Abstract: The invention concerns compounds of formula (1) wherein in particular G represents the —N(CH3)2—, —N(C2H5)2-group or N-pyrrolidine: n is an integer equal to 1 or 2: R1, R2 and R3, independently of one another, represent a hydrogen atom or a methyl group, the successive unsaturated units capable of being moreover identical or different, provided that at least one of the substituents R1, R2 and R3 is different from H: and Y1 and Y2 represent each a —COOCH3 group or a COOC2H5 group.

Abstract: A process for rectificatively separating a liquid which comprises acrylic acid, methacrylic acid or a mixture thereof, and additionally comprises low molecular weight aldehydes and acetone.

Abstract: Therapeutic compounds, methods, and compositions are disclosed herein. These compounds have prostaglandin EP2 activity, and are useful to treat and/or prevent glaucoma and/or ocular hypertension in a mammal.

Abstract: The invention aims at producing high-purity crystals of a hydroxycarboxylic acid represented by the following formula (1): in high yield. Provided are a method for crystallization of a compound (1) which comprises acidifying a mixture of a solution of an alkali salt of the compound (1) and an organic solvent, and a method for crystallization of compound (1) by mixing a solution of the compound (1) in a water-miscible good solvent with water, in which a slurry with a necessary suspension amount of the compound (1) for inhibiting oil formation and scaling is prepared in advance and then a main crystallization is carried out in the presence of said slurry.

Abstract: A process for preparing acid formates which comprises (a) partially hydrolyzing methyl formates with water; (b) separating off by distillation methyl formate and methanol from the reaction mixture obtained in process stage (a), forming a stream comprising formic acid and water; and (c) combining the stream comprising formic acid and water from the process stage (b) and the corresponding formate, forming a mixture comprising the acid formate and water, an apparatus for their preparation and their use.

Abstract: Disclosed are compounds capable of facilitating transport of biologically active agents or substances into cells having the general structure: wherein Q is selected from the group consisting of N, O and S; L is any bivalent organic radical capable of linking each Q, such as C, CH, (CH2)l, or {(CH2)i-Y—(CH2)j}k, wherein Y is selected from the group consisting of CH2, an ether, a polyether, an amide, a polyamide, an ester, a sulfide, a urea, a thiourea, a guanidyl, a carbamoyl, a carbonate, a phosphate, a sulfate, a sulfoxide, an imine, a carbonyl, and a secondary amino group and wherein Y is optionally substituted by -X1-L?-X2-Z or -Z; R1-R6, independently of one another, are selected from the group consisting of H, —(CH2)p-D-Z, an alkyl, an alkenyl, an aryl, and an alkyl or alkyl ether optionally substituted by one or more of an alcohol, an aminoalcohol, an amine, an amide, an ether, a polyether, a polyamide, an ester, a mercaptan, an alkylthio, a urea, a thiourea, a guanidyl, or a carbamoyl group, and

Abstract: A compound having the formula wherein R1, Z, and the carbonyl can be comprised by a common ring, wherein R1 comprises a chromophore that absorbs light from the visible wavelength range, and wherein n is an integer of at least 12. A solid phase change ink composition is also disclosed containing a colorant comprising a chromophore that absorbs light from the visible wavelength range and has the formula wherein R1, Z, and the carbonyl can be comprised by a common ring, and wherein n is an integer of at least 12. Also disclosed is a method of forming a colorant wherein a first compound having the formula is reacted with a second compound having the formula Z(CH2)nCH3 wherein n is an integer of at least 12 to form a third compound having the formula wherein the third compound comprises a chromophore that absorbs light from the visible wavelength range.

Abstract: Compounds of formula (I) and (IA) have antibacterial or antiprotozoal activity: formula (1) formula (2) wherein: Z represents a radical of formula N(OH)CH(?O) or of formula C(?O)NH(OH); R1 represents hydrogen, methyl or trifluoromethyl, or, except when Z is a radical of formula N(OH)CH(?O), a hydroxy or amino group; R2 represents a radical of formula R10—(X)n-(ALK)m- wherein R10 represents hydrogen, or an optionally substituted c1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, cycloalkyl, aryl, or heterocyclyl group, ALK represents a straight or branched divalent C1-C6 alkylene, C2-C6 ?alkenylene, or C2-C6 alkynylene radical, and may be interrupted by one or more non-adjacent NH—, —O— or S— linkages, X represents NH—, —O— or S—, and m and n are independently 0 or 1; R3 represents hydrogen, C1-C6alkyl, or benzyl; and R4 is as defined in the specification.

Abstract: A process for preparing xylylenediamine by continuously hydrogenating liquid phthalonitrile over a heterogeneous catalyst in the presence of liquid ammonia in a reactor, in which a portion of the reactor effluent is recycled as a liquid circulation stream continuously to the reactor inlet (circulation mode), in which a stream of a phthalonitrile melt in liquid form is conducted by means of a mixer unit into the circulation stream around the hydrogenation reactor, the phthalonitrile conversion in the reactor on single pass being greater than 99%, and the circulation stream consisting to an extent of greater than 93% by weight of liquid ammonia and xylylenediamine and not comprising any further solvent for phthalonitrile.

Abstract: A process for preparing xylylenediamine, comprising the steps of ammoxidizing xylene to phthalonitrile by contacting the vaporous product of this ammoxidation stage directly with a liquid organic solvent (quench), removing products having a boiling point higher than phthalonitrile (high boilers) from the resulting quench solution or suspension and hydrogenating the phthalonitrile, wherein the organic solvent used for the quench is N-methyl-2-pyrrolidone (NMP), after the removal of the high boilers and before the hydrogenation, there is a partial or complete removal of the NMP and/or of products having a boiling point lower than phthalonitrile (low boilers) and the phthalonitrile for the hydrogenation step is dissolved or suspended in an organic solvent or in liquid ammon.

Abstract: A process for preparing amines of the general formula (I) R1R2CHNR3R4??(I) in which R1, R2, R3 and R4 are each independently hydrogen, straight-chain or branched, halogenated or halogen-free C1-C12-alkyl, C3-C12-cycloalkyl, C6-C10-aryl or C7-C11-aralkyl, by catalytic, hydrogenating amination of carbonyl compounds of the general formula (II) R1—C(?O)—R2??(II) with nitrogen compounds of the general formula (III) HNR3R4??(III) in the presence of bifunctional catalyst systems comprising a.) a hydrogenation-active catalyst component comprising one or more metals of transition group 8 of the Periodic Table and b.) one or more solid, acidic cocatalysts, wherein the hydrogenating amination is carried out in the presence of aqueous ammonia or aqueous amine of the formula (III) and at least one organic solvent miscible with ammonia or the aqueous amine of the formula (III).

Abstract: There is provided a regeneration process for converting oxazolidones such as hydroxypropyloxazolidone (HPOZD) to alkanolamines such as di-isopropanolamine (DIPA) and CO2. An amine stream containing HPOZD joins a stream that includes a caustic solution. The combined stream is passed to a tank where the caustic reacts with HPOZD to convert it to DIPA and CO2. The conversion of HPOZD to DIPA and CO2 requires a ratio of at least 2 moles of hydroxide for each mole of HPOZD in the solution. The conversion reaction is carried out in a reaction vessel at a temperature above 60° C. The reaction mixture is held in a feed tank for approximately 2 hours while being constantly mixed. After the reaction is completed, the mixture is allowed to settle which results in the virtually complete separation of the amine phase (containing DIPA, and water) from the caustic phase.

Abstract: Unsaturated alkyllysophosphonocholines compounds of formula (I) or (II): or pharmaceutically-acceptable salts, prodrugs or isomers thereof. The compounds of the invention have anti-neoplastic activity, and accordingly have utility in treating cancer and related diseases. The invention also provides enantiomers of these compounds, as well as synthetic methods for producing an enantiomer, substantially free of the other enantiomer. Also disclosed are pharmaceutical compositions, as well methods for treating cancer with the pharmaceutical compositions.

Abstract: A process for preparing an intermediate compound of formula (II) where n is an integer of from 3 to 14; R1 is haloC1-10alkyl, C1-10alkyl, C2-10alkenyl, C2-10cycloalkyl, carboxyC1-10alkyl, C1-10alkoxycarbonylC1-10alkyl, aryl (such as phenyl), aryl(C1-10)alkyl (such as phenyl(C1-10)alkyl) or di(C1-6alkyl)amino; and R2 is a halo group; the process comprising halogenation of a compound of formula (III) where n and R1 are as defined above. Novel compounds are also described and claimed.

Abstract: A method for aldol reaction in water, which comprises: reacting an aldehyde with a silyl enol ether in an aqueous medium in the presence of a boronic acid represented by the following general formula (1): R1R2BOH??(1) (wherein R1 and R2 are the same or different hydrocarbon groups that may contain a substituent), a surfactant, and a Brønsted acid is provided. This method for aldol reaction in water uses a catalytic amount of the boron source to give products in high yield and selectivity.

Abstract: Nonmetallic, chiral organic catalysts are used to catalyze the 1,4-hydride reduction of an ?,?-unsaturated carbonyl compound. The ?,?-unsaturated carbonyl compound may be an aldehyde or cyclic ketone, and the hydride donor may be a dihydropyridine. The reaction is enantioselective, and proceeds with a variety of hydride donors, catalysts, and substrates. The invention also provides compositions effective in carrying out the 1,4-hydride addition of ?,?-unsaturated carbonyl compounds.

Abstract: The present invention provides a process for the double metal cyanide (DMC)-catalyzed production of low unsaturation polyethers from boron-containing starters. The polyethers produced by the inventive process may be reacted with one or more isocyanates to provide polyurethane products including coatings, adhesives, sealants, elastomers, foams and the like. The inventive process may be used to prepare fuel additives from C9-C30 boron-containing polyethers, more particularly from C13 alcohols.

Abstract: 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 and is a straight or branched aliphatic group, or a cyclic, heterocyclic or aromatic group. R3 and R4 are each independently H or CH3. Mixtures of these compounds, methods for their preparation, their use as perfume materials for application to a variety of substrates and their use in flavoring and in articles of manufacture is also provided.

Abstract: A process for preparing (+)-p-mentha-2,8-diene-1-ol comprising reacting (+)-limonene oxide with at least one amine in the presence of at least one Lewis acid to form amine adduct intermediates. The amine adduct is then oxidized to form an N-oxide that is pyrolized to form (+)-p-mentha-2,8-diene-1-ol.

Abstract: One aspect of the present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-sulfur bond between the sulfur atom of a thiol moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper(II)-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-carbon bond between the carbon atom of cyanide ion and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate.

Abstract: The invention provides the use of compounds of the formula (1) where R1, R2 are each independently C1- to C22-alkyl, C2- to C22-alkenyl, C6- to C30-aryl or C7- to C30-alkylaryl, R3 is C1- to C22-alkyl, C2- to C22-alkenyl, C6- to C30-aryl or C7- to C30-alkylaryl, —CHR6COO? or —O?, A is a C2- to C4-alkylene group, B is a C1- to C10-alkylene group, X is O or NR7 R6, R7 are each independently hydrogen, C1- to C22-alkyl, C2- to C22-alkenyl, C6- to C30-aryl or C7- to C30-alkylaryl, R4 is a C1- to C50-alkyl, C2- to C50-alkenyl radical, C6- to C50-aryl or C7- to C50-alkylaryl, R5 is hydrogen, —OH or a C1- to C4-alkyl radical, n, m are each independently a number from 0 to 30, x is a number from 1 to 6, as corrosion and gas hydrate inhibitors, and also the compounds of formula 1.

Abstract: A process for synthesizing a naphthacene compound comprises the steps of: (a) reacting a propargyl alcohol compound with a reagent capable of forming a leaving group to form a reaction mixture containing an intermediate; and then (b) heating the intermediate in the presence of a solvent and in the absence of any oxidizing agent and in the absence of any base, to form the naphthacene compound.

Abstract: A process for producing an olefin oligomer, which comprises the steps of (1) contacting an olefin with an organoaluminum compound to produce a contact product (i), (2) contacting a transition metal compound with a compound represented by the formula, R1R2A-G-AR3R4, to produce a contact product (ii), and (3) contacting the contact product (i), the contact product (ii), an alumoxane compound, and optionally an olefin with one another, wherein A is a nitrogen atom, a phosphorus atom, an arsenic atom or an antimony atom, and As are the same as or different from each other; G is a divalent group; and R1, R2, R3 and R4 are independently of one another a hydrocarbyl group, a halogenated hydrocarbyl group, an oxygen-containing hydrocarbyl group, a sulfur-containing hydrocarbyl group, a selenium-containing hydrocarbyl group, or a tellurium-containing hydrocarbyl group.

Abstract: This invention is directed to a process for condensing and removing condensable compounds from an olefin stream containing light olefin compounds, and recovering the light olefin compounds. The process of the invention is particularly effective in removing water and heavy hydrocarbons, particularly aromatic hydrocarbons, from an olefin stream made from the catalytic conversion of oxygenate, and recovering light olefins such as ethylene, propylene, butylene, or a mixture thereof.

Abstract: The invention relates to a method and system for the treatment of radioactive wastes produced as a consequence of the operation of nuclear power plants with pressurized water reactors and boron reactivity regulation accompanied by the simultaneous production of environmentally acceptable substances of, for example, borax, calcium-magnesium borates, boron acid and sodium hydroxide solutions.

Abstract: The invention relates to a dressing or bandage comprising a dispersion of at least one transition metal in an imogolite or allophane matrix. In particular, it is intended for the manufacture of transparent dressings.

Abstract: An absorbent article having a first liquid permeable surface layer, a essentially liquid impermeable backing layer and, located between said liquid permeable surface layer and said liquid impermeable backing layer, an absorbent body having at least one layer. The absorbent article has cavities which are essentially cone-shaped and extend at least through part of the absorbent body, said cavities having a tip part and a base, the tip part being located towards or in the liquid permeable surface layer and the base being located away from the liquid permeable surface layer. A method of production of an absorbent article with cone-shaped cavities is also provided.

Abstract: The invention relates to genetically manipulated animals that are deficient in the expression of Caspase-9, a protein involved in programmed cell death. The invention further relates to methods for preventing specific types of cell death associated with Caspase-9 activation.

Abstract: A transgenic mouse whose genome comprises a Tie-2 promoter operably linked to a cDNA encoding calreticulin (CRT) is described.

Abstract: Transgenes encoding exogenous proteins are stably integrated into embryonic stem cells and are present in the somatic tissue of transgenic or chimeric birds. The transgenes encode exogenous proteins and are expressed in any of endodermal, ectodermal, mesodermal, or extra embryonic tissue. Tissue specificity is provided by selecting the content of the transgene accordingly. Transgenic birds whose genome is comprised of trangene derived exogenous DNA express exogenous proteins with tissue specificity, and specifically express exogenous proteins in the tubular gland cells of the oviduct to concentrate exogenous proteins in egg white.

Abstract: The present invention relates to methods for producing transgenic animals, particularly transgenic birds and fish, using retroviral constructs engineered to carry the transgene(s) of interest.

Abstract: A method for activating an equine oocyte comprising exposing oocyte to a medium containing a concentration of calcium of at least about 4 mM. Preferably the oocyte is exposed to this concentration of calcium during activation.

Abstract: This invention pertains to methods for decreasing the ratio of liquiritigenin-derived isoflavones relative to total isoflavone levels in isoflavonoid-producing plants and plant parts by transforming plants with a recombinant DNA construct comprising a nucleic acid sequence of at least 200 nucleotides and having at least 75% sequence identity to a polynucleotide encoding a chalcone reductase. More preferably, this invention pertains to methods for decreasing the ratios of daidzein and glycitein and their conjugates relative to total isoflavone levels in soybean plants and soybean plant parts by transforming plants with a recombinant DNA construct comprising a nucleic acid sequence of at least 200 nucleotides and having at least 75% sequence identity to a polynucleotide encoding a chalcone reductase.

Abstract: The invention is directed to isolated promoters from stem-regulated, defense-inducible genes, such as OMT promoters. The promoters are useful in expression cassettes and expression vectors for the transformation of plants. Particularly, the invention provides transgenic plants of rice and sugarcane that have been modified such that expression of a heterologous coding sequence is directed by an OMT promoter and is limited to stem tissues or may be upregulated by the presence of a defense-inducing agent. The invention also discloses methods for producing the expression vectors and transgenic plants.

Abstract: The present invention is directed to nucleic acid molecules tat encode defensive polypeptides and methods of their use in enhancing disease resistance of a plant to a fungal pathogen. Vectors, expression cassettes, viruses, cells, and plants comprising a nucleotide sequence of the invention are farther provided.

Abstract: The invention relates to a method for influencing the sinapine content in transgenic plant cells and plants. In particular, the invention relates to the inhibition of the enzymatic activity of a UDP-glucose: sinapate glucosyltransferase (SGT) in transgenic plant cells. The invention further relates to nucleic acid molecules containing a DNA sequence which codes for a protein with the enzymatic activity of an SGT. The invention furthermore relates to transgenic plants and plant cells comprising a nucleic acid molecule according to the invention, as a result of which contain a lower content of sinapine in comparison with wild-type plants or cells, and the agricultural products and propagating material of the transgenic plants.

Abstract: A novel pea cultivar, designated FP2280, is disclosed. The invention relates to the seeds of pea cultivar FP2280, to the plants of pea line FP2280 and to methods for producing a pea plant by crossing the cultivar FP2280 with itself or another pea line. The invention further relates to methods for producing a pea plant containing in its genetic material one or more transgenes and to the transgenic plants produced by that method and to methods for producing other pea lines derived from the cultivar FP2280.

Abstract: Basically, this invention provides for an inbred corn line designated G06-NP2623, methods for producing a corn plant by crossing plants of the inbred line G06-NP2623 with plants of another corn plants. The invention relates to the various parts of inbred G06-NP2623 including culturable cells. This invention also relates to methods for introducing transgenic transgenes into inbred corn line G06-NP2623 and plants produced by said methods.

Abstract: A permanent, flexible, self-adhesive, non-slip pad, the pad being made of material which can be affixed to the body of a stringed musical instrument to prevent the instrument from slipping in any direction on a player's clothing while the player is in a sitting or standing playing position.

Abstract: A front board, side boards and a rear board define the periphery of a cabinet for a keyboard musical instrument; a top board is connected to the front board through a mortise and tenon joint, and is further coupled to rear posts by means of an angle bar and bolts; the tenon is easily inserted into the mortise so as to make the assembling work easy and speedy.

Abstract: Systems and methods for performing simple and quick real time single music note recognition algorithm based on fuzzy pattern matching are disclosed. In one aspect, the systems and methods use a 256-point FFT and fuzzy pattern identification and recognition method. The systems and methods can recognize a note as short as 0.125 seconds in a frequency range from 16 Hz to 4000 Hz, with 11.025 KHz sampling rate and 8-bit per sampling signal. The systems and methods may be used as part of a music tutor system that receives a played note, identifies the played note, and compares the played note with a reference note. An indication may be given as to whether the played note matched the reference note.

Abstract: An automatic musical performance system stores musical data such as performance patterns and pattern sequences. During performance, the user provides input indicating tones to be added to or deleted from the musical performance, and the stored musical data is updated in accordance with the user input by adding or deleting the specified tones from the performance at the locations within the performance at which the user input for each tone was received.

Abstract: In an instrument performance learning apparatus, a storage section stores model performance waveform data representing a time series of individual performance sounds of a model performance. An input section inputs real performance waveform data representing a time series of individual performance sounds of a real performance. A pitch graph display control section detects each pitch of each individual performance sound from the stored model performance waveform data and from the inputted real performance waveform data, and displays a pitch graph representing transitions of the detected pitches.

Abstract: A ring-shaped percussion transducer for converting a striking impact into a representative electrical pulse triggering signal is suitable for mounting on the center axis of a percussion instrument. In a preferred embodiment, the transducer is formed of a piezo electric material of ring shape; protected on the top and bottom by thinner ring shaped washers; enclosed in a protective coating and mounted along the center axis of a percussion device which when struck transmits vibrations to the percussion transducer. The percussion transducer is connected to conventional downstream electronics so as to produce a sound responsive to the striking impact.

Abstract: The invention provides systems and methods of for displaying on a second instrument finger positions that were played on a first instrument. A teacher, for example, can play notes and/or chords on a first stringed instrument having a sensor. A processing having a decoder and a message generator can receive signals from the sensor and generate messages that are communicated to a light-system in the second instrument. The light-system displays the finger positions on the second instrument, each finger position corresponding to a finger position played on the first instrument. The processor can receive sensor information from the second information that can be used to determine whether a displayed finger position was correctly played on the second instrument.

Abstract: A method of forming an electronic circuit component using the technique of drop on demand printing to deposit droplets of deposition material, said method comprising depositing a plurality of droplets on a surface to form a patterned electronic device comprising multiple discrete portions.

Abstract: A method of making a photovoltaic cell includes contacting a cross-linking agent with semiconductor particles, and incorporating the semiconductor particles into the photovoltaic cell.

Abstract: An aerial cable spacer is provided with a cable retainer and vertically disposed strengthening tabs or ribs. The cable retainer includes a cable retaining arm. A mid portion of the cable retaining arm has a non-rectangular plus “+” shaped cross section. The plus “+” shaped cross section engages and exerts a force on the cable as the cable retaining arm bends to a closed position. The arm is flexible so as to create a resilient force in conjunction with the plus “+” shaped cross section to securely hold the cable on a cable seat of a main body portion of the aerial cable spacer. A pawl is carried on the arm at a predetermined orientation to engage a corresponding set of teeth on the spacer body for enhanced cable clamping force.

Abstract: A roller is provided in combination with an electrical junction box to facilitate pulling of wires through the box. The roller has a spring mounted plunger on one end adapted to be received within a pre-existing hole in a side wall of the box, and a press-fit stud on the opposite end to be received within a pre-existing hole on the opposite side wall of the box. The plunger and stud rotatably support the roller within the box so that wires can be pulled over the roller by a person at a location remote from the junction box. The roller can be quickly and easily installed in the junction box using only one hand.

Abstract: A modular wiring system including a wall box receptacle device. The system includes a wiring interface disposed on a first side and electrically coupled to a plurality of receptacle openings disposed on a second side. An adjustable support assembly includes a retaining frame configured to secure the wall box receptacle device therein. A first hinged mounting member is rotatably coupled to a first end of the retaining frame, and a second hinged mounting member is rotatably coupled to a second end of the retaining frame. A modular electrical wiring device includes at least one electrical circuit disposed between a cover member and a rear body member. The at least one electrical circuit is coupled to a plurality of male terminal elements accessibly disposed in the rear body member. The plurality of terminal blades are insertable in the plurality of receptacle openings to establish electrical continuity between the plurality of male terminal elements and the wiring interface.