| Document |
Document Title |
|
JPH0672120B2 |
The invention concerns novel compounds of the formulawherein:X is selected from halogen, nitro, cyano, alkyl, substituted alkyl, hydroxy, alkoxy, substituted alkoxy, alkenyl, alkynyl, alkenyloxy, alkynyloxy, acyloxy, alkoxycarbonyl, alky...
|
|
JPH0672118B2 |
The invention concerns novel compounds of the formula IwhereinR' is selected from hydrogen, alkyl, alkenyl, alkynyl, substituted alkyl, acyl, alkylsulfonyl, benzenesulfonyl, substituted benzenesulfonyl, and an inorganic or organic cation...
|
|
JPH0672130B2 |
The invention concerns novel compounds of the formulawherein:X is selected from halogen, nitro, cyano, alkyl, substituted alkyl, hydroxy, alkoxy, substituted alkoxy, alkenyl, alkynyl, alkenyloxy, alkynyloxy, acyloxy, alkoxycarbonyl, alky...
|
|
JPH0672131B2 |
The invention relates to novel oxime ethers of the formula I (I) wherein R1 is hydrogen, halogen, lower alkyl, lower haloalkyl, lower alkoxy, lower haloalkoxy, lower alkylthio, lower haloalkylthio, lower alkylsulfinyl, lower alkylsulfony...
|
|
JPH0672129B2 |
|
|
JPH0672128B2 |
The invention concerns novel compounds of the formula IwhereinR' is selected from hydrogen, alkyl, alkenyl, alkynyl, substituted alkyl, acyl, alkylsulfonyl, benzenesulfonyl, substituted benzenesulfonyl, and an inorganic or organic cation...
|
|
JPH0672119B2 |
The invention concerns novel compounds of the formula Iwherein:W are selected from alkyl, alkenyl and alkynyl;X are selected from halogen, nitro, cyano, alkyl, substituted alkyl, hydroxy, alkoxy, substituted alkoxy, alkenyl, alkynyl, alk...
|
|
JPH0672177B2 |
|
|
JPH0667892B2 |
Compounds of the formula wherein Y is oxygen or sulfur are disclosed. These compounds are useful as hypotensive agents due to their angiotensin converting enzyme inhibition activity and depending upon the definition of R1 may also be use...
|
|
JPH0667893B2 |
The present invention relates to a process for the production of modified organic polyisocyanates containing urethane, carboxylic acid anhydride and biuret groups by reacting excess quantities of organic diisocyanates with a modifying ag...
|
|
JPH0667891B2 |
|
|
JPH06239785A |
PURPOSE: To obtain the subject compd. having low toxicity, useful as a therapeutic drug for heart failure, hypertention, or the like by condensing a specified compd. with a nucleophilic reagent of a specified formula in the presence of a...
|
|
JPH06234717A |
PURPOSE: To obtain a hydroxamic acid useful for preventing, controlling and improving the diseases caused by phytopathogenic bacteria.fungi. CONSTITUTION: The objective compound is expressed by formulae I and II [X, X1 are each O or S; R...
|
|
JPH0662511B2 |
|
|
JPH0662514B2 |
Novel polyquaternary ammonium compounds prepared from N,N'-bis(dialkylaminoalkyl)ureas, hydrochloric acid, epichlorohydrin and tertiary amines are useful as microbicides, corrosion inhibitors, debonding agents, flocculants, softeners, an...
|
|
JPH0662532B2 |
Disclosed are novel chemical compounds having the formula and processes for using compounds of formula I to obtain compounds having the formula
|
|
JPH0662530B2 |
|
|
JPH0662541B2 |
The invention provides N-acyl amino acid derivatives of general formula salts and esters thereof, wherein X represents an oxygen or sulphur atom, R<1> is an optionally substituted alkyl, alkenyl, cycloalkyl, aryl or aralkyl group or an o...
|
|
JPH0660153B2 |
|
|
JPH0660150B2 |
Novel polymerizable 3-aroyloxyphenyl carbamates such as 3-benzoyloxyphenyl 2-methacryloxyethylcarbamate form addition polymers which are useful as surface coatings for resinous (especially polycarbonate) articles. The coatings protect th...
|
|
JPH0660137B2 |
Compounds of Formula (I): wherein: Ar is phenyl, naphthyl, thienyl, fluorenyl, phenanthrenyl, dibenzo furanyl or a polynuclear group (A); in which a is 0, 1 or 2; B is (D)b(CH2)c(E)ewhere each of D and E is oxygen or sulphur, b and e are...
|
|
JPH0660152B2 |
Oxaluric acid derivatives of the formula (I): wherein each of R1 and R2, which may be the same or different, represents a hydrogen atom, an alkyl or cycloalkyl group, or R1 and R2 taken together with the adjacent nitrogen atom form a het...
|
|
JPH0655692B2 |
Cyclohexanecarboxylic acid derivs. of formula (I) are new. In (I) A= OR2 or N(R3)(R4), B= OH, NHOR1 or a metal or ammonium salt thereof; R= 1-6C alkyl or 3-6C cycloalkyl opt. substd. by halogen, 1-4C alkoxy or 1-4C alkylthio; R1= 1-6C al...
|
|
JPH0653713B2 |
Substituted peptide compounds of the formula are disclosed. These compounds are useful as hypotensive agents due to their angiotensin converting enzyme inhibition activity and depending upon the definition of X may also be useful as anal...
|
|
JPH06199761A |
PURPOSE: To obtain a new compound useful as a herbicide for controlling weeds causing problems in soil treatment and foliar treatment in upland field and water treatment in paddy field. CONSTITUTION: This compound of formula I (R1 and R2...
|
|
JPH06199759A |
PURPOSE: To prepare a compound useful as intermediates for synthesis of microbicides. CONSTITUTION: This compound of formula I (Z1 and Z2 are each H, a halogen, hydroxy, a 1-4C alkyl, a 1-4C alkoxy, phenoxy, nitro, cyano or the like; Z1 ...
|
|
JPH06199760A |
PURPOSE: To prepare the subject compd. by adding a mineral acid and an inert substance to an acetone oxime ether and distilling off until fractions don't contain acetone. CONSTITUTION: To a corresponding acetone oxime ether of the formul...
|
|
JPH0651671B2 |
1,3-Di(alkoxycarbonylamino)propanes of the general formula I (I) where R1, R2 and R3 can be identical or different and each is hydrogen, or an aliphatic, cycloaliphatic, araliphatic or aromatic radical, and R4 is an aliphatic, cycloaliph...
|
|
JPH06183960A |
PURPOSE: To obtain the subject suppressor, comprising a specific compound, having suppressing action on the production of 12-hydroxyeicosatetraenoic acid in a vascular wall and inhibiting and suppressing action on the hyperplasia of the ...
|
|
JPH06505506A |
PCT No. PCT/DE92/00865 Sec. 371 Date Jun. 11, 1993 Sec. 102(e) Date Jun. 11, 1993 PCT Filed Oct. 9, 1992 PCT Pub. No. WO93/07118 PCT Pub. Date Apr. 15, 1993.The invention relates to 9-substituted bicyclo[3.3.0]octane derivatives of formu...
|
|
JPH06505484A |
Compounds and a method useful for protection of tissue cells in a mammalian body from irreversible damages due to lactic acidosis caused by oxygen deficiency. The protection is achieved by administering a compound having a cell membrane ...
|
|
JPH06505485A |
Trifluorobutenoic acid, its methyl ester and a process of preparation thereof.
|
|
JPH06172882A |
PURPOSE: To efficiently and selectively separate and recover Pd by acidifying an aq. solution contg. Pd together with other metals and then bringing the acidified solution into contact with a specific ortho alkoxy-substituted phenyl oxim...
|
|
JPH06173058A |
PURPOSE: To provide a method for reducing the acid content of a hydroxylamine salt solution at the time of converting a hydroxylamine salt into a hydroxylamine. CONSTITUTION: This method comprises: (A) providing an electrolytic cell that...
|
|
JPH0645574B2 |
The invention relates to novel compounds of formula I: wherein the symbols have the significances given in the description, the synthesis thereof and to the use of compounds of formula I for the control of pests such as insects mites and...
|
|
JPH0645579B2 |
|
|
JPH0645582B2 |
Substituted peptide compounds of the formula are disclosed. These compounds are useful as hypotensive agents due to their angiotensin converting enzyme inhibition activity and depending upon the definition of X may also be useful as anal...
|
|
JPH0643344B2 |
The invention relates to a new process for preparing active esters or carboxylic acids, which consists in reacting a carboxylic acid, in the presence of an agent for binding hydrohalic acid, with a carbonate of formula: in which R1 denot...
|
|
JPH0643370B2 |
A process is described for the preparation of an optically active carboxylic acid or ester derivative thereof from a ketene and an optically active alpha -hydroxyester or an alpha -hydroxy amide.
|
|
JPH0643348B2 |
1-substituted tetralins of the formula I where n, R1, R2, R3, R4, R5 and R6 have the meanings stated in the description, and their preparation are described. The compounds are useful for the treatment of disorders.
|
|
JPH0641408B2 |
|
|
JPH0639457B2 |
|
|
JPH06145085A |
PURPOSE: To provide the new compounds useful as an anti-thrombus agent, an anti-ulcer agent and an anti-tumor agent. CONSTITUTION: The compounds of the formula I or their salts, e.g. 2- decarboxy-2-hydroxymethyl-9β-methyl-carbacyclin. T...
|
|
JPH0637453B2 |
|
|
JPH0637473B2 |
Compounds of formula (I): (wherein R¹ and R³ are organic groups, A is a direct bond, -CH₂-, -CH₂CH₂-, -CO-CH₂-, -O-CH₂- or -S-CH₂-, B is lower alkylene and n is l-3) are valuable hypotensive agents which may be prepared by ...
|
|
JPH06135918A |
PURPOSE: To facilitate the removal of water or an aqueous solution of hydrochloric acid which has been difficult to separate according to a conventional separating method and enable the recovery of a solvent used as an azeotropic removin...
|
|
JPH06135925A |
PURPOSE: To provide the substituted ethanediimidamides useful as intermediates for preparing histamine H2-receptor antagonists which are effective in treating a hypersecretion abnormality such as gastric ulcer or the like. CONSTITUTION: ...
|
|
JPH06504034A |
Heterocyclic anthracyclinone and anthracycline derivatives are described, which are useful in the treatment of cancer and tumors, such as breast cancer, leukemia, lung cancer, colon cancer, ovarian cancer, renal cancer, CNS cancer and me...
|
|
JPH0635444B2 |
Disclosed herein are adrenergic compounds represented by the formula wherein m is 0, 1 or 2; R1, R2, R3 are taken from the group consisting of hydrogen, hydroxy, loweralkyl, loweralkoxy, halo, or NHSO2R wherein R is taken from the group ...
|
|
JPH06128205A |
PURPOSE: To provide the method for preparing substituted or unsubstituted N-hydroxy-2-aminobutane diacid derivatives which can be converted into pyridine and quinoline derivatives by first converting the diacid derivatives into 2- aminob...
|
