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JP4175112B2 |
There are provided a fluorine-containing ethylenic monomer having hydroxyl group or fluoroalkyl carbonyl group and represented by the formula (1): and the formula ( 14): respectively, wherein X<1> and X<2> are the same or different and e...
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JP4174788B2 |
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JP2008260756A |
To provide a method for producing an alkenylaryl by subjecting an aryl alcohol raw material liquid containing titanium as an impurity to dehydration reaction in the presence of an alumina-based dehydration catalyst, which has an excellen...
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JP2008260714A |
To provide a method for industrially efficiently producing optically active haloalcohols which are intermediates of an optically active ketene dithioacetal derivative useful as an antifungal agent.The method for producing the optically a...
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JP4171965B2 |
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JP4173569B2 |
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JP4169801B2 |
A reductive system including a silane, preferably PMHS, and an active zinc compound, which is monomeric and not a hydride, wherein a reduction of a carbonyl substrate to a corresponding alcohol is achievable.
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JP2008247836A |
To provide a method for producing an alcohol highly selectively using a phosphine compound that can be easily recovered and reused.The method for preparing an alcohol represented by formula (III) is characterized by causing a conjugated ...
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JP4164318B2 |
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JP4163837B2 |
2-Methyl-2-indanemethanol derivatives (I) are new. Compounds of formula (I) are new: R<1>-R<4> = H or (un)saturated 1-3C alkyl, but not all H. Independent claims are also included for the following: (1) a process for preparing (I); (2) 2...
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JP4159700B2 |
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JP4153302B2 |
A catalytic transfer hydrogenation process is provided. The catalyst employed in the process is a metal hydrocarbyl complex which is coordinated to defined bidentate ligands substituted with at least one group selected from an optionally...
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JP4154958B2 |
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JP4155720B2 |
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JP2008214194A |
To provide a catalytic reduction method and a coupling method useful for the synthesis of organic compounds and giving little load on the environment.A substrate and a heterogeneous platinum-group catalyst are mixed and stirred in a hydr...
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JP4152505B2 |
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JP4151829B2 |
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JP2008201783A |
To provide a class of chemical compounds useful as efficacious drugs in the treatment of sickle cell disease and diseases characterized by unwanted or abnormal cell proliferation.The active compounds are substituted triaryl methane compo...
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JP4143683B1 |
This invention offers 6,8,10-undecatrien-3-ol and 6,8,10-undecatrien-4-ol. These compounds possess not only woody green note, but also fruity note rich in naturality and freshness, and aroma compositions blended therewith are useful for ...
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JP4144814B2 |
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JP4138403B2 |
The present invention concerns a compound of formula wherein the R groups represent, simultaneously or independently, a hydrogen atom or a methyl group, R' represents a hydrogen atom or an acetyl group, G represents a cyclopentyl or a cy...
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JP4140523B2 |
A solvent contains cycloalkylalkylether (1). A solvent contains cycloalkylalkylether of formula (1), R 1>-O-R 2> (1) R 1>optionally substituted cyclopentyl or cyclohexyl; R 2>optionally substituted 1-10C alkyl or 3-8C cycloalkyl. Indepen...
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JP2008189672A |
To provide a new compound used for synthesizing liquid crystal components.The compound has the structure: w-A-x-CY-Z(CF3), (wherein CY is cyclohexane or substituted cyclohexane), exemplified by 4-trifluoromethyl-4-methylcarboxy-4'-propyl...
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JP4135639B2 |
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JP4133334B2 |
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JP4133337B2 |
A carrier for carrying an osmium oxide comprising an aromatic polyolefin having a group shown by the general formula Ä1Ü: - A'-O(-A-O)n-R (wherein, A is an alkylene group; A' is a direct link or an alkylene group; R is an aryl group; a...
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JP2008530196A |
The present invention provides a compound having one of the following formulae: R and R1 are each independently H or C1-5 alkyl provided that in formula (I) when R is methyl, R1 is H or C2-5 alkyl. R2 has from 1 to about 12 carbon atoms ...
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JP4130439B2 |
Alkyl phenyl alkanols, alkyl phenyl alkanol derivatives and detergent compositions comprising same. More specifically, alkyl phenyl alkanols and alkyl phenyl alkanol derivatives that provide enhanced primary biodegradability elative to c...
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JP4129993B2 |
Novel compounds are provided which are inhibitors of MTP and thus are useful for lowering serum lipids and treating atherosclerosis and related diseases, and have the structure (I) or (IA) or (IB) including pharmaceutically acceptable sa...
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JP2008174470A |
To provide a method for producing a Grignard reagent from a fluorine-containing chlorobenzene compound and magnesium, by which the product is easily obtained by improving low reactivity of the fluorine-containing chlorobenzene compound a...
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JP2008174472A |
To provide a method for producing a Grignard reagent from a carbon substituent-containing chlorobenzene compound and magnesium, by which the product is easily obtained by improving low reactivity of the carbon substituent-containing chlo...
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JP2008174426A |
To provide a molybdenum-containing oxide material retaining high activity by suppression of Mo scattering, i.e., improving remarkably catalyst durability, and a method for producing the same.The molybdenum-containing oxide material has a...
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JP2008174471A |
To provide a method for producing a Grignard reagent, and to provide a method for producing a Grignard reaction product.This method for producing the Grignard reagent from a chloronaphthalene compound and the magnesium as raw materials i...
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JP2008528528A |
The present invention relates to a process for preparing cyclohexanone and cyclohexanol, said process comprising (a) neutralising acids and/or carbon dioxide present in an organic solution further comprising cyclohexylhydroperoxide by mi...
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JP4125672B2 |
Novel halophenyl derivatives of the general formula (I), wherein R1 is halogen, a leaving group or 1H-1,2,4-triazol-1-yl and R2 is ethynyl or carboxy, X1 is halogen and X2 and X3 are each independently hydrogen or halogen, and their manu...
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JP4128738B2 |
Layered double hydroxides exchanged with osmate of the formula [MII(1-x)MIIIx(OH)2] [OsO42-]x/2.zH2O wherein MII is a divalent cation selected from the group consisting of Mg2+, Mn2+, Fe2+, Co2+, Ni2+, Cu2+, Zn2+ and Ca2+ and MIII is a t...
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JP4124414B2 |
A heterogeneous liquid-phase process for the hydrogenation of aldehydes of Formula (I) and (III) to the corresponding alcohols of Formula (II) and (IV) which process comprises contacting alcoholic or aqueous-alcoholic solution of aldehyd...
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JP4122603B2 |
A process for producing dichloroacetoxypropane comprising reacting allyl acetate with chlorine in a gaseous phase in the presence of a catalyst. The dichloroacetoxypropane obtained may be converted to dichloropropanol and epichlorohydrin.
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JP2008525395A |
A process for the preparation of a compound of Formula (1) wherein Ar represents an optionally substituted hydrocarbyl or an optionally substituted heterocyclyl group comprising an aromatic moiety; and R1 and R2 each independently repres...
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JP2008525474A |
Improved citral and citronellal derivatives, and fragrance and flavorings including the derivatives, that have a longer useful shelf life than citral and citronellal and/or fragrances and flavoring including citral and citronellal, are d...
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JP2008162984A |
To provide a novel compound useful as a monomer for a polymer compound utilizable as a component of a resist composition and a novel compound useful for manufacturing the compound.The compound is represented by general formula (I) [where...
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JP4117468B2 |
To provide a polymer having a main chain of a fluorinated alicyclic structure, which has a high Tg and which has a functional group concentration sufficient to exhibit the characteristics, and a process for its production. A fluoropo...
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JP2008156367A |
To provide a method of commercially advantageously producing a cycloalkyl alkyl ether compound useful as a novel cleaning solvent, a reaction solvent, an extraction solvent, a solvent for electronic and electrical materials, a remover us...
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JP4116891B2 |
To provide a reducing catalyst excellent in handling, safety end durability and capable of performing hydrogenation reaction selectivity, its manufacturing method and a selective hydrogenation method. This reducing catalyst 10 is obtaine...
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JP4111680B2 |
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JP2008519798A |
The invention relates to an enantiomerically enriched chiral compound comprising a transition metal M, which comprises four, five or six coordinating groups of which at least one pair is linked together to form a bidentate ligand, in whi...
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JP4099226B2 |
The present invention provides methods and product for inhibiting mammalian cell proliferation. Compounds that are anti-mycotics and that inhibit the Ca<++>-activated potassium channel of erythrocytes have been modified for use in the pr...
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JP4096582B2 |
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JP2008517990A |
There is provided a process for the de-enrichment of enantiomerically enriched compositions which comprises reacting an enantiomerically enriched composition comprising at least a first enantiomer or diastereomer of a substrate comprisin...
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JP4090078B2 |
A catalytic transfer hydrogenation process is provided. The catalyst employed in the process is a metal cyclopentadienyl complex which is coordinated to defined bidentate ligands. Preferred metals include rhodium, ruthenium and iridium. ...
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