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Matches 301 - 350 out of 386

Document Document Title
JPH10502824A
PCT No. PCT/EP95/02883 Sec. 371 Date Jan. 8, 1997 Sec. 102(e) Date Jan. 8, 1997 PCT Filed Jul. 19, 1995 PCT Pub. No. WO96/03518 PCT Pub. Date Feb. 8, 1996The invention concerns a process for preparing mercapto compounds comprising the st...  
JPH1036859A
To achieve effective desulfurization by decomposing organic sulfur compounds by using a microorganism belonging to Paenibacillus genus and having ability to decompose organic sulfur compounds. A culture medium for a high temperature-desu...  
JPH09322787A
To inexpensively produce the subject compound useful as a synthetic intermediate, etc., of a carbapenem compound having antibacterial activity by acting a hydrolase derived from an animal organ or a microorganism to a glutaric acid diest...  
JPH09187288A
To obtain a natural flavor-imparted thiol via a biological conversion in high efficiency by bringing a specific cysteine S-complex into contact with a microorganism having a β-C-S-lyase type enzyme activity and usable in foods. A specif...  
JP2612671B2
PURPOSE: To efficiently prepare the subject compound useful as a synthetic intermediate or the like for a calcium channel inhibitor diltiazem in good yield by acylating a racemic compound of a specific phenylpropionic acid derivative wit...  
JPH09107984A
To obtain the subject polymer excellent in mechanical strength, thermal properties, electrical properties and hot water resistance, thus useful for e.g. engineering plastics, by reaction of a phenol derivative in the presence of an enzym...  
JPH0984591A
To produce a new carotenoid sulfate, soluble in a water-soluble solvent and useful as a color tone improving agent and a redyeing agent for cultured fishes and shellfishes, a food additive, etc., by culturing a microorganism of the genus...  
JPH08510121A
PCT No. PCT/EP94/01640 Sec. 371 Date Nov. 14, 1995 Sec. 102(e) Date Nov. 14, 1995 PCT Filed May 16, 1994 PCT Pub. No. WO94/26918 PCT Pub. Date Nov. 24, 1994Process for preparing S-methylmercapto and mercapto compounds comprising the step...  
JP2516777B2  
JPH0898696A
PURPOSE: To reduce a compound without by-products at ordinary temperature and normal pressure by reacting a carboxylic acid, a CO compound, an SO compound, etc., with a reductase-containing resting microorganism in a biphase medium compo...  
JPH0829095B2
A DNA fragment that codes for the portion of Bacillus thuringiensis crystal protein peptide that is toxic to lepidopteran insects. The invention also comprises the DNA and amino acid sequences for the disclosed toxin-encoding DNA fragmen...  
JPH0797970B2
A process for the preparation of 2-hydroxy-4-methylthiobutyric acid having improved color, odor and lower viscosity. 2-hydroxy-4-methylthiobutyronitrile is hydrolyzed with sulfuric acid having an initial strength of between about 50% by ...  
JPH0722512B2  
JPH0667895B2  
JPH06504761A
(57) [Summary] Since this publication is application data before electronic filing, summary data is not recorded.  
JPH06504447A
(57) [Summary] Since this publication is application data before electronic filing, summary data is not recorded.  
JPH0634753B2  
JPH0634729B2
PURPOSE:To obtain the titled polymer capable of accepting an asymmetric factor in the polymer main chain and of containing various functional groups and useful as a water- and oil-repellent fiber, an asymmetry-inducing catalyst, etc., by...  
JPH0632633B2  
JPH0654695A
PURPOSE: To selectively cleave organic C-S bonds by a microorganism-based biochemical reagent. CONSTITUTION: This invention relates to a microbial process for selective cleavage of organic C-S bonds by contacting sulfur-contg. organic ca...  
JPH0614785A
PURPOSE: To obtain a mixture of an enatiomerically enriched unreacted 1,2-diol monosulfonate with a corresponding antipodal enantiomerically enriched ester. CONSTITUTION: This method for enzymatically esterifying a 1,2-diol monosulfonate...  
JPH0571236B2  
JPH0569518B2
Process for preparing optically active 2-aryloxy- or 2-arylthioalkanoic acids by enantioselective hydrolysis of the corresponding racemic amides in the presence of a microorganism or of an enzyme selected as a function of its ability to ...  
JPH05229964A
PURPOSE: To provide a simple and easy method to produce a sulfide and amino acid or its deriv. labeled with 35S when these compds. are required. CONSTITUTION: The production of a sulfide having high specific activity and labeled with 35S...  
JPH0559716B2  
JPH05505723A
The invention relates to a process for converting peroxycarboxylic acids to carboxylic acids, the process comprising treating a peroxycarboxylic acid of the general formula: R-CO-OOH, wherein R is a linear or branched alkyl group, an ary...  
JPH05130881A
PURPOSE: To simply hydrolyze the subject derivative in an organic solvent without polluting environments by dissolving a carboxylic acid derivative in a slightly water- miscible organic solvent, saturating the solution with water, treati...  
JPH0536035B2  
JPH05125102A
PURPOSE: To purify carrageenins useful in the fields of drugs, food, and toiletry industrially and advantageously by heat-treating carrageenins with hydrogen peroxide under hydration conditions in the presence of an inactive, water- misc...  
JPH0533994B2  
JPH0527386B2  
JPH0521558B2  
JPH0514558B2
A method for producing optically active glycol derivatives by biochemical resolution which comprises contacting a racemic ester of the general formula 1(wherein R, is an aliphatic hydrocarbon group of 1 to 16 atoms, R2 is an aliphatic hy...  
JPH0513147B2  
JPH0539257A
PURPOSE: To obtain a new compound from a bacterium belonging to the genus Pseudomonas, useful as a compound for a medicine or agricultural chemical, having antimicrobial activity and antifungal activity. CONSTITUTION: A compound shown by...  
JPH054069B2
Indanyl compounds of the formula wherein R1 and R2 are hydrogen, fluorine or chlorine, is useful in the treatment of inflammatory and allergic diseases are prepared by fermenting indanyl compounds of the formula with a culture of Aspergi...  
JPH051787B2
A process for the preparation of 2-hydroxy-4-methylthiobutyric acid having improved color, odor and lower viscosity. 2-hydroxy-4-methylthiobutyronitrile is hydrolyzed with sulfuric acid having an initial strength of between about 50% by ...  
JPH0475000B2  
JPH04311394A
PURPOSE: To obtain the subject pyrocatecholic compounds such as L-DOPA, etc., simply and in high yields, useful for treatment of Parkinson's disease by carrying out the reaction of monophenolic compounds with oxygen under the presence of...  
JPH0462719B2  
JPH04248993A
PURPOSE: To efficiency obtain the subject compound useful as e.g. a raw material for renin inhibitors by emulsifying a racemic alkylsulfonylmethylhydrocinnamate in an aqueous medium followed by making a protease act on the above racemic ...  
JPH0446269B2
A novel alpha -D-mannosidase inhibitor, mannostatin, or its S-oxide, expressed by the following formula (1) wherein n denotes 0 or 1, and a process for producing it by culturing an actinomycete of the genus Streptomyces, said actinomycet...  
JPH0446119B2  
JPH04187632A
NEW MATERIAL:The compound of formula and its salt. Appearance, colorless or pale yellow oily substance; solubility, easily soluble in methanol, ethanol, ethyl acetate, chloroform and dimethyl sulfoxide and insoluble in water and hexane; ...  
JPH0412719B2  
JPH0440898A
PURPOSE: To produce α-hydroxy-4-methylthiobutyric acid industrially and advanta geously, by using a bacterium having hydrolyzing activity of α-hydroxy-4- methylthiobutyronitrile. CONSTITUTION: α-Hydroxy-4-methylthiobutyronitrile is co...  
JPH045438B2  
JPH0365953B2  
JPH0361424B2
The culture medium of the microorganisms antagonistic to plant pathogenic microorganisms are treated with an inorganic salt of a metal having a valency of 2 or more so as to give their cell walls positive charges, mixed with 5-10 w/w% of...  
JPH03163078A
NEW MATERIAL:A compound shown by formula I [R1 is H or 1-4C alkyl; Xb and Yb are H or OH; Z is amino, mono- or di-(1-4C alkyl)amino, etc.]. EXAMPLE: (3aR,4R,12aR,12bS)4-amino-2,3,3a,4,5-12,12a,12b-octahydro-6- hydroxyindolo[3,2,1-ij]ben...  

Matches 301 - 350 out of 386