Abstract: The invention relates to a process for preparing quinoline-substituted carbonate and carbamate compounds, which are important intermediates in the synthesis of 6-O-substituted macrolide antibiotics. The process employs metal-catalyzed coupling reactions to provide a carbonate or carbamate of formula (I) or (II) or a substrate that can be reduced to obtain the same.

Abstract: A process for the production of an aromatic carbonate is disclosed. Accordingly, an aromatic hydroxy compound is reacted with carbon monoxide and oxygen in the presence of a platinum group metal catalyst, a co-catalyst, a base, and optionally a quaternary salt as well as an inert organic solvent. The reaction is carried out under conditions whereby the inert organic solvent forms an azeotrope with the water arising during the reaction. The azeotrope is then removed from the reaction mixture.

Abstract: Efficient synthetic methods towards mixed aliphatic carbonates through the three component couplings of aliphatic alcohols, alkyl halides and carbon dioxide in the presence of cesium carbonate and tetrabutylammonium iode (TBAI). Due to their enhanced nucleophilicities, cesium alkoxides are smoothly incorporated into CO2, allowing for mild reaction conditions such as ambient temperatures and short reaction durations. Various primary and secondary substrates are compatible under the standard conditions, offering high yields, while chiral templates such as &agr;-hydroxy carbonyls are resistant to racemization.

Abstract: Polyester based polycarbonate (meth)acrylates prepared by the reaction of a alkylene or arylene diol polycarbonate with an anhydride or its dicarboxylic acid to form a carboxyl terminated diester, reacting the diester with a diglycidyl ether and an acrylic or methacrylic acid to form an acrylate terminate polymer which is useful for radiation cured coatings which have superior adhesion and reverse impact strength when applied to plastic substrates.

Abstract: Compounds of the Formula 1, Formula 2, Formula 3 and Formula 4 wherein the symbols have the meaning assigned to them in the disclosure have retinoid-like biological activity.

Abstract: An organic solvent is separated from a waste stream comprising hydrofluoric acid, an organic solvent and etchant contaminants. The process comprises separating the hydrofluoric acid by subjecting the waste stream to at least one of the following processes: ion exchange; extraction of the hydrofluoric acid; electrophoresis; converting the hydrofluoric acid to an insoluble salt; to thereby obtain a first composition containing the hydrofluoric acid and a second stream containing the organic solvent and being substantially free of the hydrofluoric acid; and then distilling the second stream to recover the organic solvent free of the etching contaminants.

Abstract: This invention provides a process for the selective esterfication of a tertiary alcohol(I) by an acid anhydride(II) to produce corresponding tertiary ester(III) and carboxylic acid(V), using a reusable solid catalyst(IV) comprising one or more halides of indium, gallium, zinc and iron. The process comprises: (i) contacting a mixture of (I) and (II) in the absence or presence of a non aqueous solvent with the fine particles of (IV) in a stirred batch reactor provided with a reflux water condenser at atmospheric pressure at the reaction conditions, such that the mole ratio of (II) to (I) is in the range from about 0.1 to about 10.0; the weight ratio of (IV) to (I+II) is in the range from about 0.005 to about 0.5; the reaction temperature is below about 80° C., and the reaction period is in the range from about 0.1 h to about 50 h; (ii) removing the solid catalyst(IV) from the reaction mixture by filtration; and (iii) reusing the separated solid catalyst for subsequent batch of the process.

Abstract: A method for preparing carbonates includes reacting an alkylene oxide with carbon dioxide in the presence of a catalyst and a non-protic solvent. The method further includes having the boiling point of the solvent greater than about 70° C., and removing the solvent from the reaction product. The solvent used in the various forms of the present invention can be glyme, diglyme, tetraglyme, cumene, toluene, tetrahydofuran, cyclohexanone, ethylbenzene, aromatic hydrocarbons, or ethers. The catalyst used can be a tetraalkyl ammonium halide, such as tetraethyl ammonium bromide. The alkylene oxide that can be used in the invention can include Bisphenol A, Bisphenol B, Bisphenol F, alkylene oxides that have alkyl substituent groups, alkylene oxides that have aryl substituent groups, and alkylene oxides that contain both alkyl and aryl substituent groups. An essentially solvent free carbonate can be prepared by flash removal of the solvent.

Abstract: A process for producing dialkyl carbonates, such as dimethyl carbonate, from the reaction of a primary alcohol with urea in the presence of a catalyst which is a complex compound represented by R2Sn(OCH3)2·&khgr;L, wherein R=CnH2n+1, n=1 to 12, &khgr;=1 or 2, and L is oxygen atom containing organic complexing agent which is carried out by conducting the reaction continuously under reactive distillation conditions wherein the product DMC is stripped from the reaction mixture with methanol and further including the recovery of product dimethyl carbonate (DMC) made in the process by contacting a stream containing the DMC, such as a azeotropic mixture with methanol, with diethyl oxylate under conditions of extractive distillation to selectively separate the DMC from methanol.

Abstract: An integrated process for the production of a dialkyl carbonate and a diol from an alkylene oxide, carbon dioxide and an aliphatic monohydric alcohol is described in which an alkylene oxide is first reacted with carbon dioxide in the presence of a carbonation catalyst to provide a corresponding cyclic carbonate and impurities and the cyclic carbonate, which contains the impurities, is then reacted with an aliphatic monohydric alcohol in the presence of a transesterification catalyst to provide a corresponding dialkyl carbonate and diol.

Abstract: A method for making a vinyl carbonate represented by the formula (I):

Abstract: The present invention relates to novel retinol derivatives having the formula (I): and to processes for preparing them. The invention also relates to the use of these compounds in or for the preparation of compositions intended for treating conditions of the skin or scalp, for example in preventing or combating acne and/or chronological or actinic ageing of the skin.

Abstract: The synthesis of taxol and other tricyclic and tetracyclic taxanes.

Abstract: A process for producing a dialkyl carbonate which comprises performing reaction of allophanate represented by the following general formula (1) and an alkyl alcohol represented by the following general formula (2) as raw materials, thereby producing a dialkyl carbonate represented by the following general formula (3).

Abstract: Bromide source such as alkali metal bromide, alkaline earth metal bromide, or onium bromide, present as part of a catalyst mixture in an organic oxidative carbonylation mixture further comprising diaryl carbonate and a hydroxyaromatic compound, is often at least partially converted to organic bromide such as bromophenols. The bromide source can be recycled after reaction through treatment with an aqueous acidic bromide solution such as hydrogen bromide, preferably after removal of a major proportion of hydroxyaromatic compound such as phenol.

Abstract: The invention relates to fragrance precursors, In particular, the invention relates to the use of several classes of compounds which may act as fragrance precursors, e,g., in cosmetic products such as deodorants and antiperspirants and in laundry products such as detergents and fabric softners. These compounds are odorless, but upon contacting the skin as example, in skin care compositions or in personal care compositions, produce fragrances. The compounds also produce fragrances when used in the presence of lipases, e.g. as used in (laundry) detergents, thus providing a prolongation of the fabric scenting effect. The compounds under consideration are compounds of the formula I: The substituents are defined in the specification.

Abstract: A method and catalyst system for economically producing aromatic carbonates from aromatic hydroxy compounds. In one embodiment, the present invention provides a method of carbonylating aromatic hydroxy compounds by contacting at least one aromatic hydroxy compound with oxygen and carbon monoxide in the presence of a carbonylation catalyst system that includes a catalytic amount of an inorganic co-catalyst containing lead and a catalytic amount of an inorganic co-catalyst containing titanium. In various alternative embodiments, the carbonylation catalyst system can include an effective amount of a palladium source and an effective amount of a halide composition. Further alternative embodiments can include catalytic amounts of various inorganic co-catalyst combinations.

Abstract: A method of recovering benzyl alcohol, gamma butyrolactone, or propylene carbonate from an impure effluent stream of an industrial process is provided. The effluent waste stream contains greater than about 10 percent by weight of monomeric units that are reacted to form larger oligomers and polymers. The first step in the recovery process involves polymerizing the monomeric units present in the effluent waste stream under conditions effective to reduce the concentration of monomeric units in the waste stream to less than about 10 weight percent. The waste stream then is fed to a first separation stage where it is separated into (i) a gaseous stream of water, soluble gases, and volatile contaminants and (ii) a suspension comprising the high boiling solvent, semi-volatile materials, and non-volatile contaminants and materials. Then the dewatered, low vapor pressure, high boiling solvent-containing suspension is either distilled or evaporated to separate the high boiling solvent from non-volatile materials.

Abstract: Compounds of the invention having general formula ##STR1## are useful reagents for protecting amine, guanidine, amidine or hydroxyl groups during organic synthesis. In particular, compounds are useful during oligonucleotide synthesis to protect nucleobase amines as well as tethered amines used for attaching functional moieties to oligonucleotides.

Abstract: A process for preparing organic carbonates, such as dimethyl carbonate, without the use of phosgene and with a high yield and selectivity to the desired carbonate, by reacting a formaldehyde-acetal with a source of oxygen, in the presence of a catalyst.

Abstract: A method of recovering solvents from an impure effluent stream of an industrial process. The effluent waste stream contains less than about 10 percent by weight of monomeric units that are reacted to form larger oligomers and polymers. The waste stream contains dissolved polymers, polymeric particles, and the hydrolysis, oxidation and/or other decomposition products of one of the solvents. In one embodiment, the first step involves filtering particulate matter from the waste stream. In another embodiment, the filtering step is omitted. The filtered or unfiltered waste stream is fed to a first separation stage for separation into (i) a gaseous stream of water, soluble gases, and volatile contaminants and (ii) a suspension comprising the solvent, water, semi-volatile and non-volatile contaminants, and photoresist products.

Abstract: (Het)aryloxy-, -thio- and -aminocrotonates of the formula I ##STR1## where the substituents have the following meanings: U is oxygen, sulfur or amino;V is oxygen, sulfur, amino or alkylamino;X, Y and Z independently of one another are .dbd.N-- or .dbd.CR.sup.3 --;R.sup.1 and R.sup.2 independently of one another are alkyl;R.sup.3 is hydrogen, cyano, nitro, halogen, alkyl, haloalkyl, alkoxy, haloalkoxy, alkylthio and haloalkylthio; andR.sup.4 is an organic radical which is bonded to the skeleton directly or via an oxy, mercapto, amino, carboxyl or carbonylamino group,process for their preparation, and their use.

Abstract: The present invention relates to cyclic terpyridine-lanthanide complexes having 8 nitrogen atoms and 10 carbon atoms in the macrocycle and containing a functional group in the terpyridine moiety. The invention also relates to a process for the preparation of cyclic terpyridine-lanthanide complexes through the condensation of terpyridine hydrazines with pyridine-2,6-dialdehydes or -ketones. The compounds can be complexed with oligonculeotides and are useful in the sequence-specific cleavage of RNA.

Abstract: A process for producing a carbonic acid diester, which comprises carrying out a reaction in a vapor phase of an alcohol, carbon monoxide and oxygen in the presence of a catalyst in a fluidized-bed reactor so that an oxidative carbonylation of the alcohol occurs, thereby obtaining a carbonic acid diester, wherein a heat of reaction is removed by the latent heat of vaporization of the alcohol as a raw material. In the process, for example, either at least part of the alcohol may be directly fed in liquid phase into the fluidized bed or cooling pipes are disposed in the fluidized bed and at least part of the alcohol is introduced in liquid phase into the cooling pipes as a heat transfer medium so that the liquid alcohol is vaporized and fed into the fluidized-bed reactor. Carbon monoxide may be introduced together with the liquid alcohol into the cooling pipes.

Abstract: A process for producing a carbonic acid diester, a method of removing CO.sub.2 and an absorbent for CO.sub.2 and an apparatus therefor are provided and are capable of selective removing of CO.sub.2 by absorption from a CO-containing gas admixed with CO.sub.2 which is recovered from a reactor to thereby enable recycling CO to the reactor for use. The invention is characterized by (1) carrying out a reaction of an alcohol, carbon monoxide (CO) and oxygen in a reactor and withdrawing a gas (i) which contains CO and CO.sub.2 produced as a by-product of the reaction from the reactor; (2) contacting the withdrawn gas (i) with an alcohol solution so that at least part of the CO.sub.2 contained in the gas (i) is absorbed by the alcohol solution and removed from the gas (i), thereby obtaining a CO-containing gas (ii), and (3) recycling the CO-containing gas (ii) to the reactor. It is preferred that the gas (i) is subjected to vapor-liquid separation and a separated gas is contacted with the alcohol solution.

Abstract: Known (R)-1-aryl-alkylamines of the formula ##STR1## in whichR.sup.1 and Ar have the meanings indicated in the description, are prepared by a new process, which comprisesa) reacting a racemate of an ethyl or methyl 2-aryl-alkanoate of the formula ##STR2## with ammonia in the presence of a lipase which is suitable for the cleavage of esters, in the presence of a diluent,b) separating off from the reaction mixture the resulting (R)-2-aryl-alkanamide of the formula ##STR3## and then reacting it with sodium hypochlorite or sodium hypobromite in the presence of water.

Abstract: A porous lithium aluminate carrier for catalyst has a spinel structure which has a mean pore diameter in the range of 40 to 1,000 angstroms and a total pore volume in the range of 0.2 to 1.5 mL/g. The porous lithium aluminate carrier can be used for supporting a catalyst compound containing a platinum group metal. The catalyst on the carrier can be favorably employed for promoting catalytic reaction of a nitrite ester and carbon monoxide to prepare a carbonate diester such as dimethyl carbonate.

Abstract: Carbonates with aromatic ester groups may be produced by reacting aromatic monohydroxy compounds with phosgene or with chlorocarbonates of aromatic monohydroxy compounds, wherein a temperature in the range from 50.degree. to 450.degree. C. and a pressure in the range from 0.05 to 20 bar are used in the presence of hard materials with metal-like properties (ceramic precursors) as heterogeneous catalysts.

Abstract: A process for making a dialkyl carbonate which comprises reacting urea with a first alcohol in a carbamate reactor at a temperature and pressure sufficient to convert said urea to an alkyl carbamate; and reacting the alkyl carbamate with a second alcohol in the presence of a dialkyl isocyanato alkoxy tin catalyst or derivatives in a carbonate reactor at a temperature and pressure sufficient to convert the alkyl carbamate to a dialkyl carbonate, wherein the molar ratio of alkyl carbamate to second alcohol is in the range between about 2:1 to about 10:1 and wherein dialkyl carbonate is present within the carbonate reactor in an amount between about 1 to about 3 weight %, based on total alkyl carbamate and second alcohol content, and wherein the second alcohol is either the same as or different from the first alcohol or a mixture of alcohols.

Abstract: Dimethyl carbonate (DMC) is prepared by continuous gas reaction of carbon monoxide and methyl nitrite a heterogeneous catalyst comprising a platinum at 50.degree. to 170.degree. C. under 1 to 5 bar.

Abstract: The present invention is concerned with a process for the manufacture of optically active compounds of the formula ##STR1## wherein R signifies lower alkyl, lower alkoxy, phenyl, benzyl or --NR.sub.2.sup.1, R.sup.1 signifies lower alkyl, phenyl, benzyl or hydrogen and * signifies an optically active center, by asymmetrically hydrogenating an enol derivative of ketoisophorone of the formula ##STR2## wherein R has the significance given above, in the presence of a rhodium complex of an optically active diphosphine ligand.

Abstract: A process for producing dimethyl carbonate is carried out by a first step of catalytically reacting carbon monoxide with methyl nitrite to produce dimethyl carbonate; a second step of absorbing dimethyl carbonate contained in a gas fraction withdrawn from the first step by dimethyl oxalate; a third step of regenerating methyl nitrite by contacting nitrogen monoxide contained in a gas fraction withdrawn from the second step with a molecular oxygen-containing gas and methyl alcohol; a fourth step of collecting dimethyl carbonate by distilling a liquid fraction withdrawn from the second step; and a fifth step of producing and recovering methyl nitrite from a purge gas consisting of a minor portion of a gas fraction withdrawn from one of the second step and the third step by bringing the purge gas together with an ammonia-oxidation product gas into contact with methyl alcohol in a methyl nitrite-recovering column, to thereby produce and recover methyl nitrite contained in the recovering column with a high efficie

Abstract: A method is described enabling HCl and possible entrained CuCl particulate to be removed from a gas-vapor stream leaving a dimethylcarbonate synthesis reactor. The contaminant removal is effected by one of the process fluids used in a small quantity.

Abstract: This invention pertains to compounds represented by formula (1): ##STR1## wherein R is selected from the group consisting of branched and unbranched lower-alkyl and lower-cycloalkyl groups having from 1 to 10 carbon atoms. The present invention also provides smoking compositions, and methods for flavoring smoking compositions, which incorporate the novel alkyl sclareol diol carbonates of the invention.

Abstract: Dimethyl carbonate is obtained with a high selectivity and great constancy over time by reacting carbon monoxide with methyl nitrite in a continuous gas phase reaction in the presence of a heterogeneous catalyst prepared by the application to a suitable support of one or more palladium compounds of the formula[Pd(N(R.sup.1, R.sup.2, R.sup.3)).sub.n ]X.sup.1.sub.2 (I) ,wherein R.sup.1, R.sup.2, R.sup.3, X.sup.1 and n are as defined in the disclosure, optionally in combination with one or more promoters from the group consisting of the elements Fe, Co, Ni, V, Nb, Mo, Ta, Ti, Cu and Cr, the rare earths and/or compounds thereof, and/or with one or more promoters from the group consisting of alkali metal and alkaline earth metal halides.

Abstract: Dialkyl carbonates can be prepared by reacting carbon monoxide with alkyl nitrites in a continuous gas phase reaction in the presence of a heterogeneous platinum metal catalyst, the activity of this catalyst being maintained by the addition of small amounts of halogen. The dialkyl carbonates are thus formed with almost quantitative selectivity and no deactivation of the catalyst occurs.

Abstract: A process of preparing diaryl carbonates, such as diphenyl carbonate, and aryl haloformates, such as phenyl chloroformate. The process involves contacting phenol or a substituted phenol with a carbonyl halide, such as phosgene, in the presence of a phosphorus-containing catalyst. The catalyst is selected from alkyl phosphates, aryl phosphites, aryl phosphates, organic phosphinites and phosphinates, organic pyrophosphates, inorganic phosphorous and phosphoric acids, and phosphorus oxides.

Abstract: A carbonic acid diester is produced, at a high reaction rate with a high selectivity and stability, by catalytically reacting carbon monoxide with a nitrous acid ester, preferably in a gas phase, in the presence of a solid catalyst composed of a solid carrier and a catalytic solid material deposited on the carrier and comprising:(1) a first catalyst component comprising at least one member selected from the group consisting of platinum group metals and compounds thereof;(2) a second catalyst component comprising at least one member selected from the group consisting of lanthanide group metals and compounds thereof; andcollecting the resultant carbonic acid diester from a reaction mixture discharged from the catalytic reaction step.

Abstract: Organic carbonates and cyclic organic carbonates are prepared by reacting an aliphatic or cycloaliphatic alcohol, or, respectively, an aliphatic diol, with carbon monoxide and oxygen, by operating in the presence of a complex catalyst of cobalt with organic ligands bearing one or more oxygen functional groups, as electron donors.

Abstract: A process for producing dialkyl carbonates which comprises contacting an alkanol, carbon monoxide, and oxygen with a catalyst to produce dialkyl carbonate, the catalyst having been prepared by heating a solid copper compound in the presence of a zeolite to form a zeolite containing copper.

Abstract: Describes a process for preparing N,O-disubstituted hydroxylamine compounds comprising reacting an aqueous solution of free hydroxylamine with an equimolar amount of a carbonyl halide-containing compound, e.g., a chloroformate such as phenyl chloroformate, in the presence of a substantially stoichiometric amount of a weak inorganic basic reagent, thereby to produce the N-substituted derivative, and thereafter further reacting an inert organic solvent solution of the N-substituted derivative with an equimolar amount of the corresponding carbonyl halide-containing compound in the presence of a substantially stoichiometric amount of weak inorganic basic reagent, thereby to produce the N,O-disubstituted derivative, e.g., N,O-bis(phenoxycarbonyl) hydroxylamine. In a preferred embodiment, the organic solvent is used also in the reaction that produces the N-substituted derivative. N,O-disubstituted hydroxylamine compounds containing less than 3 weight percent, e.g., less than 0.

Abstract: The invention relates to a novel process for the preparation of compounds of formula I ##STR1## wherein R is straight-chain C.sub.2 -C.sub.4 alk-1-en-1-yl, and salts thereof, and to a novel starting material and the use thereof.

Abstract: Carbonic diesters containing at least one aromatic ester group can be prepared from carbonic diesters containing at least one aliphatic ester group by transesterification using a phenol, titanium dioxide having a surface area of at least 20 m.sup.2 /g as determined by the BET method being used as catalyst.

Abstract: A process for producing alkylene carbonates which comprises reacting urea and glycols described by the general formula RCH(OH) CH.sub.2 OH; wherein R represents hydrogen or an alkyl group containing 1 to 4 carbons, using a catalyst containing zinc, magnesium, lead or calcium at reduced pressures. The alkylene carbonates are produced with high yield easily using raw materials which are comparatively inexpensive with a mild reaction that does not involve explosive or hazardous materials.

Abstract: The present invention relates to a novel catalyst having a stable catalytic activity for catalyzing the reaction of an alcohol with carbon monoxide and oxygen to produce carbonic acid esters (i.e., carbonate), and also the present invention relates to a method of producing carbonic acid esters using this catalyst. The catalyst of the present invention comprises a copper halide and at least one hydroxide compound selected from a group consisting of alkali metal hydroxides and alkali earth metal hydroxides carried on a porous carrier, and also provide a process of regenerating a catalytic activity of the catalyst.

Abstract: This invention is directed to novel allyl carbonates and to solid electrolytes containing a solid matrix having incorporated therein allyl carbonates. The solid matrix is used in an electrolytic cell.

Abstract: A method is provided for depolymerizing scrap aromatic polycarbonate to salvage component monomers by initially effecting aromatic polycarbonate depolymerization by basic phenolysis to produce a mixture having dihydric phenol, and diarylcarbonate. Recovery of the dihydric phenol is effected by distillation of a crystalline dihydric phenol/phenol adduct. Diarylcarbonate is recovered by distillation of the resulting mother liquor after carboxylic acid treatment.

Abstract: In a process for the stabilization of a solution of ethylmagnesium carbonate in ethanol, which has been prepared by the reaction of a suspension of magnesium ethylate in ethanol with carbon dioxide, 0.2 to 1.0% by weight of water, based on the ethylmagnesium carbonate solution, is added to the solution or its starting materials.

Abstract: Dialkyl carbonates can be prepared by the reaction of carbon monoxide with alkyl nitrites in a continuous gas phase reaction, using a platinum metal catalyst on an amorphous alumosilicate having a content of 30-80 atom% Al, based on the sum of Al and Si, as a support, which catalyst may optionally comprise additional material of a compound of antimony, bismuth, aluminium, copper, vanadium, niobium, tantalum, tin, iron, cobalt, nickel or a mixture of a plurality of these, and hydrogen halide being added in the course of the reaction intermittently or continuously. In this reaction, the dialkyl carbonates are formed with almost quantitative selectivity; the corresponding dialkyl oxalates cannot be detected in most cases.

Abstract: The present invention relates to a novel and efficient process for the preparation of 8-hydroxybicyclo[7.3.1]tridec-4-ene-2,6-diyne ring system which is part of the aglycone of esperemicin and to novel cytotoxic antitumor agents having said bicyclic ring system. The present invention also provides a method for treating mammalian malignant tumors by administering to an animal in need of such treatment an antitumor effective amount of a compound of the present invention.