Patents - stay tuned to the technology

Inventors list

Assignees list

Classification tree browser

Top 100 Inventors

Top 100 Assignees


PHOSPHORUS CONTAINING

Subclass of:

568 - Organic compounds -- part of the class 532-570 series

568000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

Patent class list (only not empty are listed)

Deeper subclasses:

Class / Patent application numberDescriptionNumber of patent applications / Date published
568008000 PHOSPHORUS CONTAINING 71
20090054690Process for producing biarylphosphine compound - A process for producing a biarylphosphine compound is disclosed. The process has a step of subjecting a biarylsulfonate compound to coupling reaction with a hydrogen-phosphine compound in the presence of a catalyst and an organic strong base to obtain a biarylphosphine compound. As the catalyst, preferably used is a nickel compound or a palladium compound. As the organic strong base, preferably used is 1,8-diazabicyclo[5.4.0]undecene-7 (DBU).02-26-2009
20120220803Process for Production of Trialkylphosphine - A production process of a trialkylphosphine according to the present invention includes: a first step of forming a trialkylphosphine by reaction of an organic metal compound and an organic phosphorous compound in an ether solvent having a difference in boiling point with the trialkylphosphine formed such that the difference in boiling point is in a range of 0° C. to 20° C.; a second step of obtaining a silver complex by absorption of a gas phase of the first step into an aqueous solution of AgI and KI; a third step of heating the silver complex obtained in the second step, in a metallic reaction vessel, at a temperature of 170° C. to 350° C. in a reduced pressure atmosphere of 1.333×1008-30-2012
568009000 Phosphonium derivative 14
20080255391Chiral Phosphorus Compounds - A process for the stereoselective preparation of a P-chiral four-co-ordinated phosphorus compound, the process comprising reacting a first reactant selected from the group consisting of a chiral alcohol, chiral amine or chiral thiol, with a second reactant comprising a P-chiral three-co-ordinated phosphorus compound, in the presence of an electrophile.10-16-2008
20110021838PHOSPHONIUM SALTS AND METHODS OF THEIR PREPARATION - Methods for preparing phosphonium salts by reacting a primary phosphine or a secondary phosphine with an ester compound selected from the group consisting of: a phosphate triester; a phosphonate diester; a sulfate diester; and a sulfonate ester; to form a phosphonium salt of formula VII01-27-2011
20140051889ISOMERIZATION OF OLEFINIC COMPOUNDS - The present invention relates to a process for preparing an olefinically unsaturated phosphonium salt having at least two olefinic double bonds, of which one double bond has a Z or cis conformation and the second or a further double bond an E conformation, from an olefinically unsaturated phosphonium salt having at least two olefinic double bonds of different configuration compared to the target compound, and both especially have an all-E or all-trans conformation. In addition, the invention provides for the use of the compound obtained by the process for provision of terpenoid substances as medicaments.02-20-2014
20140378709PREPARATION METHOD OF 3,7,11- TRIMETHYLDODEC -2,4,6,10-TETRAENE-1-YL-PHOSPHONIC SALT - Provided in the present invention is a preparation method for a phosphonic salt, comprising the step of: reacting 3,7,11-trimethyldodec-1,4,6,10-tetraene-3-ol with triarylphosphine and an acid in an alcohol solvent at 50-100° C. to form the phosphonic salt, wherein the acid is a sulfamic acid or methanesulfonic acid, and the alcohol solvent is a straight chain monohydric alcohol containing 1-5 carbon atoms. The method is performed in nearly neutral conditions, greatly reducing the generation of impurities and greatly obtaining phosphonic salt with an increased E content. The yield of lycopene obtained by using the phosphonic salt as a raw material is high.12-25-2014
20160009611METHODS FOR PREPARATION OF LYCOPENES FROM C15-WITTIG SALTS AND METHODS FOR PURIFICATION OF HIGH ALL-E CONTAINING AND HIGH 6Z CONTAINING C15-WITTIG SALTS01-14-2016
20160167034HYDROCHLORIC ACID STRIPPING PROCESS FOR IONIC LIQUID REGENERATION PROCESS06-16-2016
568010000 Plural phosphori containing 2
20080221362Optically-active bis(alkynylphosphino) ethane-borane derivative and process for producing the same - An optically-active bis(alkynylphosphino)ethane-borane derivative represented by formula (1):09-11-2008
20110015440PHOSPHINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND PEROXIDE SCAVENGER USING THE SAME - The invention provides a novel peroxide scavenger comprising a phosphine compound represented by general formula [I]:01-20-2011
568011000 Sulfur or oxygen containing 6
20080269526METHODS OF MAKING AN ANTISTATIC AGENT - Disclosed are methods for making the phosphonium sulfonate salt of generic formula (1):10-30-2008
20100197969USE OF PHOSPHONIUM SALTS IN COUPLING REACTIONS AND PROCESS FOR THEIR MANUFACTURE - The object of the present invention is the use of phosphonium salts in coupling reactions, and a method for their preparation.08-05-2010
20110160487ITQ-40, New Crystalline Microporous Material - ITQ-40 (INSTITUTO DE TECNOLOGÍA QUÍMICA number 40) is a new crystalline microporous material with a framework of tetrahedral atoms connected by atoms capable of bridging the tetrahedral atoms, the tetrahedral atom framework being defined by the interconnections between the tetrahedrally coordinated atoms in its framework. ITQ-40 can be prepared in silicate compositions with an organic structure directing agent. It has a unique X-ray diffraction pattern, which identifies it as a new material.06-30-2011
20110224461MODIFIED ION EXCHANGE RESIN AND PROCESS FOR PRODUCING BISPHENOLS - There is provided a modified ion exchange resin catalyst which exhibits higher bisphenols selectivity than the conventional modified ion exchange resins in processes wherein bisphenols are produced by reacting a phenolic compound with ketones, and to provide such a process for producing bisphenols. A modified ion exchange resin is characterized in that at least one compound selected from (A) and (B) shown below is ionically bonded to an acidic functional group of an acidic ion exchange resin: 09-15-2011
20130116473PROCESS FOR THE PREPARATION OF OXOVINYLIONOL AND ITS O-PROTECTED DERIVATIVES - The present invention relates to the preparation of oxovinylionol and its O-protected derivatives of the formula I05-09-2013
20150087863CURING COMPOSITION FOR FLUOROPOLYMERS - Provided is a catalyst composition suitable for curing a fluoroelastomer, the catalyst composition comprising an anion of Formula III:03-26-2015
568012000 Ring phosphorus containing 19
20080262269Monodonor Phosphonite Ligands - The invention provides the use of a metal complex, which is a complex of one or more metal atoms or ions with one or more ligands, as a catalyst in an organic transformation selected from hydrogenation of carbon-heteroatom double bonds, hydroformylation, dialkylzinc additions to aldehydes, hydrocarboxylation, allylic substitution, oxidation, epoxidation, dihydroxylation, Diels-Alder cycloadditions, dipolar cycloadditions and rearrangement reactions, wherein one or more of the ligands is a ligand of formula (1), wherein the bridge group is an organic functional group, and the R group is a substituted phenyl group, wherein the R group has only one substituent at the ortho position, and wherein a carbon atom of the R group bonds the R group to the P atom. Also provided are monodonor ligands of formula (1) wherein the bridge group is an unsubstituted or substituted binaphthyl group and the R group is a substituted phenyl group, wherein the substituents are selected from halogen, nitro, alkynyl and sulfonic acid groups and unsubstituted or substituted alkyl, aryl, amino and vinyl groups, and wherein the R group has only one substituent at the ortho position, and wherein a carbon atom of the R group bonds the R group to the P atom.10-23-2008
20080287713Halophospholanes And Their Preparation - The present invention is directed to a process for preparing compounds of the general formula (I). Compounds of the general formula (I) are advantageous precursors for preparing phospholane catalysts, especially bisphospholane catalysts. The invention therefore likewise provides for the use of the substances in question for preparing these catalysts.11-20-2008
20090171120PHOSPHORUS-BASED OXAZINE COMPOUNDS AND PREPARATION METHOD OF THE SAME - The present invention provides phosphorus-based oxazine compounds and the preparation method thereof. The phosphorus-based oxazine compounds of the present invention can provide better fire-resistant characteristics, while the preparation method for the phosphorus-based oxazine compound of the present invention can offer high yields and/or high purity phosphorus-based oxazine compounds.07-02-2009
20090171121FLUOROPHOSPHITE CONTAINING CATALYSTS FOR HYDROFORMYLATION PROCESSES - Novel fluorophosphite compounds having the structure of general formula (I):07-02-2009
20090171122PHOSPHONITE CONTAINING CATALYSTS FOR HYDROFORMYLATION PROCESSES - Novel trivalent organophosphonite ligands having the structure of general formula (I):07-02-2009
20090247790ISOTHERMAL PROCESS FOR PHOSPHOROMONOCHLORIDITE SYNTHESIS - The present invention relates to a process for preparation of a phosphoromonochloridite in high yield by contacting phosphorus trichloride (PCl10-01-2009
20090259073METHOD FOR PRODUCING ALDEHYDE USING BISPHOSPHITE AND GROUP 8-10 METAL COMPOUND, AND SUCH BISPHOSPHITE - A bisphosphite represented by the general formula (I): 10-15-2009
20090299099HYDROFORMYLATION CATALYSTS - This invention is directed to a class of compounds that can be both monodentate and bidentate in their association with a transition metal to form a catalyst for reactions such as the hydroformylation of olefins to produce aldehydes. The compounds contain two phosphorus atoms having different steric and/or electronic nature. In hydroformylation catalysts, the compounds advantageously can produce a variable n/iso product mixture of aldehyde products that can be varied by simply changing process variables such as [H12-03-2009
20100036171LIGAND, CATALYST AND PROCESS FOR HYDROFORMYLATION - According to the present invention, there is provided an organophosphine ligand comprising a phosphabicyclohydrocarbyl group in which the phosphorus atom is further substituted with a hydrocarbyl or heterohydrocarbyl moiety containing at least one branch at the β-carbon position. The present invention also provides a catalytic composition for the hydroformylation of an ethylenically unsaturated compound, said catalytic composition comprising i) a source of Group VIII metal cations; and ii) the above ligand. Furthermore, the present invention also provides a process for the hydroformylation of an ethylenically unsaturated compound, said process comprising contacting the ethylenically unsaturated compound with carbon monoxide and hydrogen in the presence the above catalytic composition.02-11-2010
20100125154PHOSPHORUS COMPOUND AND METHOD FOR PREPARING THE SAME - The present invention provides a phosphorus compound of formula (I).05-20-2010
20110021839PHASE TRANSFER CATALYST FOR SYNTHESIS OF PENTAERYTHRITOL DIPHOSPHITES - The present invention pertains to a process for the preparation of pentaerythritol diphosphites via a one-pot, direct esterification of phosphorus trichloride with pentaerithritol, and either an alkylphenol or an arylalkylphenol which functions both as a reactant and as a solvent, with a phase transfer catalyst such as a quaternary ammonium salt.01-27-2011
20110021840SLURRY PROCESS FOR PHOSPHOROMONOCHLORIDITE SYTHESIS - A process for preparation of a phosphoromonochloridite in high yield, by contacting phosphorus trichloride (PCl01-27-2011
20110207966METHOD FOR PRODUCING 6-CHLORODIBENZO[D,F] [1,3,2]-DIOXAPHOSPHEPIN - The invention relates to a method for producing 6-chlorodibenzo[d,f][1,3,2]dioxaphosphepin (formula 1), comprising the following steps: a) addition of 2,2′-dihydroxybiphenyl, which is suspended in an inert solvant. into a reactor to an excess of phosphorous trichloride under inert gas and stirring; b) discharge and neutralization of the resulting gases from the reaction mixture; c) separation of the excess phosphorous trichloride and the solvant; d) obtention of 6-chlorodibenzo[d,f][1,3,2]dioxaphosphepin.08-25-2011
20130137902Monophosphorus Ligands And Their Use In Cross-Coupling Reactions - Phosphine ligands of the formula Ia, IB and mixtures thereof.05-30-2013
20140206904METHOD FOR PRODUCING 6-CHLORODIBENZO[D,F] [1,3,2] DIOXAPHOSPHEPIN - The invention relates to a method for producing 6-chlorodibenzo[d,f] [1,3,2]-dioxaphosphepin (formula 1), comprising the following steps: a) addition of 2,2′-dihydroxybiphenyl, which is suspended in an inert solvant. into a reactor to an excess of phosphorous trichloride under inert gas and stirring; b) discharge and neutralization of the resulting gases from the reaction mixture; c) separation of the excess phosphorous trichloride and the solvant; d) obtention of 6-chlorodibenzo[d,f] [1,3,2]-dioxaphosphepin.07-24-2014
20140275628Large scale preparation method for functionalizing the surface of magnetic microparticles with an inorganic phosphorous dendrimer - A method of attaching a phosphorous dendrimer onto magnetic microparticles by taking magnetic microparticles in a water-based solution, then performing a solvent exchange, then suspending the microparticles in a phosphorous dendrimer solution and shaking, then washing the microparticles with an organic solvent, and then washing the microparticles with a transition solvent. The solvent exchange is done by washing the microparticles with a first concentration of a transition solvent, then washing the microparticles with a second concentration of the transition solvent where the second concentration is greater than the first concentration, then washing the microparticles with an organic solvent, then washing the microparticles with the transition solvent, then washing the microparticles with the organic solvent, and then suspending the microparticles in the transition solvent. Also disclosed is the related phosphorous dendrimer made by this method.09-18-2014
20150376215Method Of Producing Phospholene Oxide - A method of producing a phospholene oxide is disclosed. A dihalohydrocarbylphosphine, 2-methyl-1,3-butadiene, and a halogenated hydrocarbon solvent are combined to form an adduct via an addition reaction in a homogenous system wherein the ratio of the 2-methyl-1,3-butadiene to the dihalohydrocarbylphosphine is from 1.0 to 2.0 and wherein the solvent is present in an amount of greater than 200 mL per mole of dihalohydrocarbylphosphine. The adduct is combined with alcohol and a carbonate or with a solution of metal hydroxide and water to form the phospholene oxide.12-31-2015
20160159835BISPHOSPHITES HAVING AN OUTER NAPHTHYL-PHENYL UNIT - Bisphosphites having an outer naphthyl-phenyl unit.06-09-2016
20160159836BISPHOSPHITES HAVING AN OUTER NAPHTHYL-PHENYL UNIT AND A CENTRAL 2,3'-BIPHENOL UNIT - Bisphosphites having an outer naphthyl-phenyl unit and a central 2,3′-biphenol unit and their preparation are described.06-09-2016
568013000 Sulfur or oxygen containing 30
20080221363Process for the Monosulfonation of Aromatic Phosphines, and Zwitterionic Product Derived Therefrom - A method of preparing an aromatic phosphine monosulfonate in zwitterionic form, such as dicyclohexylphenylphosphine monosulfonate zwitterion, involving contacting an aromatic phosphine with a sulfonating agent to provide a reaction mixture containing aromatic phosphine monosulfonate in acid form and unconverted sulfonating agent; quenching or removing substantially all of the unconverted sulfonating agent; partially neutralizing the aromatic phosphine monosulfonate in acid form to phase separate aromatic phosphine monosulfonate in zwitterionic form as a solid or neat liquid layer; and collecting the zwitterion as a solid or neat liquid. The zwitterion may be neutralized to form the corresponding aromatic phosphine monosulfonate metal salt, which is useful in preparing catalysts for hydroformylation processes.09-11-2008
20090048467METHODS FOR MAKING IMMOBILIZED ARYL-CONTAINING LIGANDS - Organic ligands that contain at least one aryl group are immobilized on a solid support. The organic ligands are of the type used to form a catalyst complex suitable for carrying out a catalytic reaction, preferably an asymmetric reaction. To immobilize the organic ligands, a tethering group is bonded to the ligand using, for example, a Friedel-Crafts acylation or alkylation reaction. The immobilization of the organic ligand can be carried out using a single reaction with the organic ligand.02-19-2009
20090105505PROCESS FOR THE PREPARATION OF ASYMMETRICALLY SUBSTITUTED BIARYLDIPHOSPHINES - A process for the preparation of asymmetrically substituted biaryldiphosphine ligands of the formula:04-23-2009
20130261342PROCESS FOR TELOMERIZATION OF BUTADIENE USING A MONO-ORTHOALKOXY SUBSTITUTED CATALYST - A process for the telomerization of butadiene comprises reacting 1,3-butadiene and an alkanol, in the presence of a catalyst promoter and an alkoxydimerization catalyst comprising a Group VIII transition metal and a triarylphosphine ligand, which includes one phenyl that is mono-ortho-alkoxy substituted and at least one other phenyl including at least one substituent that withdraws electrons from the phosphorus atom. The product includes an alkoxy-substituted octadiene, which may then be used to produce 1-octene. The catalyst shows improved stability, activity and selectivity toward the alkoxy-substituted octadiene.10-03-2013
20140114090LIGANDS AND CATALYST SYSTEMS FOR HYDROFORMYLATION PROCESSES - The present invention relates to ligands and catalyst systems for the hydroformylation of short and long chain olefins, preferably for the hydroformylation of ally alcohol producing 4-hydroxybutyraldehyde. The ligands disclosed herein are all-trans phosphinomethyl-cyclobutane ligands, such as, for example, all-trans-1,2,3, 4-tetra[bis-(3,5-xylyl)phosphinomethyl]-cyclobutane. The catalyst systems comprise these all-trans phosphinomethyl-cyclobutane ligands in combination with an organometallic rhodium complex such as, e.g., (acctylacetonato)-dicarbonyl-rhodium (I). The ligands and catalyst systems of the present invention may be employed in the hydroformylation of olefins, in particular in the hydroformylation of allylalcohol, and provide improved selectivity and high reaction yields. wherein R04-24-2014
20160052947BIS(6-METHYL-3-SULPHOPHENYL)PHENYLPHOSPHINE, AMMONIUM SALT THEREOF, AND METHOD FOR PRODUCING SAME - Provided are a water-soluble triarylphosphine for a palladium catalyst, which has high selectivity in a telomerization reaction and can be recovered with efficiency, an ammonium salt thereof, and a method for efficiently producing the same. Specifically, provided are bis(6-methyl-3-sulphophenyl)phenylphosphine; a bis(6-methyl-3-sulphonatophenyl)phenylphosphine diammonium salt obtained by reacting the phosphine with a tertiary amine having a total of 3 to 27 carbon atoms in groups bonded to one nitrogen atom; and a method for producing the same.02-25-2016
568014000 Sulfur or oxygen bonded directly to phosphorus 24
20080234519Process For the Manufacture of Aminopolyalkylenephosphonic Acid Compounds - A beneficial method for the manufacture of amino polyalkylene phosphonic acids, under substantial absence of hydrohalogenic acid, is disclosed. The method, in essence, is based on reacting narrowly defined ratios of phosphorous acid, an amino, a formaldehyde in presence of specific ranges of an acid catalyst having a pKa equal or inferior to 3.1. The inventive method is capable of yielding economically and quality operational/capacity advantages, in particular significantly reduced one-step cycle duration under exclusion, of corrosion disadvantages and also is environmentally friendly without requiring, in that respect, anything more than nominal capital expenditures.09-25-2008
20080242893Process for Preparing Optically Active Diphosphanes - The present invention relates to a process for preparing optically active bisphosphinylalkanes from the correspondingly substituted, racemic 1,2-diols. The optically active bisphosphinylalkanes which can be obtained in this way are suitable as ligands for preparing chiral transition metal catalysts.10-02-2008
20080275273Method for Synthesizing Long-Chain Phosphonic Acid Derivatives and Thiol Derivatives - A process for synthesizing long-chain phosphonic acid derivatives and thiol derivative is disclosed. One embodiment provides organic compounds which can form a self-assembled monolayer and are obtained by reaction of an olefin with a thiocarboxylic acid and subsequent hydrogenation to give the thiol, or with a phosphite and subsequent hydrolysis to give the phosphonic acid.11-06-2008
20090203942DIARYL ALKYLPHOSPHONATES AND METHODS FOR PREPARING SAME - A method for preparing substantially pure optionally substituted diaryl alkylphosphonates from an optionally substituted triarylphosphite and an optionally substituted trialkylphosphite or an optionally substituted alkanol under special reaction conditions is described.08-13-2009
20090275782Quantum Dots Tailored with Electronically-Active Polymers - Cadmium selenide, and other quantum dot materials, can be integrated into thin films of poly(para-phenylene vinylene) (PPV) or other polymer compounds without aggregation of the nanocrystals. Solid-state photoluminescence spectra of composite materials prepared by these novel techniques reveal the effect of this greatly enhanced quantum dot-polymer interface relative to cases where the nanoparticles are aggregated, such that electronic communication and energy transfer between the nanoparticle and polymer components is made more efficient.11-05-2009
20090281356METHOD FOR PRODUCING ORGANIC PHOSPHOROUS COMPOUNDS CONTAINING HALOGENE - Method of producing compounds of the general formula11-12-2009
20100137643METHOD FOR SYNTHESIZING CYCLOHEXYL-SUBSTITUTED PHOSPHINES - The present invention relates to a process for preparing cyclohexyl-substituted phosphines. The invention further relates to a process for preparing cyclohexyl-substituted phosphine oxides which can be used as intermediates in the preparation of cyclohexyl-substituted phosphines.06-03-2010
20100267990HIGHLY SELECTIVE PROCESS FOR PRODUCING ORGANODIPHOSPHITES - Disclosed is a method for making a diphosphite of Structure I,10-21-2010
20100267991HIGHLY SELECTIVE PROCESS FOR PRODUCING ORGANODIPHOSPHITES - Disclosed is a method for making a diphosphite of Structure I,10-21-2010
20100324337PROCESS FOR PRODUCING HIGH-PURITY CHLOROPHOSPHITE - There is provided a process capable of preventing the adhesion of a catalyst to an evaporator in a step of separating a chlorophosphite as a target substance from a reaction liquid by evaporation. The process includes a first step of allowing phosphorus trichloride and a phosphorous acid triester represented by (RO)12-23-2010
20110034734UNSATURATED DIPHOSPHINE MONOXIDES - The present invention relates to unsaturated diphosphine monoxides, to a process for preparation thereof and to the use thereof as flame retardants.02-10-2011
20110098507Asphalt Dispersers On The Basis Of Phosphonic Acids - The object of the invention is the use of phosphonic acids of the formula (4),04-28-2011
20110124921METHOD FOR PRODUCING BIS(FLUORALKYL)PHOSPHINIC ACID CHLORIDES OR FLUORALKYLPHOSPHONIC ACID CHLORIDES - The invention relates to a process for the preparation of bis(fluoroalkyl)phosphinyl chlorides or fluoroalkylphosphonyl dichlorides by reaction of the corresponding bis(fluoroalkyl)phosphinic acid or fluoroalkylphosphonic acid with aryltetrachlorophosphorane as chlorinating agent05-26-2011
20120108849POLYFLUOROALKYLPHOSPHONIC ACID ESTER AND PROCESS FOR PRODUCING THE SAME - A polyfluoroalkylphosphonic acid ester represented by the general formula: C05-03-2012
20120330063PROCESS FOR THE PREPARATION OF TRIS(PERFLUOROALKYL)PHOSPHINE OXIDES - The invention relates to a process for the preparation of tris(perfluoroalkyl)phosphine oxides by reaction of tris(perfluoroalkyl)difluorophosphorane with alkaline-earth metal oxides, alkaline-earth metal carbonates, zinc oxide, copper(I) oxide, copper(II) oxide, silver oxide, mercury(II) oxide, cadmium oxide or cadmium carbonate12-27-2012
20150141698PROCESS FOR THE PREPARATION OF TRIS(PERFLUOROALKYL)PHOSPHINE OXIDES AND BIS(PERFLUOROALKYL)PHOSPHINIC ACIDS - The invention relates to a method for producing tris(perfluoroalkyl)phosphine oxides and bis(perfluoroalkyl)phosphinic acids by reacting tris(perfluoroalkyl)difluorophosphorane or bis(perfluoroalkyl)trifluorophosphorane with non-metal oxides, metalloid oxides or organic compounds with basic oxygen residues.05-21-2015
568015000 And sulfur or oxygen bonded indirectly to phosphorus 8
20080300427PROCESS FOR PRODUCING PHOSPHINE OXIDE VITAMIN D PRECURSORS - A process for producing a compound of the formula:12-04-2008
20080319231Process for the Preparation of Alkyl Phosphinates - The invention relates to a new process for the production of alkyl dialkoxyalkylphosphinates. A hypophosphite salt is used in the process.12-25-2008
20090062568PROCESS FOR PREPARING PHOSPHONATES HAVING ALCOHOLIC HYDROXYL GROUP - A novel process for preparing in a high purity and in a high yield phosphonates having a secondary and/or tertiary alcoholic hydroxyl group at the end of a P—C bond chain thereof with the use of a phosphite and a carbonyl compound as raw materials.03-05-2009
20100152491PROCESSES FOR PREPARING (E)-STYRYLBENZYLSULFONE COMPOUNDS AND USES THEREOF FOR TREATING PROLIFERATIVE DISORDERS - Processes for preparing (E)-2,4,6-(Trimethoxystyryl)-3-O-Phosphate Disodium-4-Methoxybenzyl Sulfones and uses thereof as antiproliferative agents, including, for example, anticancer agents, and as radioprotective and chemoprotective agents.06-17-2010
20130310606METHOD FOR PRODUCING POLYPRENYL PHOSPHATES - Method produces polyprenyl phosphates of formula,11-21-2013
20140135530NOVEL COMPOUND AND ORGANIC DEVICE EMPLOYING SAME - The compounds represented by the following general formula have excellent properties as a charge transport material. In the formula, R05-15-2014
20150018579SYNTHESIS OF HIGH PURITY DMT-C3-DISULFIDE PHOSPHORAMIDITE - The 5′ and 3′-thiol modified oligonucleotides are attractive tools with a vast number of potential applications in the field of nucleic acid chemistry. There is a strong interest in developing new disulfide compounds or to optimize synthesis of existing disulfide modifiers, which are efficient in generating the 3′- or 5′-end reactive thiol group. Various synthetic protocols have been employed to synthesize pure 3-((3-(bis(4-dimethoxytrityl)propyl)di-sulfanyl)propyl 2-cyanoethyl diisopropylphosphoramidite (compound 2) starting from 3-(dimethoxytrityl)propyl)disulfanyl)pro-pan-1-ol, (compound 1). Herein, we describe an efficient, reproducible synthetic and purification protocol for target compound 2 from the compound 1. It is noteworthy that our reaction conditions were reproducible even at multi-gram scale (27 g) with a purity level as achieved in a small scale.01-15-2015
20150361117PREPARATION OF A HYDROXYALKYL PHOSPHONIC ACID - The present invention is a process for converting a phosphonate to a hydroxyalkyl phosphonic acid comprising the step of contacting together water, the phosphonate, and a sulfonated or phosphonated heterogeneous catalyst under conditions sufficient to convert at least 50% of the phosphonate to the hydroxyalkyl phosphonic acid. The process of the present invention provides a way of preparing hydroxyalkyl phosphonic acids safely and economically, without corrosive effects.12-17-2015
568016000 Halogen containing 1
20110071319METHOD FOR PREPARING HALOGENATED ORGANOPHOSPHINES - The present application relates to a process for preparing a halogenated organophosphine, comprising reacting a primary or secondary organophosphine with a halogenating agent selected from (A) a compound of formula (I): (HaI)03-24-2011
568017000 Benzene ring containing 5
20080200729Preparation of Aryl Phosphines - A method of making an aryl phosphine is provided. The method comprises reacting an organophosphine of general formula (1): HPXY with a substituted aryl compound in the presence of a catalyst, a base, a ligand and an iodine containing co-catalyst. In formula (1) X and Y can be the same or different and are cycloalkyl; substituted alkyl; primary, secondary and tertiary alkyl; and heterocyclic moieties; and one of X and Y can optionally be hydrogen.08-21-2008
20100197970METHOD FOR PRODUCING NORBORNENE DERIVATIVE - A method for producing a norbornene derivative wherein, 08-05-2010
20100234642NAPHTHENIC HYDROCARBON ADDITIVES FOR DIARYL PHOSPHIDE SALT FORMATION - The invention relates to the use of polycyclic aromatic hydrocarbons (PAHs) such as naphthalene and its alkyl, aryl, or heteroatom substituted analogs, that act as catalysts in the presence of an alkali metal (Li, K, Na) for the reduction of electron-deficient and electron-rich triaryl phosphines to their corresponding alkali metal diaryl phosphide salts. The process is also useful for the catalysis of triaryl phosphine chalcogen adducts such as the sulfides, oxides, and selenides, diaryl(halo)phosphines, triaryl phosphine-borane adducts, and tetra-aryl bis(phosphines) that can also be reduced to their corresponding alkali metal diaryl phosphide salts. The invention also relates to small molecule PAHs and polymer tethered PAHs naphthenics.09-16-2010
20110065961PROCESS FOR PRODUCTION OF PHOSPHINE DERIVATIVE FROM PHOSPHINE OXIDE DERIVATIVE - Disclosed is a process for producing a phosphine derivative from a phosphine oxide derivative, which comprises the following steps: (I) mixing a phosphine oxide derivative represented by formula (1) with a chlorinating agent in a polar organic solvent to cause the reaction between these components; and (II-1) adding a salt of a metal having an ionization tendency equal to or lower than that of aluminum to the reaction mixture and carrying out the reductive reaction in the presence of aluminum or (II-2) subjecting the reaction mixture to electrolytic reduction, thereby producing a phosphine derivative represented by formula (2). Ar03-17-2011
20160095869COMPOUNDS AS MODULATORS OF A MUTANT CFTR PROTEIN AND THEIR USE FOR TREATING DISEASES ASSOCIATED WITH CFTR PROTEIN MALFUNCTION - An exemplary embodiment relates to novel protein modulators capable of altering function of the mutant CFTR protein and their use for treating diseases associated with CFTR protein malfunction. An exemplary embodiment provides compositions, pharmaceutical preparations and methods of correcting the cellular alteration of a mutant CFTR protein wherein the CFTR mutation is a mutation ΔF508-CFTR, or another mutation of class II.04-07-2016

Patent applications in all subclasses PHOSPHORUS CONTAINING

Website © 2025 Advameg, Inc.