![]() Method of sterilization of male anthers of plants
专利摘要:
A method of sterilising the male anthers of a plant, which comprises applying to the plant an azetidine derivative which is an acid of the general formula I or a salt and/or an ester, amide, alkylamide, hydrazide or alkylhydrazide thereof: …<CHEM>… in which:… X represents one of the groups CH2, CHR or CR2;… Y represents one of the groups CHR, CR2 or CH.CO2H;… Z represents one of the groups CH2, CHR, CR2 or CH.CO2H;… the or each R independently represents an alkyl, alkenyl or cycloalkyl group or an aryl or aralkyl group optionally substituted on the aryl nucleus by one or more of the same or different substituents selected from halogen atoms, alkyl groups and alkoxy groups;… and one but only one of Y and Z must represent a CH.CO2H group. 公开号:SU1500143A3 申请号:SU803005550 申请日:1980-11-13 公开日:1989-08-07 发明作者:Рой Джон Девлин Барри 申请人:Шелл Интернэшнл Рисерч Маатсхаппий Б.В. (Фирма); IPC主号:
专利说明:
The invention relates to agriculture, more specifically to breeding and seed production, and is associated with the sterilization of male anthers of plants using chemical means, gametocides. The purpose of the invention is to increase gametocidal activity. To obtain a high level of male sterility, it has been proposed to use 3-β-carboxyazetidine as a gametocide at a dose of 0.4-0.8 kg / ha. The treatment process is carried out when the plant is at the growth stage between late branching or tillering and the appearance of an ear. Biolot, the active substance can be used in the form of a composition with a solid or liquid carrier, surface-active agent. Example 1. Preparation of 3-carboxyazetidine. 1-Diphenylmethyl-3-cyanoazetidine (15 g, 0.06 mol) is mixed with 2-methoxyethanol (150 ml) and 13 g (0.2 mol) of potassium hydroxide in 10 ml of water is added to the solution. The mixture was heated under reflux for 15 hours and then poured into ice-water (1500 ml). The mixture is acidified with dilute hydrochloric acid to pH 1.5 and extracted with dichloromethane. Solid sodium bicarbonate is added to the aqueous phase to pH 1.5. The precipitate is filtered off, washed with water and air dried. 13 g (81%) of 1-diphenylmethyl-3-carboxyazetidine are obtained, m.p. 190-191 C (with. Decomposition). cl four SAE CM 5150 Calculated,%: C 76.4; H 6.4; N5,2. C ,, II, NO, Found .-),%: C 75.4; H 6.4; N5.1. The resulting product (10 g, 0.037 mol) is suspended in methanol (300 ml) and hydrogenated in the presence of palladium (II) hydroxide on coal for 3 h under a pressure of 3.5 atm. The solution is filtered under reduced pressure. The aqueous residue is extracted several times with dichloromethane, and then evaporated to dryness. The white residue is recrystallized from ethanol to obtain 2.6 g of shiny plates with mp. 169-170 ° C (with decomposition). Calculated,%: C 40.3; H 7.5; N 11.7. .0 Found,%: C 40.3; H 6.7; N 11.6 By evaporation of the recrystallization solvent, 1.2 g of crystals with a mp. 235-270 ° С (s. Decomposition). These crystals are anhydrous 3-carboxyazetidine. The overall yield is 92%. Example 2. Spring wheat Sicco varieties are grown in a greenhouse in 13 cm pots containing compost based on clay and sand with humus. Known compound of formula (I) ShR2 injected into a water solution containing 0.1% P 40 (torp grade) as a wetting agent and 1% acetone to improve solubility. The composition with water is adjusted to a concentration of 1000 ppm. and spray the plants with it before rolling. Plants are sprayed at this growth stage when the second node is visible. When spikes appear, but before pollination, 5 ears from each treated plant are placed in cellophane bags to prevent cross-flow. Upon reaching ripeness, the ears, placed in bags, are threshed and the number of seeds in them is counted, comparing with 0 five five five Q 0 five 0 0 34 untreated control ears. The results of the activity of compound (I) are given in Table. one. The compound (I) provides a degree of sterilization of 82%. Example 3. Barley. Barley commercial varieties Mazurka vfashvayut in the greenhouse, 13 cm pots containing compost based on loamy soil. The temperature is maintained at about 20 ° C. The compound obtained in Example 1 was introduced into an aqueous solution containing 0.1% nonidate P, 40 (trademark) as a wetting agent and 1% acetone to improve solubility. The composition is applied on a barley at a dose of 1.2 kg / ha when the leaf tab is shown, spraying the plant with it before draining. When spikes appear, 5 spikes from each pot are placed in cellophane bags to prevent cross-cutting. After ripening, the ears placed in bags are threshed and the number of grains is counted, comparing it with the untreated control group. The compound of example 1. The decrease in the number of grains formed (% of control) is 98.4%. Example 9. Corn. Corn commercial variety Inra 260 is grown in a greenhouse in 13 cm pots containing loamy-based compost. The temperature is maintained at about 25 ° C. The compound of Example 2 is introduced into a 0.5% solution of Tween 20 (trade mark) in distilled water, which is used as a surfactant. The composition is applied to plants for spraying leaves at a dose of 4 kg / ha before draining. The plants are sprayed in a stage with 11 leaves. Then the plants do not touch until the appearance of panicles, of which just about the next thing should be added. At this stage, the panicles are removed and the pollen is collected in separate fat-tight bags. The pollen collected from the treated plants is then transferred to silk (i.e., to female reproductive sites) of untreated plants. Silk is placed in sacks to prevent any random pollen from being pollinated. The level of induced male sterility is determined by counting the number of grains after ripening. The decrease in the number of grains formed (% of control) is 83.2%. Example 5. Winter wheat, a species of Aquila, is sown on the fields in Kent, suitable for the production of cereals, and is grown under normal cereal farming regimes. Plots with an area of 1.2 - 10 m are treated at various doses of consumption with 3-carboxyazetidine, and the treatment areas are divided by untreated squeezer areas of approximately the same size. The treatment is carried out at an early stage of booting. By dissolving the compound in water containing 0.75% v / v Mystery 20 as a wetting agent, using flat fan nozzles and with a volume of application of either 500 or 1000 l / ha. When an ear appears, but before flowering or puffing, the panicles on the selected processing plots are placed in cellophane bags to prevent cross-pollination. When maturity is reached, the spike with the kazvda of the treated plots is collected, the number of seeds is recorded and compared with the untreated control plots. The results are presented in table. 1, as well as at doses within the range of this interval. From tab. 1 it follows that the test compound causes sterility of the anthers at doses of both 0.4 and 3.2 kg / ha and also at doses that are in the interval of this interval. The ability of female cells to fertilize in treated plants remains high.
权利要求:
Claims (1) [1] Invention Formula A method of sterilizing male anthers of wheat plants, including them. treatment with the active substance, characterized in that, in order to increase the gametocidal activity, 3-carbsiazetidine in a dose is used as the active substance 0.4-0.8 kg / ha, I. Table 1 15 ZO 2a ZO ZO 25 table 2 35
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同族专利:
公开号 | 公开日 DD154272A5|1982-03-10| GR71932B|1983-08-19| RO92199B|1987-12-01| ZA807019B|1981-11-25| IE802360L|1981-05-16| US4560401A|1985-12-24| BR8007400A|1981-05-26| EP0029265A2|1981-05-27| PL227810A1|1981-12-23| JPS5688727A|1981-07-18| PH17449A|1984-08-29| EP0029265A3|1981-06-10| CA1261858A|1989-09-26| EP0029265B1|1983-08-17| AU539987B2|1984-10-25| HU188141B|1986-03-28| US4555260A|1985-11-26| DE3064597D1|1983-09-22| CS770280A2|1985-08-15| MX6618E|1985-08-23| OA06649A|1981-09-30| IE50474B1|1986-04-30| DK155772C|1989-10-02| NZ195544A|1983-05-10| DK155772B|1989-05-16| AT4437T|1983-08-15| ES8200868A1|1981-11-16| AU6433980A|1981-05-21| AR227653A1|1982-11-30| IL61480A|1984-09-30| TR20679A|1982-04-26| ES496798A0|1981-11-16| DK485280A|1981-05-17| RO92199A|1987-11-30| US4755210A|1988-07-05| JPH0130447B2|1989-06-20| MA18996A1|1981-07-01| PL125937B1|1983-06-30| IL61480D0|1980-12-31| CS243456B2|1986-06-12| EG15077A|1985-12-31|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 GB1567153A|1975-09-16|1980-05-14|Shell Int Research|Method of sterilizing male anthers of angiosperms| US4534787A|1984-05-24|1985-08-13|Shell Oil Company|N-L-seryl-3-azetidinecarboxylic acid|GB8300860D0|1983-01-13|1983-02-16|Shell Int Research|Azetidine compounds| GB8301702D0|1983-01-21|1983-02-23|Shell Int Research|Azetidine compounds| GB2140003A|1983-04-13|1984-11-21|Shell Int Research|Azetidine derivatives suitable for inducing male sterility in plants| GB8328253D0|1983-10-21|1983-11-23|Shell Int Research|Substituted azetidine derivatives| GB8412814D0|1984-05-18|1984-06-27|Shell Int Research|1-substituted azetidine-3-ol derivatives| US4534787A|1984-05-24|1985-08-13|Shell Oil Company|N-L-seryl-3-azetidinecarboxylic acid| EP0168852B1|1984-06-19|1989-07-26|Shell Internationale Researchmaatschappij B.V.|Azetidine derivatives and their preparation| GB8415615D0|1984-06-19|1984-07-25|Shell Int Research|Preparing azetidine derivatives| GB8419084D0|1984-07-26|1984-08-30|Shell Int Research|Azetidine derivatives| GB8419085D0|1984-07-26|1984-08-30|Shell Int Research|Azetidine derivatives| GB8514075D0|1985-06-04|1985-07-10|Shell Int Research|Therapeutic compounds| GB8627493D0|1986-11-18|1986-12-17|Shell Int Research|Catalytic hydrogenolysis| US4990504A|1987-07-17|1991-02-05|Fidia-Georgetown Institute For The Neurosciences|Azetidine derivatives to treat memory and learning disorders| US4946839A|1987-07-17|1990-08-07|Fidia-Georgetown Institute For The Neurosciences|Azetidine derivatives, compositions and methods of treating| DE3918990A1|1989-06-10|1990-12-13|Zeiss Carl Fa|MICROSCOPE WITH IMAGE BRIGHTNESS COMPENSATION| US5129940A|1991-08-22|1992-07-14|Orsan|Pollen suppressant for liliopsida plants comprising a 5-oxy-substituted cinnoline| KR100592798B1|2004-10-01|2006-06-26|한국화학연구원|Composition for control of harmful algae and dukweed comprising azetidine derivatives| US7348736B2|2005-01-24|2008-03-25|Philips Solid-State Lighting Solutions|Methods and apparatus for providing workspace lighting and facilitating workspace customization| US20060277618A1|2005-06-06|2006-12-07|Dairyland Seed Co., Inc.|Methods for producing a hybrid seed product| CN108069889B|2016-11-10|2021-10-01|上海西浦医药科技有限公司|Synthesis method of azetidine-3-formic acid|
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