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 disse

Info

Publication number: NO841567L
Authority: NO; Norway
Prior art keywords: alkyl; group; oxo; dihydro; hydrogen atom
Prior art date: 1983-04-26

Application number

NO841567A

Other languages

English (en)

Norwegian (no)

Inventor

Samuel Eugene Sherba

Harlow Lester Warner

Original Assignee

Rohm & Haas

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-04-26

Filing date

1984-04-18

Publication date

1984-10-29

1984-04-18 Application filed by Rohm & Haas filed Critical Rohm & Haas

1984-10-29 Publication of NO841567L publication Critical patent/NO841567L/no

Links

238000000034 method Methods 0.000 title claims description 50
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
244000098338 Triticum aestivum Species 0.000 claims description 19
239000011734 sodium Substances 0.000 claims description 19
229910052708 sodium Inorganic materials 0.000 claims description 18
235000021307 Triticum Nutrition 0.000 claims description 14
125000003545 alkoxy group Chemical group 0.000 claims description 14
229910052799 carbon Inorganic materials 0.000 claims description 12
238000011161 development Methods 0.000 claims description 12
230000018109 developmental process Effects 0.000 claims description 12
210000001161 mammalian embryo Anatomy 0.000 claims description 12
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
230000012010 growth Effects 0.000 claims description 11
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
241000218922 Magnoliophyta Species 0.000 claims description 10
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 10
238000004519 manufacturing process Methods 0.000 claims description 10
239000000126 substance Substances 0.000 claims description 10
125000003342 alkenyl group Chemical group 0.000 claims description 9
229910052736 halogen Inorganic materials 0.000 claims description 9
125000004430 oxygen atom Chemical group O* 0.000 claims description 9
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 8
125000003118 aryl group Chemical group 0.000 claims description 8
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
230000021121 meiosis Effects 0.000 claims description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 8
229910052717 sulfur Inorganic materials 0.000 claims description 8
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 7
125000004414 alkyl thio group Chemical group 0.000 claims description 7
229910052794 bromium Inorganic materials 0.000 claims description 7
235000013339 cereals Nutrition 0.000 claims description 7
229910052801 chlorine Inorganic materials 0.000 claims description 7
239000000460 chlorine Chemical group 0.000 claims description 7
125000004093 cyano group Chemical group *C#N 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 7
229910052760 oxygen Inorganic materials 0.000 claims description 7
239000001301 oxygen Substances 0.000 claims description 7
239000011591 potassium Chemical group 0.000 claims description 7
229910052700 potassium Inorganic materials 0.000 claims description 7
125000000446 sulfanediyl group Chemical group *S* 0.000 claims description 7
125000004953 trihalomethyl group Chemical group 0.000 claims description 7
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical group ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 6
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 6
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
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 5
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
229910052731 fluorine Inorganic materials 0.000 claims description 5
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 4
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 4
JDEKUYKSOCTBJT-UHFFFAOYSA-N 1-(4-chlorophenyl)-6-methyl-4-oxopyridazine-3-carboxylic acid Chemical compound CC1=CC(=O)C(C(O)=O)=NN1C1=CC=C(Cl)C=C1 JDEKUYKSOCTBJT-UHFFFAOYSA-N 0.000 claims description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
229910052783 alkali metal Inorganic materials 0.000 claims description 4
125000005189 alkyl hydroxy group Chemical group 0.000 claims description 4
125000003710 aryl alkyl group Chemical group 0.000 claims description 4
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
239000011737 fluorine Chemical group 0.000 claims description 4
229910052740 iodine Chemical group 0.000 claims description 4
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
150000002814 niacins Chemical class 0.000 claims description 4
235000001968 nicotinic acid Nutrition 0.000 claims description 4
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
235000007319 Avena orientalis Nutrition 0.000 claims description 3
244000075850 Avena orientalis Species 0.000 claims description 3
240000005979 Hordeum vulgare Species 0.000 claims description 3
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235000007164 Oryza sativa Nutrition 0.000 claims description 3
NPYPAHLBTDXSSS-UHFFFAOYSA-N Potassium ion Chemical compound [K+] NPYPAHLBTDXSSS-UHFFFAOYSA-N 0.000 claims description 3
241000209056 Secale Species 0.000 claims description 3
235000007238 Secale cereale Nutrition 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
240000008042 Zea mays Species 0.000 claims description 3
235000002017 Zea mays subsp mays Nutrition 0.000 claims description 3
150000001340 alkali metals Chemical class 0.000 claims description 3
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
FAMKRFUSYRJPHL-UHFFFAOYSA-N ethyl 2-(4-bromophenyl)-3-ethyl-5-oxopyridazine-4-carboxylate Chemical compound N1=CC(=O)C(C(=O)OCC)=C(CC)N1C1=CC=C(Br)C=C1 FAMKRFUSYRJPHL-UHFFFAOYSA-N 0.000 claims description 3
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
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
235000009566 rice Nutrition 0.000 claims description 3
125000006536 (C1-C2)alkoxy group Chemical group 0.000 claims description 2
OIIRJRBCKCBJEO-UHFFFAOYSA-N 2-(3-ethyl-5-oxo-2-phenylpyridazin-4-yl)acetic acid Chemical compound CCC1=C(CC(O)=O)C(=O)C=NN1C1=CC=CC=C1 OIIRJRBCKCBJEO-UHFFFAOYSA-N 0.000 claims description 2
LWTAPBNBGCXWOR-UHFFFAOYSA-N 2-[2-(3,4-dichlorophenyl)-3-methyl-5-oxopyridazin-4-yl]acetic acid Chemical compound CC1=C(CC(O)=O)C(=O)C=NN1C1=CC=C(Cl)C(Cl)=C1 LWTAPBNBGCXWOR-UHFFFAOYSA-N 0.000 claims description 2
240000006394 Sorghum bicolor Species 0.000 claims description 2
235000011684 Sorghum saccharatum Nutrition 0.000 claims description 2
244000062793 Sorghum vulgare Species 0.000 claims description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 2
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 2
125000004104 aryloxy group Chemical group 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
125000001841 imino group Chemical group [H]N=* 0.000 claims description 2
GQFJDWYHPRLNHR-UHFFFAOYSA-N karetazan Chemical compound CCN1C(C)=CC(=O)C(C(O)=O)=C1C1=CC=C(Cl)C=C1 GQFJDWYHPRLNHR-UHFFFAOYSA-N 0.000 claims description 2
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235000019713 millet Nutrition 0.000 claims description 2
239000011593 sulfur Substances 0.000 claims description 2
150000004892 pyridazines Chemical class 0.000 claims 2
WSZOBWHBSHCAMH-UHFFFAOYSA-N 1-(4-chlorophenyl)-6-methyl-4-oxo-5-propanoylpyridazine-3-carboxylic acid Chemical compound N1=C(C(O)=O)C(=O)C(C(=O)CC)=C(C)N1C1=CC=C(Cl)C=C1 WSZOBWHBSHCAMH-UHFFFAOYSA-N 0.000 claims 1
235000019714 Triticale Nutrition 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
230000004883 flower formation Effects 0.000 claims 1
125000004001 thioalkyl group Chemical group 0.000 claims 1
241000228158 x Triticosecale Species 0.000 claims 1
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 42
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 29
238000006243 chemical reaction Methods 0.000 description 22
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239000002253 acid Substances 0.000 description 15
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210000002257 embryonic structure Anatomy 0.000 description 12
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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)
Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
Plural Heterocyclic Compounds (AREA)
Pretreatment Of Seeds And Plants (AREA)

NO841567A 1983-04-26 1984-04-18 Fremgangsmaate til fremstilling av haploide froe og dupolider og homozygote planteslekter av disse NO841567L (no)

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 (fr)
AU (1)	AU562972B2 (fr)
BR (1)	BR8401899A (fr)
CA (1)	CA1236700A (fr)
DE (1)	DE3478985D1 (fr)
DK (1)	DK207184A (fr)
ES (1)	ES8605139A1 (fr)
GR (1)	GR79912B (fr)
HU (1)	HU191749B (fr)
IL (1)	IL71635A (fr)
NO (1)	NO841567L (fr)
NZ (1)	NZ207927A (fr)
PH (1)	PH23110A (fr)
PT (1)	PT78490B (fr)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
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
US7502113B2 (en)	2004-08-26	2009-03-10	Monsanto Technology Llc	Automated seed sampler and methods of sampling, testing and bulking seeds
US7703238B2 (en)	2004-08-26	2010-04-27	Monsanto Technology Llc	Methods of seed breeding using high throughput nondestructive seed sampling
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
EP2595465B1 (fr)	2010-07-20	2021-06-02	Monsanto Technology LLC	Systèmes automatisés pour le retrait d'échantillons tissulaires de semences, et procédés associés
US9677082B2 (en)	2013-03-15	2017-06-13	Syngenta Participations Ag	Haploid induction compositions and methods for use therefor
UA125929C2 (uk) *	2015-11-18	2022-07-13	Сінгента Партісіпейшнс Аг	Спосіб індукування утворення гаплоїдних зародків при схрещуванні між двома рослинами
US20200221654A9 (en) *	2016-05-03	2020-07-16	Bayer Cropscience Aktiengesellschaft	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
IL312720A (en)	2021-12-17	2024-07-01	Syngenta Crop Protection Ag	Herbicidal pyridone derivatives
JP2025513597A (ja)	2022-04-27	2025-04-24	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２－オキソ－ニコチン酸誘導体
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
AU2023280572A1 (en)	2022-06-01	2024-12-05	Syngenta Crop Protection Ag	Herbicidal derivatives
CA3255970A1 (fr)	2022-06-01	2023-12-07	Syngenta Crop Protection Ag	Dérivés herbicides
AR130324A1 (es)	2022-09-01	2024-11-27	Syngenta Crop Protection Ag	Derivados herbicidas
JP2025541749A (ja)	2022-12-01	2025-12-23	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
PY2430925A (es)	2023-04-27	2025-01-23	Syngenta Crop Prot Ag	Derivados herbicidas
WO2025087845A1 (fr)	2023-10-23	2025-05-01	Syngenta Crop Protection Ag	Dérivés herbicides
WO2025108824A1 (fr)	2023-11-21	2025-05-30	Syngenta Crop Protection Ag	Dérivés herbicides
WO2025119663A1 (fr)	2023-12-05	2025-06-12	Syngenta Crop Protection Ag	Dérivés herbicides
WO2026002882A1 (fr)	2024-06-27	2026-01-02	Syngenta Crop Protection Ag	Dérivés herbicides
WO2026008582A1 (fr)	2024-07-04	2026-01-08	Syngenta Crop Protection Ag	Dérivés d'acide 5-oxo-pyridazine-4-carboxylique en tant qu'herbicides

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* Cited by examiner, † Cited by third party
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
EP0037134A1 (fr) *	1980-03-26	1981-10-07	Shell Internationale Researchmaatschappij B.V.	Dérivés de pyridazine, procédé pour leur préparation, compositions les contenant, leur utilisation dans des méthodes de régulation de croissance des plantes, d'augmentation du rendement des plants de fève de soja, de stérilisation des anthères mâles des plants incluant les plants de céréales à petits grains, de même que dans une méthode de production de semence F1 hybride
EP0037133A1 (fr) *	1980-03-26	1981-10-07	Shell Internationale Researchmaatschappij B.V.	Dérivés de pyridazinone, procédé pour leur préparation, compositions les contenant, leur utilisation dans une méthode de régulation de croissance des plantes, d'augmentation du rendement des plants de fèves de soja, de stérilisation des anthères mâles des plants incluant les plants de céréales à petits grains, de même que dans une méthode de production de semence F1 hybride
AU539399B2 (en) *	1980-05-12	1984-09-27	Zeneca Limited	Substituted oxonicotinates

1984
- 1984-04-12 CA CA000451846A patent/CA1236700A/fr not_active Expired
- 1984-04-18 PH PH30579A patent/PH23110A/en unknown
- 1984-04-18 NO NO841567A patent/NO841567L/no unknown
- 1984-04-19 NZ NZ207927A patent/NZ207927A/en unknown
- 1984-04-24 GR GR74481A patent/GR79912B/el unknown
- 1984-04-24 ES ES531843A patent/ES8605139A1/es not_active Expired
- 1984-04-24 BR BR8401899A patent/BR8401899A/pt not_active Application Discontinuation
- 1984-04-25 IL IL71635A patent/IL71635A/xx unknown
- 1984-04-25 EP EP84302772A patent/EP0127313B1/fr not_active Expired
- 1984-04-25 DK DK207184A patent/DK207184A/da not_active Application Discontinuation
- 1984-04-25 DE DE8484302772T patent/DE3478985D1/de not_active Expired
- 1984-04-25 HU HU841595A patent/HU191749B/hu not_active IP Right Cessation
- 1984-04-26 PT PT78490A patent/PT78490B/pt not_active IP Right Cessation
- 1984-04-26 AU AU27272/84A patent/AU562972B2/en not_active Ceased

Also Published As

Publication number	Publication date
DK207184D0 (da)	1984-04-25
DE3478985D1 (en)	1989-08-24
CA1236700A (fr)	1988-05-17
HUT39061A (en)	1986-08-28
PT78490A (en)	1984-05-01
ES531843A0 (es)	1986-03-16
BR8401899A (pt)	1984-12-04
PH23110A (en)	1989-04-19
HU191749B (en)	1987-04-28
NZ207927A (en)	1987-09-30
EP0127313B1 (fr)	1989-07-19
GR79912B (fr)	1984-10-31
AU562972B2 (en)	1987-06-25
AU2727284A (en)	1984-11-01
PT78490B (en)	1987-02-16
DK207184A (da)	1984-10-27
IL71635A (en)	1988-12-30
ES8605139A1 (es)	1986-03-16
EP0127313A1 (fr)	1984-12-05

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