125results about "Deoxy/unsaturated sugars" patented technology

The present invention is directed to a method comprising a multistep process for recovering one or more monosaccharides from a solution containing at least two monosaccharides selected from the group consisting of rhamnose, arabinose, xylose and mixtures thereof by using chromatographic separation comprising at least one step, where a weak acid cation exchange resin is used for the chromatographic separation.

A novel method has been found to produce 2,2′-anhydro-1-(β-L-arabinofuranosyl)thymine as a novel useful intermediate compound. A novel method has been further found to produce thymidine from 2,2′-anhydro-1-(β-L-arabinofuranosyl)thymine. A novel method has been further found to L-2′-deoxyribose derivatives as a useful synthetic intermediate through L-2,2′-anhydro-5,6-dihydrocyclouridine derivative. According to these methods, synthesis of various L-nucleic acid derivatives, synthesis of which has been difficult till now.

The invention discloses a method for preparing for 2-deoxyglucose. The method uses D-acetylated dextroglucose and the absolute methanol to obtain the D-gluglucosan on the accelerating effect, and then it dose vacuum distillation to evaporate to dryness the methanol, it adds sulfuric acid water solution on the reacting machine to obtain the 2-deoxyglucose by hydrolyzing, it then uses normal method to do re-crystallization to the course product to obtain the 2-deoxyglucose product.

The invention relates to a method for preparing 1-deoxy-D-xylulose with the combination of a chemical method and an enzymatic method, which comprises the steps as follows: in a water phase system under certain temperature, the glycidol can form glycerol 3-phosphate by inorganic phosphate through ring opening, then the generated L-glycerol 3-phosphate is oxidized by L-GPO to form DHAP under the existence of catalase, the DHAP is converted into DXP under the existence of pyruvic acid, TIM enzyme and DXS, and target molecule DX can be obtained by hydrolyzing the compound through phosphatase. The method organically couples the simple method for preparing the DHAP by taking the stable, cheap and easily available compound as raw material with the method for preparing the DX by using the enzymatic method, the target molecule DX can be obtained through one-step reaction, the yield is high, the purification step is simple and feasible, the DX with high purity (more than 95%) can be obtained, the price of the raw material is low, the nature is stable, and the technical problems of expensive and unstable reaction material, complicated reaction steps, longer time consuming and lower overall yield of the method for preparing DX in the background technology are solved.

The present invention relates to the field of preparing positive electronic radioactive medicine, especially the preparation apparatus and process of 2-fluoro-8 substituent-2-deoxy-beta-D-glucose. The apparatus includes wind bath for heating and cooling the reaction bottle, and negative perssure transmission unit for ultimate product with reduced radioactivity loss, shortened time and raised synthesis efficiency. The technological process combined acid-alkali hydrolysis without possibility of elimination reaction in the 2-position, and it has short hydrolysis period and high radioactive purity and chemical purity of the prepared medicine.

[PROBLEMS] To find out a specific rare sugar having effects of inhibiting the proliferation of vascular endothelial cells and lumen formation and utilize these effects. To provide this rare sugar as a preventive/remedy for diseases with angiogenesis, a cosmetic or a functional food.

[MEANS FOR SOLVING PROBLEMS] A method of controlling the proliferation of vascular endothelial cells characterized by utilizing the vascular endothelial cell proliferation-controlling effect of D-mannose, D-allose, 2-deoxy-D-glucose, 3-deoxy-D-glucose, L-sorbose, 2-deoxy-D-ribose and/or 2-deoxy-L-ribose. A method of inhibiting lumen formation of vascular endothelial cells characterized by utilizing the vascular endothelial cell lumen formation-inhibiting effect of D-allose, D-altrose, D-gulose, D-talose, L-allose, 2-deoxy-D-glucose, 3-deoxy-D-glucose, D-ribose, L-ribose, 2-deoxy-D-ribose and/or 2-deoxy-L-ribose.

A preparation method of a 2-dioxidation-L-ribose relates to a non-natural deoxidation pentose. The invention provides the preparation method that takes D-(-)-ribose (1) as raw material and has simple technology, high optical activity and yield of the 2-dioxidation-L-ribose. (2S, 3R)-2, 3-O- isopropylidene-4-pentenol (2) is prepared through the raw material (1) by a literature method, hydroxide radical of the first carbon in (2) is protected to get (3R, 4S)-3, 4-O-isopropylidene-5- benzyloxy-4-pentene(3), then (3R,4S)-3, 4-O- isopropylidene-5- benzyloxy pentanal (4) is prepared through preferred oxidation at the end of the double linkage (3) in the existence of palladium chloride and cuprous chloride, acetonide protecting group in (4) is removed through catalysis of acid and phenmethyl 2-dioxidation-L-ribose (5) is obtained through cyclization, finally the 2-dioxidation-L-ribose (6) is prepared after the phenmethyl is removed through catalysis.

The present invention provides a one-pot multi-enzyme method for preparing UDP-sugars from simple sugar starting materials. The invention also provides a one-pot multi-enzyme method for preparing oligosaccharides from simple sugar starting materials.

The invention discloses a preparation method of 2-deoxidizing-D-glucose, which is characterized in that in the method, an intermediate 2-deoxidizing-1,3,4,6-tetra-O-acetyl group-D-glucose is prepared by the selective addition reaction of acetyl glucose alkene, and acetyl groups are removed by the acid catalytic hydrolysis reaction of an intermediate 2-deoxidizing-acetyl groups-D-glucose, thus obtaining the 2-deoxidizing-D-glucose after purification. Compared with the prior art, the preparation method has the advantages of simple process, good selectivity, high yield and low cost, thus being a relatively green, environment-protective, economical and efficient synthesis method with broad application prospect.

The invention discloses a preparation method of 2-deoxy-D-glucose, relating to the field of production of active pharmaceutical ingredients. The preparation method comprises the following steps of: a, taking 3, 4, 6-triacetyl glucose alkenes as raw materials, removing acetyl protection groups in the presence of alkalis and then performing benzyl protection to obtain an intermediate I shown as a formula II; b, acid-hydrolyzing the intermediate I obtained in the step a to obtain an intermediate II shown as a formula III; and c, performing hydrogenolysis on the intermediate II obtained in the step b to de-protect and re-crystallizing to obtain the 2-deoxy-D-glucoses shown as a formula I. Compared with the prior art, the preparation method of the 2-deoxy-D-glucoses has the advantages of simple preparation process, easy purification for products, high yield, low cost and the like, and is more beneficial to achieving large-scale industrial production.

The present invention relates to a nutritional composition comprising at least one fucosylated oligosaccharide and at least one N-acetylated oligosaccharide for promoting or inducing a global gut microbiota that is closer to the one of infants fed exclusively with human breast milk, in comparison to infants fed with a conventional nutritional composition. The composition can be an infant formula and is in particular intended for infants between 0 and 12 months of age fed predominantly with infant formula. It promotes a healthy intestinal flora and has beneficial short and long terms effects.

The invention discloses a method of preparing 2-deoxidation-D-glucose. It solves the problems of the complex manufacturing technique and high cost for existing 2-deoxidation-D-glucose. The method includes the following steps: preparing 1.2-deoxidation-2-phenylenemethylamino-D-glucose; preparing 2.2-deoxidation-2- phenylenemethylamino-3,4,5,6-four-O-acetyl-D-glucose; preparing 4.2-deoxidation -2-chorine-3,4,5,6-four-O-acetyl-D-glucose; preparing 5.2-deoxidation-3,4,5,6- four-O-acetyl-D-glucose; preparing 6.2-deoxidation-D-glucose. The raw material of the method is far ranging, and low cost. It has great economic, social, and environment benefit.

The present invention relates to a simple high-effective synthesis method of D-and L-desoxyribose, which includes the following steps: using cheap easily-available D-high-alkyne propanol or L-high-alkyne propanol as raw material, protecting hydroxyl group, using Lindlar catalyst to make selective hydrogenation, using ozone to make oxidation according to different substituent making it react with acid, then react with alkali or react with reducing agent or lewis acid to remove protecting group and making cyclization reaction to obtain the invented product.

This invention relates to 2-deoxygenation-D-glucose preparation method. The method is that D-arabinose is reacted with nitromethane, and the reaction prodect is material, 2 bit acetoxy is selective stripped to get nitryl sugar ene. Borohydride isused to selectively reduce conjugated carbon carbon double bond of the sugar ene to get saturated nitryl sugar. Then the goal compound 2-deoxygenation-D-glucose I sogt after Nef reaction. In this invention, the selectivity is good, yield is improved, the material source is wide, cost is low, and its technique design is reasonable.

The invention belongs to the field of flavonoids compound extraction, and particularly relates to a method for preparing quercetin and rhamnose through rutin. The preparation method comprises the following steps: steaming collected sophora flower buds through steam, air-drying, smashing and seeping the steamed sophora flower buds, removing colloid and chlorophyll impurities through flocculation, performing protection complexing treatment through an antioxidant and a complexing agent, adding a mixed acid to adjust the mixture to be acidic, and heating, pressurizing and hydrolyzing to obtain the quercetin; performing impurity filtration and neutralization on hydrolysis mother liquor subjected to quercetin extraction, degrading glucose through glucose degrading enzyme, and performing decoloring vacuum centrifugal concentration and crystallization after a solution is filtered and separated to obtain a product, namely the rhamnose. Under detection of HPLC (high performance liquid chromatography), the content of the quercetin is over 95 percent; all impurity requirements meet an international standard requirement; in a technical process, rutin hydrolysis mother liquor is also subjected to comprehensive treatment, and rhamnose is obtained through production; the production cost of the production is lowered, and the environmental pollution is alleviated.

The invention discloses a sarcopyramis nepalensis extract. A preparation method of the sarcopyramis nepalensis extract comprises the following steps: taking whole herb of sarcopyramis nepalensis; after crushing the taken whole herb of the sarcopyramis nepalensis, extracting the crushed whole herb of the sarcopyramis nepalensis with ethyl alcohol of 95% for six times, wherein the extraction time each time is one week; performing the filtration, and performing the concentration so as to obtain a medicinal extract. The extract can be used for medicines for nourishing a liver and reducing transaminase, the sarcopyramis nepalensis extract disclosed by the invention can widely affect all the cytokine levels, pharmacological activities of nourishing the liver and reducing the transaminase are realized through regulating the balance of a cytokine network, and scientific basis is provided for the clinical application of the sarcopyramis nepalensis extract.

The invention discloses a method for synthesizing 2-deoxidization-L-ribose, and the method is characterized in that 1-methyl-3, 4-O-isopropyl-2-deoxidization-beta-L-gum sugar reacts in water solution of organic acid with acidity more than that of acetic acid. The final product can be obtained in one step of reaction by the method, and the method has the advantages of simple reaction operation, easy post processing, without the need of column chromatography, high yield and purity, thus being suitable for industrialization production.

The invention discloses a method for preparing 2-deoxy-D-glucose. According to the method, D-glucosamine which is low in price and easy to obtain serves as a starting material, p-anisaldehyde is used for protecting amino, pyridine serves as a solvent under catalysis of 4-dimethylaminopyridine (DMAP), acetic anhydride serves as a reactant for acetylation protection of all hydroxyl groups on D-glucosamine, protecting groups on the amino are removed under the acidic condition to obtain 1,3,4,6-tetra-o-acetyl-2-glucosamine hydrochloride, and the amino is further converted into isothiocyano with PhOC(=S)Cl; AIBN serves as an initiator, a free radical reaction is conducted by means of tris(trimethylsilyl)silane (TTMS-H) and 1,3,4,6-tetra-o-acetyl-2-glucosamine hydrochloride, and finally acetyl is removed to obtain 2-deoxy-D-glucose. According to the novel synthetic route, raw materials are easy to obtain, operation is easy, no chromatographic column separation is involved, the total yield is high, cost is low, and the method is suitable for large-scale production. The preparation method is simple in product aftertreatment, the product is easy to separate, and large-scale production is easy to achieve.