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Document Title |
JPH05262711A |
PURPOSE: To prepare new butyric acid amides effective for controlling insects and ticks particularly in rice, cotton, vegetable and fruit crops and forests as agents for controlling harmful insects and furthermore effective for normal se...
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JPH0568463B2 |
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JPH0568472B2 |
Substituted ethanediimidamides of the formula wherein m is 0-2, n is 2-5, Z is O, S or methylene, R<1> is H or alkyl and A is exemplified as piperidino - or pyrrolidino - methylphenyl, dimethylaminomethyl-furyl or thienyl, or piperidinom...
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JPH05246969A |
PURPOSE: To provide a phenylalanineammonia lyase inhibitor containing, as active ingredient, an aminoxyfatty acid. CONSTITUTION: The objective inhibitor containing, as active ingredient, a compound of formula I [R1 and R2 are each H or c...
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JPH0566939B2 |
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JPH0566381B2 |
There are described compounds of formula:in which X (or X') = H, F, Cl and X' (or X) = F, Cl;with R' = H, Cl, Br, F an optionally halogen-substituted alkyl C1-C3;R' = halogen, an optionally halogen-substituted alkyl C1-C3;R4 =H or R3;R' ...
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JPH0566380B2 |
An I.D.R. process for the manufacture of urea, comprising two subsequent loops, wherein: A) In the first (high pressure) loop the solution coming from the synthesis zone contains, after the first isobaric strip per (E1), a strong NH3 exc...
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JPH0564944B2 |
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JPH0561263B2 |
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JPH0560460B2 |
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JPH0560461B2 |
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JPH0560456B2 |
N-acetonyl-substituted-amides of the formula: …… wherein A is a certain, optionally ring-substituted heterocycle, phenylalkyl, phenylalkoxy, naphthyl, cycloalkyl, alkoxyalkyl, alkyl, haloalkyl or alkenyl group; X, Y and Z are selecte...
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JPH05221916A |
PURPOSE: To obtain a new α-(5-aryloxy-naphthalen-1-yl-oxy)carboxylic acid deriv. utilized as a defoliant, a dehydrator, a broadleaf plant killer, etc. CONSTITUTION: The α-(5-aryloxy-naphthalen-1-yl-oxy)carboxylic acid deriv. is a compd...
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JPH0558629B2 |
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JPH0558626B2 |
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JPH0558621B2 |
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JPH0558426B2 |
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JPH0557978B2 |
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JPH0556335B2 |
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JPH0555496B2 |
Compounds of the general formula where X is fluorine, chlorine, ethyl or n-propyl, and the salts of these compounds, and herbicides containing the compounds or their salts.
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JPH0554947B2 |
A heat developable light-sensitive material containing a compound represented by formula (I) or (II) (I) (II) wherein R1 and R2 each represents a hydrogen atom, an alkyl group, a cycloalkyl group, an alkenyl group, an alkynyl group, an a...
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JPH05201944A |
PURPOSE: To provide an acylaminobenzamide compd. which exhibits fungicidal activity to the diseases of a wide range of plants and is active to the kinds of pathogens particularly known as fungi. CONSTITUTION: A compd. of formula I [A and...
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JPH0552821B2 |
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JPH0550502B2 |
PURPOSE:To obtain urea from ammonia and carbon dioxide with reduced power consumption at a low cost, by mixing a recovered liquid from a purification step with liquid ammonia for synthetic raw material, raising the pressure of the mixtur...
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JPH0543697B2 |
Polypeptide derivatives containing 5-amino-2,5-disubstituted-4-hydroxypentanoic acid residues are of the formula:wherein, for example in a preferred embodiment R is t-butyloxycarbonyl, m and n are each 0 or 1, their sum being at least 1;...
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JPH0541628B2 |
1-[2-(2,4-Dichlorophenyl)-pentyl]-1H-1,2,4-triazole can be produced, in a novel, simple, economical and isomer-free form, by reacting 2-(2,4-dichlorophenyl)-valeronitrile, in the presence of hydrogen, an acid and a hydrogenation catalyst...
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JPH05148208A |
PURPOSE: To produce an amine derivative useful as an intermediate for pharmaceuticals by using a new compound derived from a nitrone compound and an organic acid halide as a starting raw material and reacting the material with a nucleoph...
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JPH0533946B2 |
Amino acid salt having at least one unblocked amino group and comprising at least one cation which has a nitrogen cationic atom is reacted with 1-(tertiary-alkoxycarbonyl)imidazole in the liquid phase and in the presence of essentially i...
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JPH0531540B2 |
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JPH0531543B2 |
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JPH0531542B2 |
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JPH0531541B2 |
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JPH05112501A |
PURPOSE: To obtain a new butadiene derivative, having the high charge transfer ability, excellent in light stability and capable of providing electrophotographic photoreceptors, having high sensitivity and improved in durability. CONSTIT...
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JPH05112502A |
PURPOSE: To obtain a new butadiene derivative, having the high charge transfer ability, excellent in light stability and capable of providing electrophotographic photoreceptors, having high sensitivity and improved in durability. CONSTIT...
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JPH05105657A |
PURPOSE: To provide novel antibiotics useful for the theraspies of mycotic infectious diseases by Candida, Aspergillus, etc. CONSTITUTION: The objective antibiotics are expressed by formula I (X is of formula II or III) [i.e., WAP-5044A ...
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JPH0528698B2 |
A process for preparing urethanes by reacting a solution of a nitrogen-containing organic compound and a hydroxyl-containing organic compound with carbon monoxide in the presence of a halide-free ruthenium catalyst is disclosed. In the p...
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JPH05105658A |
PURPOSE: To provide a new cyclohexenenone oxime ether useful as herbicides attaining the herbiciding objective with an amount less than the known substances and having high selectivity. CONSTITUTION: The compound of formula I, e.g. 2-[1-...
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JPH0528210B2 |
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JPH0528219B2 |
PURPOSE:To prepare high-quality urea while suppressing progress of hydrolysis and formation of biuret, by dividing the shell side of a heat exchanger of shell and tube type used in a stripping decomposition device into plural fractions, ...
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JPH0528218B2 |
PURPOSE:The heat energy which is released, when a mixed gas resulting from the stripping of the liquid fraction from the urea synthesizer, is reliquefied, is directly used to heat the stripping stage whereby urea is produced with greatly...
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JPH0528220B2 |
A compound having the formulawherein R1 represents halogen or methyl; R2 represents hydrogen or halogen; each of R3 and R4 represents halogen; and each of X and Y represents oxygen or sulfur.The compound is useful as insecticide.
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JPH0527618B2 |
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JPH0597812A |
PURPOSE: To provide a novel 1-alkoxy-1,3-diazacycloalkane derivative having an improved pesticidal effect (effectiveness and effectiveness persistence). CONSTITUTION: A compound expressed by formula I ((n) represents 0 or 1, R1 is alkyl,...
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JPH0526775B2 |
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...
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JPH0526776B2 |
1. Process for preparing vinyl carbamates of the formula I : see diagramm : EP0104984,P29,F1 in which R1 and R2 , which may be identical or different, denote a hydrogen atom, or a substituted or unsubstituted, saturated or unsaturated al...
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JPH05502036A |
(57) [Summary] Since this publication is application data before electronic filing, summary data is not recorded.
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JPH0524896B2 |
The invention describes a process for the preparation of N,o-substituted mono- and/or polyurethanes of formula R1[-NHCOOR2]n, in which R1 is an aliphatic, cycloaliphatic, aromatic, araliphatic, or heterocyclic radical, which may be subst...
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JPH0524145B2 |
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JPH0524142B2 |
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JPH0524144B2 |
There are disclosed novel oxamic acid esters substituted on the nitrogen atom and corresponding to the formula I (I) the production thereof, their use for controlling pests, and pesticidal compositions containing these oxamic acid esters...
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