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...
|