or their acid-additive salts where: R1 or each R1 means independently optional substituted alkyl, cycloalkyl, cycloalkylalkyl, alkoxy, cycloalkoxy, alkoxyalkyl, aralkyl, aryl or aryloxy-group, or R1 and each R1 together with ring to which they were bound mean optional the substituted polycyclic hydrocarbon group; R2 means hydrogen atom or C1-4-alkyl group; R3 means hydrogen atom, hydroxy-group optional substituted with alkoxy- or acylhydroxy-group; R4 and R5 each independently means hydrogen atom, optional substituted alkyl, alkenyl, alkynyl, cycloalkylalkyl, cycloalkyl, bicycloalkyl, tricycloalkyl, alkoxyalkyl, aryl, aralkyl, haloidalkyl, 4-6-membered heterocyclic, tetrahydrofurfuryl or dioxolanyl group, or R4 and R5 together mean optional substituted suturated or unsaturated carbon chain that can contain optional one or more oxygen atoms and can be optional aryl or cycloalkyl fused ring; m = 0-6 and p = 0-3. Invention relates to synthesis of above indicated spiroheterocyclic compounds, intermediate compounds synthesized, compositions containing these compounds and their use as fungicides for phytopatogenic fungi control. EFFECT: improved method of synthesis."/> FUNGICIDIC SPIROHETEROCYCLIC DERIVATIVES AND THEIR ACID-ADDITIVE SALTS, METHOD OF SYNTHESIS, FUNGICIDIC COMPOSITION AND METHOD OF FUNGI CONTROL
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FUNGICIDIC SPIROHETEROCYCLIC DERIVATIVES AND THEIR ACID-ADDITIVE SALTS, METHOD OF SYNTHESIS, FUNGICIDIC COMPOSITION AND METHOD OF FUNGI CONTROL

机译:真菌孢子微环衍生物及其酸添加剂盐,合成方法,真菌组成和真菌控制方法

摘要

FIELD: organic chemistry. SUBSTANCE: product: new spiroheterocyclic compounds of the general formula (I): or their acid-additive salts where: R1 or each R1 means independently optional substituted alkyl, cycloalkyl, cycloalkylalkyl, alkoxy, cycloalkoxy, alkoxyalkyl, aralkyl, aryl or aryloxy-group, or R1 and each R1 together with ring to which they were bound mean optional the substituted polycyclic hydrocarbon group; R2 means hydrogen atom or C1-4-alkyl group; R3 means hydrogen atom, hydroxy-group optional substituted with alkoxy- or acylhydroxy-group; R4 and R5 each independently means hydrogen atom, optional substituted alkyl, alkenyl, alkynyl, cycloalkylalkyl, cycloalkyl, bicycloalkyl, tricycloalkyl, alkoxyalkyl, aryl, aralkyl, haloidalkyl, 4-6-membered heterocyclic, tetrahydrofurfuryl or dioxolanyl group, or R4 and R5 together mean optional substituted suturated or unsaturated carbon chain that can contain optional one or more oxygen atoms and can be optional aryl or cycloalkyl fused ring; m = 0-6 and p = 0-3. Invention relates to synthesis of above indicated spiroheterocyclic compounds, intermediate compounds synthesized, compositions containing these compounds and their use as fungicides for phytopatogenic fungi control. EFFECT: improved method of synthesis.
机译:领域:有机化学。物质:产品:通式(I)的新型螺杂环化合物:或它们的酸-添加剂盐,其中:R 1 或每个R 1 分别独立表示任选取代的烷基,环烷基,环烷基烷基,烷氧基,环烷氧基,烷氧基烷基,芳烷基,芳基或芳氧基或 1 和每个R 1 以及与它们相连的环是指取代的多环烃基; R 2 是指氢原子或C 1-4 -烷基; R 3 是指氢原子,任选被烷氧基或酰基羟基取代的羟基; R 4 和R 5 分别独立地是指氢原子,任选取代的烷基,烯基,炔基,环烷基烷基,环烷基,双环烷基,三环烷基,烷氧基烷基,芳基,芳烷基,卤代烷基,4 -6元杂环,四氢糠基或二氧戊环基或R 4 和R 5 一起表示可取代的取代的饱和或不饱和碳链,可包含一个或多个氧原子;可以是任选的芳基或环烷基稠环; m = 0-6,p = 0-3。本发明涉及上述螺杂环化合物的合成,合成的中间体化合物,含有这些化合物的组合物及其作为控制植物病原真菌的杀真菌剂的用途。效果:改进的合成方法。

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