NO841567L - Fremgangsmaate til fremstilling av haploide froe og dupolider og homozygote planteslekter av disse - Google Patents
Fremgangsmaate til fremstilling av haploide froe og dupolider og homozygote planteslekter av disseInfo
- Publication number
- NO841567L NO841567L NO841567A NO841567A NO841567L NO 841567 L NO841567 L NO 841567L NO 841567 A NO841567 A NO 841567A NO 841567 A NO841567 A NO 841567A NO 841567 L NO841567 L NO 841567L
- Authority
- NO
- Norway
- Prior art keywords
- alkyl
- group
- oxo
- dihydro
- hydrogen atom
- Prior art date
Links
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- 238000002360 preparation method Methods 0.000 title description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 78
- 239000003795 chemical substances by application Substances 0.000 claims description 70
- 241000196324 Embryophyta Species 0.000 claims description 66
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 57
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 34
- -1 alkaline earth metal cation Chemical class 0.000 claims description 30
- 150000001875 compounds Chemical class 0.000 claims description 26
- 125000005843 halogen group Chemical group 0.000 claims description 26
- 239000001257 hydrogen Substances 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 22
- 150000003839 salts Chemical class 0.000 claims description 22
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 19
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- 239000011734 sodium Substances 0.000 claims description 19
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- 125000003545 alkoxy group Chemical group 0.000 claims description 14
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- 238000011161 development Methods 0.000 claims description 12
- 230000018109 developmental process Effects 0.000 claims description 12
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
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- 125000003118 aryl group Chemical group 0.000 claims description 8
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- 230000021121 meiosis Effects 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
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- 125000004434 sulfur atom Chemical group 0.000 claims description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
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- OFLOYPFFDFJFSW-UHFFFAOYSA-N ethyl 2-(4-chlorophenyl)-3-ethyl-5-oxopyridazine-4-carboxylate Chemical compound N1=CC(=O)C(C(=O)OCC)=C(CC)N1C1=CC=C(Cl)C=C1 OFLOYPFFDFJFSW-UHFFFAOYSA-N 0.000 claims description 3
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- KSKLALWRZFODIU-UHFFFAOYSA-N methyl 1-(4-chlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound CCC1=CC(=O)C(C(=O)OC)=NN1C1=CC=C(Cl)C=C1 KSKLALWRZFODIU-UHFFFAOYSA-N 0.000 description 1
- CKURQPUVUUYRPH-UHFFFAOYSA-N methyl 1-(4-iodophenyl)-6-methyl-4-oxopyridazine-3-carboxylate Chemical compound CC1=CC(=O)C(C(=O)OC)=NN1C1=CC=C(I)C=C1 CKURQPUVUUYRPH-UHFFFAOYSA-N 0.000 description 1
- YAIRSPHHLGCRNO-UHFFFAOYSA-N methyl 2-(4-chlorophenyl)-3-ethyl-5-oxopyridazine-4-carboxylate Chemical compound CCC1=C(C(=O)OC)C(=O)C=NN1C1=CC=C(Cl)C=C1 YAIRSPHHLGCRNO-UHFFFAOYSA-N 0.000 description 1
- LEFHKCWENBVSFU-UHFFFAOYSA-N methyl 5-acetyl-1-(4-chlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound CCC1=C(C(C)=O)C(=O)C(C(=O)OC)=NN1C1=CC=C(Cl)C=C1 LEFHKCWENBVSFU-UHFFFAOYSA-N 0.000 description 1
- NYGDNNQNJLGEBF-UHFFFAOYSA-N methyl 6-bromo-2-(4-chlorophenyl)-3-ethyl-5-oxopyridazine-4-carboxylate Chemical compound CCC1=C(C(=O)OC)C(=O)C(Br)=NN1C1=CC=C(Cl)C=C1 NYGDNNQNJLGEBF-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 229920003087 methylethyl cellulose Polymers 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- 229960001730 nitrous oxide Drugs 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000006916 nutrient agar Substances 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 230000008121 plant development Effects 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229960003975 potassium Drugs 0.000 description 1
- 235000007686 potassium Nutrition 0.000 description 1
- RWPGFSMJFRPDDP-UHFFFAOYSA-L potassium metabisulfite Chemical compound [K+].[K+].[O-]S(=O)S([O-])(=O)=O RWPGFSMJFRPDDP-UHFFFAOYSA-L 0.000 description 1
- 239000004297 potassium metabisulphite Substances 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- GURNAAYLUXBKGA-UHFFFAOYSA-M potassium;2-(4-chlorophenyl)-5-oxo-3-propylpyridazine-4-carboxylate Chemical compound [K+].CCCC1=C(C([O-])=O)C(=O)C=NN1C1=CC=C(Cl)C=C1 GURNAAYLUXBKGA-UHFFFAOYSA-M 0.000 description 1
- BVUOHHPFPZFYEW-UHFFFAOYSA-M potassium;5-(carboxymethyl)-1-(2-chlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(CC(O)=O)C(=O)C(C([O-])=O)=NN1C1=CC=CC=C1Cl BVUOHHPFPZFYEW-UHFFFAOYSA-M 0.000 description 1
- TXIBRVZDJXKLGE-UHFFFAOYSA-M potassium;5-(carboxymethyl)-1-(3,4-dichlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(CC(O)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(Cl)C(Cl)=C1 TXIBRVZDJXKLGE-UHFFFAOYSA-M 0.000 description 1
- KJGLQFDXBNIEBC-UHFFFAOYSA-M potassium;5-(carboxymethyl)-1-(4-chlorophenyl)-4-oxo-6-propylpyridazine-3-carboxylate Chemical compound [K+].CCCC1=C(CC(O)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(Cl)C=C1 KJGLQFDXBNIEBC-UHFFFAOYSA-M 0.000 description 1
- RZNADCSHBJYEFN-UHFFFAOYSA-M potassium;5-(carboxymethyl)-1-(4-chlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(CC(O)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(Cl)C=C1 RZNADCSHBJYEFN-UHFFFAOYSA-M 0.000 description 1
- RFKWRQQVNQSAJK-UHFFFAOYSA-M potassium;5-(carboxymethyl)-6-ethyl-1-(4-iodophenyl)-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(CC(O)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(I)C=C1 RFKWRQQVNQSAJK-UHFFFAOYSA-M 0.000 description 1
- SJVXIDLZFULOKO-UHFFFAOYSA-M potassium;5-acetyl-1-(4-bromophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(C(C)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(Br)C=C1 SJVXIDLZFULOKO-UHFFFAOYSA-M 0.000 description 1
- CHWOVEJUIPJPIS-UHFFFAOYSA-M potassium;5-acetyl-1-(4-chlorophenyl)-6-ethyl-4-oxopyridazine-3-carboxylate Chemical compound [K+].CCC1=C(C(C)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(Cl)C=C1 CHWOVEJUIPJPIS-UHFFFAOYSA-M 0.000 description 1
- DYFZDDSVXRLBQY-UHFFFAOYSA-M potassium;5-acetyl-6-ethyl-4-oxo-1-[4-(trifluoromethyl)phenyl]pyridazine-3-carboxylate Chemical compound [K+].CCC1=C(C(C)=O)C(=O)C(C([O-])=O)=NN1C1=CC=C(C(F)(F)F)C=C1 DYFZDDSVXRLBQY-UHFFFAOYSA-M 0.000 description 1
- FZNDOIGSABBARI-UHFFFAOYSA-M potassium;5-acetyl-6-ethyl-4-oxo-1-phenylpyridazine-3-carboxylate Chemical compound [K+].CCC1=C(C(C)=O)C(=O)C(C([O-])=O)=NN1C1=CC=CC=C1 FZNDOIGSABBARI-UHFFFAOYSA-M 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- IEPZHOPFBLVNFY-UHFFFAOYSA-N prop-1-enyl 1-(4-chlorophenyl)-6-methyl-4-oxopyridazine-3-carboxylate Chemical compound CC1=CC(=O)C(C(=O)OC=CC)=NN1C1=CC=C(Cl)C=C1 IEPZHOPFBLVNFY-UHFFFAOYSA-N 0.000 description 1
- JKANAVGODYYCQF-UHFFFAOYSA-N prop-2-yn-1-amine Chemical compound NCC#C JKANAVGODYYCQF-UHFFFAOYSA-N 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 210000001938 protoplast Anatomy 0.000 description 1
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 150000008318 pyrimidones Chemical class 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000008707 rearrangement Effects 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000010187 selection method Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000014639 sexual reproduction Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229960004249 sodium acetate Drugs 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229940083608 sodium hydroxide Drugs 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- NBNBICNWNFQDDD-UHFFFAOYSA-N sulfuryl dibromide Chemical compound BrS(Br)(=O)=O NBNBICNWNFQDDD-UHFFFAOYSA-N 0.000 description 1
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229950003937 tolonium Drugs 0.000 description 1
- HNONEKILPDHFOL-UHFFFAOYSA-M tolonium chloride Chemical compound [Cl-].C1=C(C)C(N)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 HNONEKILPDHFOL-UHFFFAOYSA-M 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 230000008736 traumatic injury Effects 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- GCRCSLNXFKCFHB-UHFFFAOYSA-N triethyl(hexyl)azanium Chemical compound CCCCCC[N+](CC)(CC)CC GCRCSLNXFKCFHB-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- WSFDRHZUAHDHDN-UHFFFAOYSA-N trimethyl-[(4-methylphenyl)methyl]azanium Chemical compound CC1=CC=C(C[N+](C)(C)C)C=C1 WSFDRHZUAHDHDN-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N61/00—Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
- A01H1/00—Processes for modifying genotypes ; Plants characterised by associated natural traits
- A01H1/02—Methods or apparatus for hybridisation; Artificial pollination ; Fertility
- A01H1/022—Genic fertility modification, e.g. apomixis
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Genetics & Genomics (AREA)
- Botany (AREA)
- Developmental Biology & Embryology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48888883A | 1983-04-26 | 1983-04-26 | |
| US58435884A | 1984-02-28 | 1984-02-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO841567L true NO841567L (no) | 1984-10-29 |
Family
ID=27049511
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO841567A NO841567L (no) | 1983-04-26 | 1984-04-18 | Fremgangsmaate til fremstilling av haploide froe og dupolider og homozygote planteslekter av disse |
Country Status (14)
| Country | Link |
|---|---|
| EP (1) | EP0127313B1 (cs) |
| AU (1) | AU562972B2 (cs) |
| BR (1) | BR8401899A (cs) |
| CA (1) | CA1236700A (cs) |
| DE (1) | DE3478985D1 (cs) |
| DK (1) | DK207184A (cs) |
| ES (1) | ES8605139A1 (cs) |
| GR (1) | GR79912B (cs) |
| HU (1) | HU191749B (cs) |
| IL (1) | IL71635A (cs) |
| NO (1) | NO841567L (cs) |
| NZ (1) | NZ207927A (cs) |
| PH (1) | PH23110A (cs) |
| PT (1) | PT78490B (cs) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4623378A (en) * | 1983-08-10 | 1986-11-18 | Ciba-Geigy Corporation | Gametocidal pyridazinylcarboxylic acid derivatives |
| FR2566995B1 (fr) * | 1984-07-04 | 1987-02-13 | Centre Nat Rech Scient | Procede de preparation d'haploides doubles de cereales. |
| DE3843199C2 (de) * | 1988-12-22 | 1998-03-12 | Nunhems Zaden Bv | Verfahren zur Herstellung von doppelt-haploiden Gurken |
| US6706989B2 (en) | 2001-02-02 | 2004-03-16 | Pioneer Hi-Bred International, Inc. | Automated high-throughput seed sample processing system and method |
| US7703238B2 (en) | 2004-08-26 | 2010-04-27 | Monsanto Technology Llc | Methods of seed breeding using high throughput nondestructive seed sampling |
| EP1786261B1 (en) | 2004-08-26 | 2014-04-30 | Monsanto Technology, LLC | Automated seed sampler and methods of sampling, testing and bulking seeds |
| US8028469B2 (en) | 2006-03-02 | 2011-10-04 | Monsanto Technology Llc | Automated high-throughput seed sampler and methods of sampling, testing and bulking seeds |
| US7998669B2 (en) | 2006-03-02 | 2011-08-16 | Monsanto Technology Llc | Automated contamination-free seed sampler and methods of sampling, testing and bulking seeds |
| CN103118527B (zh) | 2010-07-20 | 2016-06-08 | 孟山都技术有限公司 | 用于从种子去除组织样本的自动化系统以及相关方法 |
| US9677082B2 (en) | 2013-03-15 | 2017-06-13 | Syngenta Participations Ag | Haploid induction compositions and methods for use therefor |
| CA3000018A1 (en) * | 2015-11-18 | 2017-05-26 | Timothy Joseph KELLIHER | Haploid induction compositions and methods for use therefor |
| AU2017259702A1 (en) * | 2016-05-03 | 2018-12-13 | Basf Se | Applications of root-administered chemical hybridizing agents in plant breeding |
| USD1022462S1 (en) * | 2020-02-28 | 2024-04-16 | Rothy's, Inc. | Bag |
| GB202018994D0 (en) | 2020-12-02 | 2021-01-13 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| GB202018996D0 (en) | 2020-12-02 | 2021-01-13 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| MX2024007176A (es) | 2021-12-17 | 2024-06-26 | Syngenta Crop Protection Ag | Derivados herbicidas de piridona. |
| CN119095827A (zh) | 2022-04-27 | 2024-12-06 | 先正达农作物保护股份公司 | 除草2-氧代-烟酸衍生物 |
| IL317114A (en) | 2022-06-01 | 2025-01-01 | Syngenta Crop Protection Ag | Herbicide derivatives |
| AU2023281844A1 (en) | 2022-06-01 | 2024-12-05 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| JP2025523360A (ja) | 2022-06-01 | 2025-07-23 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 除草性誘導体 |
| AR130324A1 (es) | 2022-09-01 | 2024-11-27 | Syngenta Crop Protection Ag | Derivados herbicidas |
| CN120282950A (zh) | 2022-12-01 | 2025-07-08 | 先正达农作物保护股份公司 | 除草衍生物 |
| WO2024223510A1 (en) | 2023-04-27 | 2024-10-31 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| WO2025087845A1 (en) | 2023-10-23 | 2025-05-01 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| WO2025108824A1 (en) | 2023-11-21 | 2025-05-30 | Syngenta Crop Protection Ag | Herbicidal derivatives |
| WO2025119663A1 (en) | 2023-12-05 | 2025-06-12 | Syngenta Crop Protection Ag | Herbicidal derivatives |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4115101A (en) * | 1976-05-24 | 1978-09-19 | Rohm And Haas Company | 1-Aryl-4-pyridones |
| US4345934A (en) * | 1977-03-10 | 1982-08-24 | Rohm And Haas Company | Method of producing hybrid cereal grain seeds by application of 1-aryl-1,4-dihydro-4-oxo(thio)-pyridazines |
| EP0037133A1 (en) * | 1980-03-26 | 1981-10-07 | Shell Internationale Researchmaatschappij B.V. | Pyridazinone compounds, process for their preparation, compositions containing them and a method of regulating the growth of plants, increasing the yield of soya bean plants and sterilizing the male anthers of plants, including small grain cereal plants, using them as well as a method of producing F1 hybrid seed |
| EP0037134A1 (en) * | 1980-03-26 | 1981-10-07 | Shell Internationale Researchmaatschappij B.V. | Pyridazine derivatives, process for their preparation, compositions containing them and methods of regulating the growth of plants, increasing the yield of soya bean plants and sterilizing the male anthers of plants, including small grain cereal plants, using them as well as a method of producing F1 hybrid seed |
| AU539399B2 (en) * | 1980-05-12 | 1984-09-27 | Zeneca Limited | Substituted oxonicotinates |
-
1984
- 1984-04-12 CA CA000451846A patent/CA1236700A/en not_active Expired
- 1984-04-18 NO NO841567A patent/NO841567L/no unknown
- 1984-04-18 PH PH30579A patent/PH23110A/en unknown
- 1984-04-19 NZ NZ207927A patent/NZ207927A/en unknown
- 1984-04-24 ES ES531843A patent/ES8605139A1/es not_active Expired
- 1984-04-24 GR GR74481A patent/GR79912B/el unknown
- 1984-04-24 BR BR8401899A patent/BR8401899A/pt not_active Application Discontinuation
- 1984-04-25 HU HU841595A patent/HU191749B/hu not_active IP Right Cessation
- 1984-04-25 DK DK207184A patent/DK207184A/da not_active Application Discontinuation
- 1984-04-25 IL IL71635A patent/IL71635A/xx unknown
- 1984-04-25 EP EP84302772A patent/EP0127313B1/en not_active Expired
- 1984-04-25 DE DE8484302772T patent/DE3478985D1/de not_active Expired
- 1984-04-26 AU AU27272/84A patent/AU562972B2/en not_active Ceased
- 1984-04-26 PT PT78490A patent/PT78490B/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| IL71635A (en) | 1988-12-30 |
| DK207184D0 (da) | 1984-04-25 |
| DE3478985D1 (en) | 1989-08-24 |
| NZ207927A (en) | 1987-09-30 |
| AU562972B2 (en) | 1987-06-25 |
| BR8401899A (pt) | 1984-12-04 |
| ES531843A0 (es) | 1986-03-16 |
| CA1236700A (en) | 1988-05-17 |
| PT78490A (en) | 1984-05-01 |
| GR79912B (cs) | 1984-10-31 |
| HUT39061A (en) | 1986-08-28 |
| ES8605139A1 (es) | 1986-03-16 |
| EP0127313B1 (en) | 1989-07-19 |
| PH23110A (en) | 1989-04-19 |
| EP0127313A1 (en) | 1984-12-05 |
| PT78490B (en) | 1987-02-16 |
| AU2727284A (en) | 1984-11-01 |
| DK207184A (da) | 1984-10-27 |
| HU191749B (en) | 1987-04-28 |
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