5-Aminomethyl-1,3-oxathiolane microbicides, compositions and use
    121.
    发明授权
    5-Aminomethyl-1,3-oxathiolane microbicides, compositions and use 失效
    5-氨基甲基-1,3-氧硫杂环戊烷杀微生物剂,组合物和用途

    公开(公告)号:US4542130A

    公开(公告)日:1985-09-17

    申请号:US624889

    申请日:1984-06-27

    摘要: MIcrobicidally active 5-aminomethyl-1,3-oxathiolanes of the formula ##STR1## in which R.sup.1 is tetrahydronaphthyl, decahydronaphthyl or optionally substituted naphthyl, optionally substituted cycloalkyl or cycloalkenyl, optionally substituted phenyl, or alkyl which is substituted by phenyl, phenoxy, phenylthio, cyclohexyl, cyclohexyloxy or cyclohexylthio, each of which is optionally substituted,R.sup.2 is hydrogen or methyl,R.sup.3 is alkyl, andR.sup.4 is alkyl, alkenyl or optionally substituted aralkyl, orR.sup.3 and R.sup.4, together with the nitrogen atom to which they are bonded, form an optionally substituted saturated heterocyclic structure which can contain further heteroatoms,or a plant-tolerated addition product thereof with an acid or metal salt.

    摘要翻译: 其中R 1为四氢萘基,十氢萘基或任选取代的萘基,任选取代的环烷基或环烯基,任选取代的苯基,或被苯基,苯氧基,苯硫基取代的烷基的除草活性的5-氨基甲基-1,3-氧硫杂环戊烷 环己基,环己氧基或环己基硫基,其各自任选被取代,R 2是氢或甲基,R 3是烷基,R 4是烷基,烯基或任选被取代的芳烷基,或者R 3和R 4与它们所键合的氮原子一起 形成可以含有其它杂原子的任选取代的饱和杂环结构,或其含有酸或金属盐的植物耐受的加成产物。

    Fungicidal agents
    122.
    发明授权
    Fungicidal agents 失效
    杀真菌剂

    公开(公告)号:US5240952A

    公开(公告)日:1993-08-31

    申请号:US885417

    申请日:1992-05-19

    摘要: A fungicidal composition comprising a fungicidally effective amount of (i) a substituted 1-hydroxyethyl-triazole of the formula ##STR1## in which A is --CH.sub.2 CH.sub.2 -- or --CH.dbd.CH--,or an addition product thereof with an acid or metal salt, and (ii) at least one member selected from the group consisting ofA) wettable sulphur,B) a polyhalogenoalkylthio derivative,C) a guanidine derivative,D) an aromatic carboxylic acid derivative,E) a dithocarbamate,F) a benzimidazole derivative,G) an imidazole or triazole derivative,H) a phosphoric acid ester,I) a tetrahydroquinoline derivative,J) an S,N-heterocyclene compound,K) a urea derivative,L) a sulphonamide derivative,M) a polyhydroxy ether derivative,N) a triazine derivative,O) a copper complex salt,P) an N-formyl derivative,Q) a morpholine derivative,R) a quinoxaline derivative, andS) a dicarboximide derivative.

    摘要翻译: 一种杀真菌组合物,其包含杀真菌有效量的(i)其中A是-CH 2 CH 2 - 或-CH = CH-的式“IMAGE”的取代的1-羟乙基三唑或其与酸或金属盐的加成产物 ,和(ii)至少一种选自A)可湿性硫,B)多卤代烷硫基衍生物,C)胍衍生物,D)芳族羧酸衍生物,E)二氨基甲酸酯,F)苯并咪唑衍生物 ,G)咪唑或三唑衍生物,H)磷酸酯,I)四氢喹啉衍生物,J)S,N-杂环烯化合物,K)脲衍生物,L)磺酰胺衍生物,M)多羟基醚衍生物 ,N)三嗪衍生物,O)铜络合盐,P)N-甲酰基衍生物,Q)吗啉衍生物,R)喹喔啉衍生物和S)二羧酰亚胺衍生物。

    Heterocyclic amide derivatives
    126.
    发明授权
    Heterocyclic amide derivatives 失效
    杂环酰胺衍生物

    公开(公告)号:US4840961A

    公开(公告)日:1989-06-20

    申请号:US851057

    申请日:1986-04-11

    摘要: Novel heterocyclic amide derivatives of the formula ##STR1## in which R.sup.1 represents alkyl, or represents alkenyl which has more than 2 carbon atoms and is optionally substituted by halogen, or represents alkinyl which has more than 2 carbon atoms and is optionally substituted by halogen, or represents alkoxyalkyl or alkylthioalkyl;R.sup.2 represents optionally substituted naphthyl, or represents optionally substituted tetrahydronaphthyl, or represents optionally substituted indanyl;A represents an alkylene bridge, or also an alkenylene bridge if X denotes a direct bond;X represents oxygen, sulphur or a direct bond;Y represents oxygen or sulphur;B represents imidazol-1-yl, pyridin-3-yl, pyrazin-2-yl, pyrimidin-5-yl, 1,2,4-triazol-1-yl or 1-methyl-imidazol-5-yl-;and their acid addition salts and metal salt complexes, are outstandingly active as fungicides.

    摘要翻译: 式(I)的新型杂环酰胺衍生物,其中R 1表示烷基,或表示具有多于2个碳原子并且任选被卤素取代的烯基,或表示具有多于2个碳原子并且任选被取代的炔基 或代表烷氧基烷基或烷硫基烷基; R 2表示任选取代的萘基,或表示任选取代的四氢萘基,或表示任选取代的茚满基; A表示亚烷基桥,或者如果X表示直接键,则表示亚烯基桥; X表示氧,硫或直接键; Y表示氧或硫; B表示咪唑-1-基,吡啶-3-基,吡嗪-2-基,嘧啶-5-基,1,2,4-三唑-1-基或1-甲基 - 咪唑-5-基 - 和它们的酸加成盐和金属盐络合物,作为杀真菌剂具有突出的活性。