EP1284982A2 - Verfahren zur behandlung von pflanzenmaterial, n-acetylglucosamin-artige verbindungen enthaltende zusammensetzungen sowie verwendung dieser zusammensetzungen - Google Patents

Verfahren zur behandlung von pflanzenmaterial, n-acetylglucosamin-artige verbindungen enthaltende zusammensetzungen sowie verwendung dieser zusammensetzungen

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Publication number
EP1284982A2
EP1284982A2 EP01936594A EP01936594A EP1284982A2 EP 1284982 A2 EP1284982 A2 EP 1284982A2 EP 01936594 A EP01936594 A EP 01936594A EP 01936594 A EP01936594 A EP 01936594A EP 1284982 A2 EP1284982 A2 EP 1284982A2
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EP
European Patent Office
Prior art keywords
linear
alkyl chain
branched
formula
represent
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Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP01936594A
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English (en)
French (fr)
Inventor
Michel Minier
Bruno Kokel
Chadi o Madame KHOURY KHOURY
Christelle Arles
Hélène VERGNEAU
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Universite Pierre et Marie Curie
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Universite Pierre et Marie Curie
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
    • C07H5/04—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to nitrogen
    • C07H5/06—Aminosugars
    • 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
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
    • A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom

Definitions

  • compositions comprising derivatives of the N-acylglucosamine type, use of these compounds as bio-protective agents, and treated plant material, in particular seeds.
  • the subject of the present invention is a process for treating plant material as well as compounds derived from an N-acylglucosamine, compositions comprising derivatives of N-acylglucosamine and their use in particular for phytosanitary purposes.
  • the present invention relates to a process for treating plant seeds, with a view to ensuring their protection against their deterioration during aging, and in particular during their storage.
  • document PCT / FR 96/00200 describes compositions comprising on the one hand a film-forming substance and on the other hand an antioxidant.
  • bioprotective is intended to mean compounds having a beneficial activity for plant material, for example progerminative, antifungal, storage stabilizer, in the case of seeds, or else stimulating the natural defenses of the plant, while being biodegradable.
  • N-acetyl-glucosamine N-acetyl-glucosamine
  • Ri represents R or CO-R where R represents a linear or branched C 5 to C 8 alkyl chain and R 2 represents a linear or branched C 1 to C 4 alkyl chain or an ethynyl group or -NR 3 R where R3 represents CpH 2 p + ⁇ , p ranging from 0 to 4 and R 4 represents C q H 2 q + ⁇ , q ranging from 0 to 4.
  • mineral or organic anion means any anion that is acceptable in such a process and in particular halide (chloride, bromide, iodide), phosphate, sulfate, acetate, carbonate, or benzoate, for example.
  • the alkyl chain (s) is (are) linear (s).
  • R 5 represents a linear or branched C 3 -C 13 alkyl chain.
  • two of A 3 , A 4 and A 6 represent, independently of one another, OC (O) R 5 where R 5 represents a linear or branched C alkyl chain 3 to C 13 , and the third among A 3 , A 4 and A ⁇ represents OH.
  • R5 represents a linear or branched C 3 to C 8 alkyl chain.
  • two among A 3 , A 4 and A ⁇ represent OH and the third among A 3 , A 4 and A ⁇ represents OCOR 5 where R 5 represents a linear or branched C 3 alkyl chain to C 13 . More preferably, in formula I ', R' 2 represents CH 3 .
  • Ri represents COR. More preferably, Ri represents CO-C 7 H ⁇ 5 , COC 5 H t ⁇ , COC9H 19 or COC11H23, and among these, in particular COC H ⁇ 5 or COC 9 H 19 . More preferably, R 2 represents CH 3 . In the previous formulas, the two anomeric forms ⁇ and ⁇ are present. In the aqueous phase, the ⁇ and ⁇ forms can coexist.
  • the present application aims to cover a process for treating vegetable matter.
  • it may be a process for treating seeds intended in particular to prevent their deterioration during aging, in particular during storage.
  • the method may consist in coating or film-coating said seeds, prior to their storage, with a composition incorporating an effective amount of at least one compound of the invention.
  • a composition incorporating an effective amount of at least one compound of the invention There are numerous compositions for coating or coating the seeds in the form of concentrate, dilutable or ready-to-use compositions. These usual generally aqueous compositions are commercially available. Sepiret (designation of compositions sold by SEPPIC), and green clay constitute such usual compositions.
  • the active compounds of the invention are incorporated into these usual compositions.
  • the compositions of the invention may be in the form of an aqueous slurry. However, the compounds of the invention were applied in aqueous or hydroalcoholic solution.
  • plant material is meant not only seeds, seeds but also standing plants, roots, tubers, onions, and plant cell cultures.
  • seeds or seeds are treated.
  • the aforementioned coating or lamination of the seeds is carried out either by spray-drying, or by churning.
  • Spray-drying is a known process for coating solid forms dry.
  • the churning technique is a process also known for the film-coating or coating of solid forms by the wet method and consists here of agitating the seeds inside a rotary mixer in the presence of a film-forming composition as described above.
  • Other modes of application than the coating methods provided above can be implemented, in particular on plant material other than seeds, and for example spraying, soil treatment, spreading and watering .
  • the compounds of the invention are incorporated in the usual compositions for spray treatment, soil treatment, spreading, or watering.
  • the application is carried out at a rate of 0.1 mg to 100 mg of compound of formula I or I 'per gram of seed, preferably 1 mg to 5 mg.
  • this can comprise 1 to 40, preferably 5 to 20 mg of compound of formula l / g of aqueous slurry, or 1 to 40, of preferably 3.5 to 15% of at least one compound of formula I or I 'in the slurry by weight of dry extract.
  • the present invention also relates to compositions, for phytosanitary use in particular, comprising at least one compound of the invention as active agent.
  • the present invention relates to compositions comprising at least one compound of formula I or I 'above and a support acceptable for its phytosanitary use.
  • the compound of formula I or I ′ is present in proportions ranging from 1 to 97% of compound, by weight of dry extract in the composition.
  • the present invention relates to the compounds of formula I with the exception of those for which R 1 represents CO (CH 2 ) 6 CH 3 or CO (CH 2 ) 14 CH 3 and R 2 is CH 3 , and the compounds of formula I 'with the exception of those for which A 6 , A 4 and A 3 represent OH, compounds where R ' 2 represents CH3, A 3 and A4 represent OH and A 6 represents OC (O) (CH 2 ) 6 CH3 or OC (O) (CH 2 ) ⁇ 4 CH 3 , and compounds where R ' 2 represents CH 3 , A 4 and A 6 represent OH and A 3 represents OC (O) (CH 2 ) 6 CH 3 or OC (O) (CH 2 ) ⁇ oCH 3 or OC (O) (CH 2 ) 14 CH 3 .
  • the compounds of formula I of the invention can be prepared according to the following general scheme: Reaction: monoesterification on C6 of the NAG motif
  • R 2 is CH 3 and R is COC n - ⁇ H 2n + ⁇ whose implementation is within the reach of those skilled in the art, as well as the variants making it possible to obtain the other derivatives of the NAG referred to by the formula I.
  • Pi is a protective group, for example the benzyl group.
  • the carbon C1 can be protected by an appropriate group (for example benzyl for the ester), we proceed to esterification with the corresponding reagent (acid chloride) and then deprotects.
  • an appropriate protecting group for example benzyl for the ester
  • a suitable protecting group is allyl.
  • the procedure is the same with a larger amount of the reagent. To triester it, with excess reagent.
  • the method described by Femandez-Bolanos et al., Anales de Quimica (1982) 423 can be used.
  • the corresponding reagents are acid chloride to prepare esters, halides, for example alkyl bromide to prepare ethers, corresponding alkylsulfonyl chlorides (R5 SO 2 Cl) to prepare the compounds where A 3 , A 4 or A 6 represent OSO 2 R 5 .
  • the compounds of the invention incorporated into a film-coating composition, can provide both antifungal protection and promotion of germination, significantly.
  • compositions of the invention can comprise at least one film-forming agent.
  • a film-forming substance suitable in the context of the present invention generally consists of a polymer allowing the formation of a film permeable to water and gas exchanges, biodegradable and without phytotoxic effect for plant material.
  • cellulose derivatives in particular cellulose esters or ethers such as, for example, methylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, cellulose acetophthalate, acetate of cellulose or ethylcellulose; natural polysaccharides such as in particular modified starches, gums such as guar gum, xanthan gum or gum arabic, alginates, chitosans; as well as vinyl or acrylic derivatives.
  • antioxidant agent capable of being used in the context of the present invention, mention will be made more especially of ascorbic acid and its salts (in particular calcium and sodium); tocopherols, especially vitamin E; polyamines, such as, for example, spermine, spermidine, putrescine, agmatine, cadaverine; flavonoids such as, for example, quercetin, myricetin, kaempferol, catechin, luteolin; carotenoids, in particular ⁇ -carotene; phenolic compounds such as, for example, thymol, carvacrol, zingerone, 6-gingerol, hydroxytyrosol, butylhydroxyanisole, butylhydroxytoluene; amino acids such as arginine, histidine, cysteine, tryptophan, lysine, threonine and magnesium methioninate; squalene or monoterpenes such as, for example,
  • compositions of the invention are aqueous and therefore, preferably, active agents will be chosen, in particular water-soluble film-forming polymers, in particular from those mentioned above.
  • compositions according to the invention can also comprise at least one plasticizing substance, in an amount by weight, expressed relative to the dry matter of the composition, of between 0% and 50%, preferably between 5% and 30 %.
  • plasticizing substances make it possible to improve the spreading qualities of the main film, as well as its physical properties.
  • plasticizing substances which may be used for this purpose, mention will be made more particularly of glycerol, sorbitol, glycols, and their aliphatic ethers or esters; preferably nonionic surfactants in the form of carbohydrate or glycerol esters or ethers or also more or less ethoxylated alcohols and fatty acids.
  • the compounds of the invention can have surfactant properties, in particular as nonionic surfactants, the incorporation of these compounds in the compositions of the invention can make it possible to reduce the level of usual surfactant.
  • the compounds of the invention are biodegradable, this reduction has a certain advantage from the point of view of the biodegradability of the compositions applied.
  • the compositions according to the invention may also comprise one or more additives chosen from dyes and fillers usually used to modify the properties of the coating material and the protection of said material, in an amount by weight, expressed relative to the dry matter of the composition, between 0% and 90%, preferably between 5% and 70%.
  • dyes which may be used for this purpose, the following dyes may be mentioned, for example, in soluble or in the form of lacquers: methyl violet 2B, cochineal red, orange yellow S, as well as pigments such as mica-titanium, titanium dioxide, iron oxide, zinc oxide, l magnesium oxide, black 7 or else pigment pastes containing for example red 48, red 1 12, blue 15, green 7 dispersed in a suitable solvent.
  • opacifying agents such as, for example, talc, mica, cellulose
  • water repellents such as fatty acids and their derivatives, silicone polymers and wetting agents promoting the spreading of the film-forming composition, and therefore making it possible to improve the coverage and the appearance of the coated seeds.
  • a phytosanitary composition according to the invention can be either in liquid form with a dry matter content of between 10% and 70%, preferably between 20 and 40%, or also in dry form, that is to say in form of powders or granules, preferably water-dispersible.
  • Such a composition can be prepared by known methods widely described in the literature to which a person skilled in the art may refer, and in particular to patents FR-A2,548,675 and US-4,665,648.
  • different active materials such as in particular fungicides, insecticides, herbicides, molluscids, repellents or growth substances, may be added to the phytosanitary compositions according to the invention.
  • compositions of the invention may be added in an amount by weight, expressed relative to the dry matter of the composition, of between 1% and 50%, preferably between 3% and 30%.
  • these therefore consist of a coating or film-coating composition in which at least one compound of formula I or i 'is incorporated.
  • the composition of the invention is used for the above-mentioned film-coating treatment in an amount by weight of between 2 and 50 expressed in grams of dry matter per kilogram of seed.
  • the amount of composition used can be between 100 and 1000 grams of dry matter per kilogram of seed.
  • the present application aims to cover the seeds treated with the phytosanitary compositions described above in particular by means of the above methods.
  • the deuterated solvent is DMSO.
  • the chemical shifts are expressed in ppm.
  • Example 1 2-acetamido-2-deoxy- (6) O-stearoyl D-glucopyranose (C18-NAG).
  • C18-NAG O-stearoyl D-glucopyranose
  • Ci 8 2-acetamido-2-deoxy- (6) O-stearoyl D-glucopyranose.
  • the yield obtained is of the order of 35 to 40%.
  • the solvent used is deuterated DMSO.
  • ⁇ (ppm) 0.85 (t; 3H; CH 3 10 "), 1.24 (s; 12H; CH 2 from 9" to 4 "), 1.51 (m; 2H; CH 2 3") , 1.82 (s; 3H; CH 3 2 '), 2.28 (t; 2H; CH 2 2 "), 3.05 to 4.31 (several m; 6H; 4 CH cycle; CH 2 6) , 4.76 (d; 1 H; OH), 4.89 (m; 1 H; CH cycle), 5.19 (d; 1 H; OH), 6.57 (d; 1 H; OH), 7, 69 (d; 1 H; NH) 2. 13 C NMR spectrum
  • the solvent used is deuterated DMSO.
  • ⁇ (ppm) 14.21 (CH 3 10 "), 22.35 (CH 2 9"), 22.91 (CH 3 2 '), 24.73 (CH 2 8 "), 28.71 to 29 , 12 (CH 2 7 “to 5"), 31, 53 (CH 2 4 "), 33.70 (CH 2 3"), 36.14 (CH 2 2 "), 54.38 (CH 2), 64.02 to 70.52 (CH 4, 5, 6), 71, 38 (CHOH 3), 90.94 (CHOH 1), 169.60 (CHO 1 '), 173.19 (CHO 1 ").
  • Example 3 The addition of lauroyl chloride (2.47 g) to the NAG flask (2.5 g) and pyridine (0.88 g) in DMF (30 ml) was carried out as for Example 3. The solution obtained was left for fifteen hours at room temperature, still with stirring and under argon. The solution, which had become clear, was then hydrolyzed with 5 ml of water and the solvent was evaporated. 30 mL of water was added to the yellow-orange gum. After a waiting time of approximately 1 h, gelling was observed: the particles are such that two different procedures for washing with water can be chosen. The whole was filtered on frit No. 3, or treated by the method by successive centrifugations as in Example 3.
  • the solvent used is deuterated DMSO.
  • ⁇ (ppm) 0.85 (t; 3H; CH 3 14 "), 1.24 (s; 20H; CH 2 from 13" to 4 "), 1.51 (m; 2H; CH 2 3") , 1.82 (s; 3H; CH 3 2 '), 2.28 (t; 2H; CH 2 2 "), 3.09 to 4.31 (several m; 6H; 4 CH cycle; CH 2 6), 4.76 (d; 1 H; OH), 4.90 (m; 1 H; CH cycle), 5.19 (d; 1 H; OH), 6.57 (d; 1 H ; OH), 7.69 (d; 1H; NH).
  • the solvent used is deuterated DMSO.
  • ⁇ (ppm) 0.86 (t; 3H; CH 3 6 "), 1.26 (s; 4H; CH 2 5" and 4 "), 1.52 (m; 2H; CH 2 3"), 1.82 (s; 3H; CH 3 2 '), 2.25 (t; 2H; CH 2 2 "), 3.13 to 4.32 (several m; 6H; 4CH cycle; CH 2 6), 4 , 75 (d; 1 H; OH), 4.89 (m; 1 H; CH cycle), 5.19 (d; 1 H; OH), 6.57 (d; 1 H; OH), 7, 69 (d; 1H; NH).
  • the organic phase was then washed with 20 ml of a saturated solution of sodium hydrogen carbonate in order to pass the hexanoic acid into the aqueous phase in the form of sodium hexanoate.
  • the organic phase was dried over MgSO 4 and then evaporated.
  • the residual brown oil was triturated in pentane several times until a fine powder was obtained.
  • the powder was isolated by decantation, dried under vacuum and then dissolved in 100 ml of ether.
  • the starting material and part of the monomer have not been soluble in ether and formed a white solid which was collected by vacuum filtration and dried.
  • the ethereal phase was evaporated.
  • the solid obtained was recrystallized from an ether / pentane mixture to obtain a 90% pure product with a yield of approximately 25%. This product was then debenzylated by hydrogenation at atmospheric pressure with a palladium on carbon catalyst.
  • the solvent used is deuterated DMSO.
  • ⁇ (ppm) 0.86 (t; 3H; CH 3 4 "), 1.52 (q; 2H; CH 2 3"), 1.82 (s; 3H; CH 3 2 '), 2.25 (t; 2H; CH 2 2 "), 3.13 to 4.42 (several m; 6H; 4CH cycle.
  • CH 2 6 4.75 (d; 1 H; OH), 4.89 (m; 1 H; CH cycle), 5.19 (d; 1 H; OH), 6.57 (d; 1 H; OH), 7.69 (d; 1 H; NH).
  • NAG N-acetylglucosamine
  • the agar medium consisted of: in g / l of demineralized water: Yeast extract 2, KH2PO4: 1.5; K2HPO4: 1.5; Mg (S ⁇ 4) .7H2 ⁇ : 0.3; NaN ⁇ 3: 3 and agar: 14. Incubation temperature: 16 ° C.
  • the antifungal effect was measured by the inhibition of the growth of the hyphae of fungi, after 7 days of incubation, by comparison with the results obtained with film-forming preparations not containing the additives (reference preparations).
  • Contaminated seed is a seed that has given rise to the development of hyphae of the fungus.
  • Dg number of sprouted seeds (test) - number of sprouted seeds (reference)
  • TEA (% contaminated seeds reference -% contaminated seeds IOO test (% contaminated seeds reference) and the TEG germination efficiency rate by:
  • TEG (% germinated seeds test -% germinated seeds reference xlOO (% germinated seeds reference)
  • the table shows a significant antifungal efficacy on the part of C8-NAG at the three concentrations tested: 5, 10 and 50 mg / g as well as for Hecameg (5 mg / g). However, there is an increase significant germination for an average concentration of C8-NAG (10 mg / g) while Hecameg reduces it.
  • Example B Coating with C12-NAG alone in solution or in hydroalcoholic suspension.
  • Film-coating tests were carried out by stirring, for approximately one minute, wheat seeds in suspensions or hydroalcoholic solutions of C12-NAG. These suspensions or solutions were produced by mixing 150 mg of C12-NAG with 4 ml of hydroalcoholic solvent.
  • the solvents tested were pure water, an aqueous ethanol solution at 50% volume / volume and an aqueous ethanol solution at 95% (v / v).
  • Control manipulations with other batches of seeds, consisted in carrying out the protocol described above using hydroalcoholic solutions of the same titles, without active compound, in order to control the effect of the simple impregnation of the seeds by the diluents .
  • the control batches and the batches comprising C12-NAG were dried simultaneously under the same current of hot air. Drying was stopped when the control batch regained its initial weight before impregnation.
  • the film-coating agent is Sepiret Argent 7017 ® .
  • 5 and 6 g of this film-coating suspension are respectively required to film 110 seeds.
  • Pea seeds contaminated with Botrytis sp. and Ascochyta pinodes were coated with Sepiret Argent 7017® (reference) and with NAG and C8-NAG introduced into the coatings, under the same conditions as above.
  • the agar is composed of glucose (10 g / l) and Agar-Agar (12.5 g / l). After addition of the Cn-NAG solutions, the agar is poured into sterile Petri dishes. The dishes are then seeded with 0.3 ml of mushroom spore suspensions containing between 2.10 5 and 4.10 5 spores / ml. After incubation for approximately 20 hours at 19 ° C. in the dark, the germination of the spores and the length of the hyphae developed by the fungi are evaluated by observation under a microscope.
  • the following table shows the results obtained with the Botrytis cinerea (strains A and B) and Fusarium roseum v. graminearum.

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental Sciences (AREA)
  • Biotechnology (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Plant Pathology (AREA)
  • Pest Control & Pesticides (AREA)
  • Biochemistry (AREA)
  • Dentistry (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Agronomy & Crop Science (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Cultivation Of Plants (AREA)
EP01936594A 2000-05-19 2001-05-18 Verfahren zur behandlung von pflanzenmaterial, n-acetylglucosamin-artige verbindungen enthaltende zusammensetzungen sowie verwendung dieser zusammensetzungen Withdrawn EP1284982A2 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0006477 2000-05-19
FR0006477A FR2809104B1 (fr) 2000-05-19 2000-05-19 Procede de traitement de matiere vegetale, compositions comportant des derives du type n-acylglucosamine, utilisation de ces composes en tant qu'agents bio- protecteurs, et matiere vegetale traitee.
PCT/FR2001/001549 WO2001087902A2 (fr) 2000-05-19 2001-05-18 Procede de traitement de matiere vegetale compositions comportant des derives du type n-acylglucosamine utilisation de ces composes

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Publication Number Publication Date
EP1284982A2 true EP1284982A2 (de) 2003-02-26

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EP01936594A Withdrawn EP1284982A2 (de) 2000-05-19 2001-05-18 Verfahren zur behandlung von pflanzenmaterial, n-acetylglucosamin-artige verbindungen enthaltende zusammensetzungen sowie verwendung dieser zusammensetzungen

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EP (1) EP1284982A2 (de)
JP (1) JP2004522693A (de)
AU (1) AU2001262470A1 (de)
CA (1) CA2409135A1 (de)
FR (1) FR2809104B1 (de)
WO (1) WO2001087902A2 (de)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9315532B2 (en) * 2005-05-24 2016-04-19 The Johns Hopkins University Fatty acid carbohydrate hybrid molecules as therapeutic agents and methods thereof
WO2014070606A1 (en) * 2012-10-29 2014-05-08 Pioneer Hi-Bred International, Inc. Use of glucosamine amides as plant growth and yield enhancers
WO2015130893A1 (en) * 2014-02-28 2015-09-03 E. I. Du Pont De Nemours And Company Synthetic oligoglucosamines for improvement of plant growth and yield

Family Cites Families (6)

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Publication number Priority date Publication date Assignee Title
JPS5562004A (en) * 1978-11-02 1980-05-10 Kureha Chem Ind Co Ltd Control agent against plant viral disease
DE3308806A1 (de) * 1983-03-12 1984-09-13 Basf Ag, 6700 Ludwigshafen Fungizide mittel, substituierte glucopyranosylamine und verfahren zur bekaempfung von pilzen
FR2548675B1 (fr) * 1983-07-06 1987-01-09 Seppic Sa Compositions filmogenes pour enrobage des formes solides de produits pharmaceutiques ou alimentaires et produits obtenus revetus desdites compositions
EP0352230A3 (de) * 1988-07-22 1991-04-10 Ciba-Geigy Ag Optische Isomere eines Palmitoylglucopyranosids, ein Verfahren zu deren Herstellung und deren Verwendung
ATE211468T1 (de) * 1996-07-22 2002-01-15 Sankyo Co Neuraminsäuredervate, ihre herstellung und medizinische verwendung
FR2785149B1 (fr) * 1998-10-28 2001-12-28 Univ Paris Curie Composition fongicide a base d'enzymes

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0187902A3 *

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Publication number Publication date
FR2809104B1 (fr) 2002-08-02
JP2004522693A (ja) 2004-07-29
CA2409135A1 (fr) 2001-11-22
AU2001262470A1 (en) 2001-11-26
WO2001087902A2 (fr) 2001-11-22
WO2001087902A3 (fr) 2003-01-09
FR2809104A1 (fr) 2001-11-23

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