![]() Method of controlling undesirable vegetation
专利摘要:
公开号:SU1209016A3 申请号:SU823456151 申请日:1982-05-27 公开日:1986-01-30 发明作者:Бекер Райнер;Ян Дитер;Рор Вольфганг;Химмеле Вальтер;Зигель Хардо;Вюрцер Бруно 申请人:Басфаг (Фирма); IPC主号:
专利说明:
This invention relates to chemical methods for controlling weeds and undesirable vegetation by treating it or the soil on which it grows with herbicides. The purpose of the invention is to increase the efficiency of a method for controlling undesirable vegetation based on the use of cyclohexanedione derivatives. In tab. 1 shows the active substances - derivatives of cyclohexanedione - and specific examples illustrating the effectiveness of the proposed method. The active ingredients of the general formula exist in three different tautomeric forms. to ABOUT - he Oli R -a z 0 with p ok R The compounds of the general formula are used in conventional formulations: solutions, powders, granules, emulsions, dispersions, dusts. They are prepared by common methods in the preparation of preparative forms of pesticides. Example 1. Pre-emergence treatment. Seeds of experimental plants were sown in prepared soil, placed in special pots, and immediately after that, the soil was treated with active substances in the form of an aqueous emulsion or dispersion. Then the pots were rolled with transparent plastic caps and the plants were grown for 2-4 weeks. Evaluation of the herbicidal effect was carried out on a scale from 0 to 100: O - no effect; 100 - full of death of plants. 2Propyl Allyl 3Propyl Allyl 2- (1,3-Dispsan-2-yl) ethyl 2- (1, 3-Dithiolan-2-yl) ethyl The results of the experiments are presented in table. 2 Example 2. Post-harvest processing. Experimental plants grown under greenhouse conditions up to stale 3–15 cm were treated with active substances in the form of aqueous emulsions or dispersions and 2–4 weeks after treatment, the herbicidal effect was evaluated according to the scale described in Example 1. The results of the experiments are presented in table. 3-9. Example 3. Post-harvest field experience. Young small winter rapeseed was grown on small field businesses and post-emergence treatment of these sites was carried out in order to combat weed barley. The results of the experiment are presented in table. ten. Table 1 Hydrogen Methoxycarbonyl Continued tabl, 1 - dihydrothiopyran-3-yl Hydrogen as sodium salt. Continuation of table 1 . Table 2 Herbicidal effect in pre-emergence treatment under greenhouse conditions at a dose of 3 kg / ha 9.120901610 Table 3 Herbicidal effect 4) ect with post-emergence treatment under greenhouse conditions at a dose of 0.25 kg / ha ABOUT about SzN7 Table 4 Herbicidal effect in post-harvest treatment in greenhouse conditions Continuation of table 4 Table 6 Herbicidal effect of prc post-harvest treatment. Treatment in hepatitis C: Hep: face at a dose of 0.25 kg / ha Table 7 Herbicidal effect in post-harvest treatment under conditions th .0 Dose 0.25 kg / ha Table 8 Herbicidal effect in post-harvest treatment in greenhouse conditions 17120901618 Continuation of table 9 Experimental plants and herbicidal effect Wild Oat Chaff Ezhovnik 100 100 100 100 100 100 -. 100 100 Table 10 bicidal effect during post-harvest processing in field experience Dose, Experimental plants, herbicidal kg / hee , . Rapeseed Barley 025 Qgg R “Ogg . t .H1. ", ...." ",". "... .b. ".. p, N", ... „„ N. . . to, VYA ".." -... "..." ,. „“ .. : Compiled by R. Streltsov Editor N. Dolinich Tehred M. Parotsay Proofreader T. Kolba Order 302/61 Circulation 679 Subscription VNIIPI USSR State Committee for inventions and discoveries 113035, Moscow, Zh-35, Raushsk nab., 4/5 Branch PPP Patent, Uzhgorod, Proektna St., 4
权利要求:
Claims (1) [1] METHOD FOR FIGHTING UNWANTED VEGETATION by treating it or the soil on which it grows with cyclohexanedione derivatives, characterized in that, in order to increase the efficiency of the method, a compound of the general formula is used as cyclohexanedione derivatives where R 'is methyl, ethyl, propyl; • R 2 - ethyl, allyl, 2-chlorallyl, propargyl; R is tetrahydropyran-2-yl, tetrahydropyran-3-yl, 4-methyltetrahydropyran-3-yl, (2H) ~ -5,6-dihydropyran-3-yl, (4H) -2,5-dimethyl-2,3 -dihydropyran-2-yl, (4H) -2,3-dihydropyran-2-yl, tetrahydropyr an-4-yl-me type, tetrahydropyran-2-yl-methyl, 2- (1,3-dioxan-2- il) ethyl, 2- (1,3-dithiolan-2-yl) -ethyl, 1- (4-methyl-1,3-dioxan-2-yl) -2methylpropyl, tetrahydrothiopyran-3-yl, (2H) - 5,6-dihydrothiopyran-3-yl, (2H) -2,6-dimethip-5,6-dihydropyran-3-yl, (2H) -2,6-dimethyl-5,6-dihydrothiopyran-3-yl; Z is hydrogen or methoxycarbonyl; or its sodium salt in an amount of 0.125-3 kg / ha. SU „1209016
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引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US3950420A|1973-08-15|1976-04-13|Nippon Soda Company, Ltd.|Cyclohexane derivatives| JPS5521001B2|1973-08-15|1980-06-06| JPS577122B2|1973-12-24|1982-02-09| JPS5811841B2|1974-06-04|1983-03-04|Nippon Soda Co| JPS6011006B2|1974-07-25|1985-03-22|Nippon Soda Co| JPS5931481B2|1974-09-20|1984-08-02|Nippon Soda Co| DE3121355A1|1981-05-29|1982-12-16|Basf Ag, 6700 Ludwigshafen|CYCLOHEXANDION DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND HERBICIDES CONTAINING THEM| JPS6113756A|1984-06-28|1986-01-22|Konishiroku Photo Ind Co Ltd|Image forming method|USRE32489E|1980-11-25|1987-09-01|Chevron Research Company|Herbicidal substituted 2--alkylidene)-cyclohexane-1,3-diones| DE3121355A1|1981-05-29|1982-12-16|Basf Ag, 6700 Ludwigshafen|CYCLOHEXANDION DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND HERBICIDES CONTAINING THEM| DE3230087A1|1982-08-13|1984-02-16|Basf Ag, 6700 Ludwigshafen|CYCLOHEXAN-1,3-DION DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| ZA836241B|1982-09-02|1985-03-27|Ici Australia Ltd|Herbicidal cyclohexane-1,3-dione derivatives| DE3239071A1|1982-10-22|1984-04-26|Basf Ag, 6700 Ludwigshafen|CYCLOHEXAN-1,3-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR COMBATING UNWANTED PLANT GROWTH| DE3303182A1|1983-02-01|1984-08-02|Basf Ag, 6700 Ludwigshafen|CYCLOHEXAN-1,3-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR COMBATING UNWANTED PLANT GROWTH| DE3310418A1|1983-03-23|1984-09-27|Basf Ag, 6700 Ludwigshafen|CYCLOHEXAN-1,3-DION, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| NZ207964A|1983-05-06|1987-03-31|Ici Australia Ltd|5-heteroaryl-cyclohexane-1,3-dione derivatives| EP0126713B1|1983-05-18|1989-01-18|Ciba-Geigy Ag|Cyclohexanedione-carboxylic-acid derivatives having a herbicidal and plant growth regulating activity| US4544399A|1983-07-01|1985-10-01|Stauffer Chemical Company|Certain 1,3-cyclohexanedione adducts of substituted phenoxyphenoxypropionic acids and their use as an herbicide| DE3324707A1|1983-07-08|1985-01-17|Basf Ag, 6700 Ludwigshafen|CYCLOHEXAN-1,3-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR COMBATING UNWANTED PLANT GROWTH| DE3333678A1|1983-09-17|1985-03-28|Basf Ag, 6700 Ludwigshafen|METHOD FOR PRODUCING 3-FORMYL-TETRAHYDROTHIOPYRANES| DE3412794A1|1983-09-30|1985-04-18|Basf Ag, 6700 Ludwigshafen|CYCLOHEXENON DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| IL73152D0|1983-10-05|1985-01-31|Basf Ag|Cyclohexenol derivatives and their use as herbicides| DE3340265A1|1983-11-08|1985-05-15|Basf Ag, 6700 Ludwigshafen|CYCLOHEXAN-1,3-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR COMBATING UNWANTED PLANT GROWTH| DE3429437A1|1983-12-08|1985-06-20|Basf Ag, 6700 Ludwigshafen|CYCLOHEXENON DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| DE3410492A1|1984-03-06|1985-09-12|Basf Ag, 6700 Ludwigshafen|CYCLOHEXANONE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| DE3430229A1|1984-03-29|1985-10-10|Basf Ag, 6700 Ludwigshafen|CYCLOHEXENON DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| DE3421351A1|1984-06-08|1985-12-12|Bayer Ag, 5090 Leverkusen|SUBSTITUTED TETRAHYDROTHIOPYRAN-2,4-DIONE| DE3437238A1|1984-10-11|1986-04-17|Basf Ag, 6700 Ludwigshafen|NEW COMPOUNDS, METHOD FOR THEIR PRODUCTION AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| DE3536117A1|1985-10-10|1987-04-16|Basf Ag|CYCLOHEXENON DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| DE3543447A1|1985-12-09|1987-06-11|Basf Ag|CYCLOHEXENON DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS HERBICIDES AND REGULATING AGENTS| DE3600642A1|1986-01-11|1987-07-16|Basf Ag|CYCLOHEXENON DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS AN HERBICIDE AGENT| DE3601066A1|1986-01-16|1987-07-23|Basf Ag|CYCLOHEXENON DERIVATIVES, A METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS HERBICIDES AND REGULATIVE AGENTS FOR REGULATING THE PLANT| DE3609181A1|1986-03-19|1987-09-24|Basf Ag|CYCLOHEXENON DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR CONTROLLING UNWANTED PLANT GROWTH| JP2784920B2|1988-01-29|1998-08-13|日本農薬株式会社|1,3-cyclohexanedione derivative| DE4227896A1|1992-08-22|1994-02-24|Basf Ag|Cyclohexenone oxime ethers, their preparation and their use| DE4427995A1|1994-08-08|1996-02-15|Basf Ag|Saccharin derivatives| EP1382247A1|2002-07-18|2004-01-21|Bayer CropScience GmbH|Combinations of cyclohexanedione oxime herbicides and safeners| EP2052605A1|2007-10-24|2009-04-29|Bayer CropScience AG|Herbicide combination| DE102008037632A1|2008-08-14|2010-02-18|Bayer Cropscience Ag|Herbicide combination with dimethoxytriazinyl-substituted difluoromethanesulfonylanilides|
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申请号 | 申请日 | 专利标题 DE19813121355|DE3121355A1|1981-05-29|1981-05-29|CYCLOHEXANDION DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND HERBICIDES CONTAINING THEM| 相关专利
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