>) - CQ-Q-,-CQ-N(R <5>) - CQ-Q,-N(R <5>) - CQ-Q-CH2 - CQ-CH 2或-N = NC(R <4>)= NO-,Z代表任选取代的烷基,烯基,炔基,环烷基,芳基或杂环基,一种方法和用于制备它们的中间体和使用作为Oxazacycloalkenen 杀菌剂。
    • 5. 发明申请
    • HYDROXAMIC-ACID DERIVATIVES, METHOD OF PREPARING THEM AND THEIR USE AS FUNGICIDES
    • 异羟肟酸衍生物,生产和使用作为杀真菌剂方法
    • WO1995020570A1
    • 1995-08-03
    • PCT/EP1995000149
    • 1995-01-16
    • BAYER AKTIENGESELLSCHAFTKRÜGER, Bernd-WielandASSMANN, LutzGAYER, HerbertGERDES, PeterHEINEMANN, UlrichKUHNT, DietmarSEITZ, ThomasGALLENKAMP, BerndTIEMANN, RalfHÄNSSLER, GerdDEHNE, Heinz-WilhelmDUTZMANN, Stefan
    • BAYER AKTIENGESELLSCHAFT
    • C07C259/06
    • C07D213/53A01N37/50A01N43/16C07C259/06C07D239/52C07D285/08C07D333/32C07D417/04
    • The invention concerns hydroxamic-acid derivatives of general formula (I) in which A is hydrogen or a grouping which can be easily splitt off, A is hydrogen or alkyl, Ar is an optionally substituted arylene or hetero-arylene group, E is a 1-alkene-1,1-diyl grouping containing an R group in the 2-position or is a 2-aza-1-alkene-1,1-diyl grouping containing an R group in the 2-position or is an optionally substituted imino (azamethylene, N-R ) grouping, G is oxygen or alkanediyl, alkenediyl or alkynediyl (in each case optionally substituted by halogen, hydroxy, alkyl, haloalkyl or cycloalkyl) or one of the following groupings: -Q-CQ-, -CQ-Q-, -CH2-Q-, -Q-CH2-, -CQ-Q-CH2-, -CH2-Q-CQ-, -Q-CQ-CH2-, -Q-CQ-Q-CH2-, -N=N-, -S(O)n-, -CH2-S(O)n-, -CQ-, -S(O)n-CH2-, -C(R )=N-O-, -C(R )=N-O-CH2-, -N(R )-, -CQ-N(R )-, -N(R )-CQ-, -Q-CQ-N(R )-, -N=C(R )-Q-CH2-, -CH2-O=N-C(R )-, -N(R )-CQ-Q-, -CQ-N(R )-CQ-Q- or -N(R )-CQ-Q-CH2- or optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, aryl or heterocyclyl. The invention also concerns a method of preparing such compounds and their use as fungicides. .
    • 通式(I),其中A代表氢或一个容易裂解的基团,A的异羟肟酸衍生物<1>是氢或烷基,Ar表示在每种情况下任选被取代的亚芳基或亚杂芳基,E表示的1-烯烃 - 1, 它包含在2位置R <1>的基团,或1二基分组表示2-氮杂-1-烯-1,1-二基分组其中2位是一个基团R <2 >包含,或任选取代的亚氨基分组(“azamethylene”,NR <3>)中,G表示氧,代表各自任选被卤素,羟基,烷基,卤代烷基或环烷基取代的烷二基,烯二,alkinediyl或以下中的一个取代的 分组-Q-CQ-,-CQ-Q-,-CH 2 -Q-,-Q-CH 2 - ,-CQ-Q-CH2-,-CH2-Q-CQ-,-Q-CQ-CH 2 - , - Q-CQ-Q-CH 2 - , - N = N-,-S(O)N-,-CH 2 S(O)N-,-CQ-,-S(O)N-CH 2 - ,-C( [R <4>)= NO-,-C(R <4>)= NO-CH 2 - ,-N(R <5>) - ,-CQ-N(R <5>) - , - N(R < 5>) - CQ-,-Q-CQ-N(R <5>) - , - N = C(R <4>) - Q-CH2-,-CH2-O = NC(R <4>) - ,-N(R <5> )-CQ-Q-,-CQ-N(R <5>) - CQ-Q-,或-N(R <5>) - CQ-Q-CH 2 - ,分别表示任选取代的烷基,烯基,炔基, 环烷基,芳基或杂环基,它们的制备和它们作为杀真菌剂的用途。
    • 7. 发明申请
    • SUBSTITUTED 1,2,3,4-TETRAHYDRO-5-NITRO PYRIMIDINES
    • 取代1,2,3,4-四HYDRO -5-硝基 - 嘧啶
    • WO1995019977A1
    • 1995-07-27
    • PCT/EP1995000058
    • 1995-01-09
    • BAYER AKTIENGESELLSCHAFTKRÜGER, Bernd-WielandUHR, HermannKANELLAKOPULOS, JohannesGESING, Ernst, RudolfWOLF, HilmarTURBERG, AndreasMENCKE, NorbertERDELEN, ChristophWACHENDORFF-NEUMANN, UlrikeHARTWIG, Jürgen
    • BAYER AKTIENGESELLSCHAFT
    • C07D401/12
    • C07D401/12A01N43/54A01N43/90A01N47/12C07D487/04
    • The present invention relates to novel substituted 1,2,3,4-tetrahydro-5-nitro pyridines of formula (I) in which Het is possibly substituted pyridyl or thiazolyl, R is C1-4 alkyl, R is C1-4 alkyl, R and R together with the bordering atoms form a saturated 5 or 6 ring possibly containing N or O as a further hetero-atom and is possibly substituted, A is straight-chained or branched alkylene with at least 2 C atoms, possibly substituted by phenyl, halogen, OH, CN or the radical NR R , in which R or R is hydrogen, C1-4 alkyl or phenyl, and possibly interrupted singly or multiply by O, S, (a) or (b), and further, A is possibly substituted cycloalkylene, R represents the radicals (c) or (d) or (e), in which R is alkyl, cycloalkyl, alkenyl, aryl, aralkyl, heteroaryl, alkoxy, cycloalkoxy, alkenoxy, aryloxy, aralkoxy, heteroaryloxy, alkylthio, arylthio, aralkylthio, heteroarylthio, amino, alkylamino, dialkylamino, arylamino, arylalkylamino, aralkylamino, aralkylalkylamino, in which the radicals may be substituted, X is oxygen or sulphur, R is hydrogen or C1-4 alkyl. Processes for their production and their use as parasiticides and ectoparasiticides.
    • 本发明涉及新的取代的式(I)的其中Het代表任选取代的吡啶基或噻唑基,R <1> 1,2,3,4-四氢-5-硝基 - 嘧啶是C 1-4烷基, [R <2>代表C 1-4烷基,R <1>和R <2>连同相邻原子形成饱和的5-或6-元环,任选地含有作为另外的杂原子N或O,且任选地被取代的, 的直链或支链亚具有至少2个碳原子,其任选地被苯基,卤素,OH,CN或基团NR <4> - [R <5>,其中R <4>或R <5>是氢,C 1取代的 -4烷基或苯基,取代的,和任选地单取代或多取代由O,S,(a)或(b)中被中断,此外,A是任选取代的亚环烷基,R <3>代表的基团(C )或(d)或(e)其中R <6>是烷基,环烷基,烯基,芳基,芳烷基,杂芳基,烷氧基,环烷氧基,链烯氧基,芳氧基,芳烷氧基,杂 芳氧基,烷硫基,芳硫基,芳烷硫基,杂芳硫基,氨基,烷基氨基,二烷基氨基,芳基氨基,芳基 - 烷基氨基,芳烷基氨基,芳烷基 - 烷基氨基,其中可以为基团被任选地取代,X表示氧或硫,R <7>是氢 或C 1-4烷基。 其制备方法以及它们作为杀虫剂和杀体外寄生虫使用。
    • 8. 发明申请
    • PYRIDYL-THIAZOLES AND THEIR USE TO PROTECT PLANTS AGAINST INFECTIONS BY MICRO-ORGANISMS
    • 吡啶基噻唑和它们用于植物抵抗感染的微生物保护
    • WO1996037493A1
    • 1996-11-28
    • PCT/EP1996002052
    • 1996-05-14
    • BAYER AKTIENGESELLSCHAFTGALLENKAMP, BerndSTENZEL, KlausHÄNSSLER, GerdDUTZMANN, StefanDEHNE, Heinz-Wilhelm
    • BAYER AKTIENGESELLSCHAFT
    • C07D417/04
    • C07D417/04A01N43/78A01N47/36C07D213/61C07D417/14
    • New pyridyl-thiazoles have the formula (I), in which R stands for alkyl or for the groups (a) or (b), in which R stands for hydrogen or -CO-R , R stands for hydrogen or -CO-R , R stands for hydrogen or alkyl, R stands for alkoxy or dialkylamino, R and R represent independently from each other alkyl, alkoxycarbonyl, alkylamino, optionally substituted aryl, optionally substituted arylamino or optionally substituted arylsulfonylamino, or R and R form together with the nitrogen atom to which they are bound a cyclic imide having the formula (c), in which A stands for optionally substituted alkandiyl or optionally substituted alkendiyl; X stands for hydrogen or halogen and X for halogen. Also disclosed are the salts and acid addition products of these new substances, a process for preparing them and their use for protecting plants against infections by undesirable micro-organisms, as well as new intermediate products having the formulas (IIa), (X) and (XI), in which X , X , X , R and R have the meanings given in the description. The compounds having the formula (XI), as well as their salts and acid addition products, are suitable for protecting plants against infections by undesirable micro-organisms.
    • 式(I),其中R是烷基,新的吡啶基噻唑(a)或(b)中,其中R <1> <5>表示氢或-CO-R R <2>是氢或 - CO-R <6>,R <3>是氢或烷基,R <4>表示烷氧基或二烷基氨基,R <5>和R <6>独立地是烷基,烷氧基羰基,烷基氨基,任选取代的芳基, 任选取代的芳基氨基或任选取代的芳基磺酰氨基,或R <1>和R <2>与它们所连接的氮原子,(c)该式中,a表示任选被取代的烷二基或任选的环状酰亚胺一起 链烯二基,X <1>是氢或卤素,和X <2>表示卤素,和它们的盐和酸加成盐,用于制备新的物质及其对有害微生物保护植物免受攻击的用途。 式新的中间体(IIa)中,(X)和(XI),其中X <2>中,X <5>中,X <6>,R <9>和R <10>具有说明书中给出的含义。 式(XI)和它们的盐和酸加成物的化合物适用于通过不希望的微生物保护植物免受攻击。