Abstract: A process is proposed for preparing unsaturated macrocyclic monoketones, comprising the following steps: (a) providing macrocyclic dienes having a ring size of at least 9 carbon atoms; (b) contacting the starting materials from step (a) with (b1) a palladium(II) salt and/or a palladium(II) complex; and (b2) an oxidizing agent; and (b3) a solvent; and optionally (b4) a ligand; and optionally (b5) a co-catalyst; and optionally (b6) an acid, with the proviso that the co-catalyst (b5) comprises or consists of a divalent or trivalent iron salt which is different from FeSO4 and is preferably iron(III) nitrate.

Abstract: The present invention relates to a process for the production of glycolaldehyde by thermolytic fragmentation of a carbohydrate feedstock comprising mono- and/or di-saccharide(s) and a system suitable for performing the process. The process and the system are suitable for industrial application, and the process may be performed in a continuous process.

Abstract: The invention relates to a method for transferring a target substance (5), particularly a target molecule (5), between two liquid phases (4, 6; 6, 8; 6, 11), of which at least one phase (4, 6) comprises the target substance (5) to be transferred and at least one phase (4, 8, 11) is an aqueous phase, where at least the aqueous phase (4, 8, 11) is arranged in one of two electrode chambers (1a, 1b, 10a, 10b) which are electroconductively connected, preferably by charge carrier exchange, and separated in terms of the volumes thereof, preferably where the phases (4, 6; 6, 8; 6, 11) are arranged together in one of two electrode chambers (1a, 1b, 10a, 10b) which are electroconductively connected and separated in terms of the volumes thereof, and a pH-value modification is generated by the H and/or OH ions created during the electrolysis in the aqueous phase (4, 8, 11), said modification initiating a transfer process of the target substance (5) between the phases (4, 6; 6, 8; 6, 11).

Abstract: The present disclosure provides methods for selectively crystallizing cannabinoids from solutions containing a plurality of cannabinoids. The present disclosure further provides methods for separating a crystallized cannabinoid from a mixture of cannabinoids.

Abstract: A cocrystal having the formula LiX.aM, or a solvate or hydrate thereof, wherein X is a conjugate base of an organic acid, M is a neutral organic molecule, and a is from 0.5 to 4, pharmaceutical compositions comprising such cocrystals, cocrystal solvates, or cocrystal hydrates, and methods of preparing such cocrystals, cocrystal solvates, or cocrystal hydrates, and such pharmaceutical compositions.

Abstract: An article that includes a functionalized copolymer and the use thereof, particularly in a process for binding biomaterials, such as in a process for separating aggregated proteins from monomeric proteins in a biological solution; wherein the article includes: a) a porous substrate; and b) a copolymer covalently attached to the porous substrate, the copolymer comprising a hydrocarbon backbone and a plurality of pendant groups attached to the hydrocarbon backbone, wherein 1) each of a first plurality of pendant groups comprises: (a) at least one acidic group or salt thereof; and (b) a spacer group that directly links the at least one acidic group or salt thereof to the hydrocarbon backbone by a chain of at least 6 catenated atoms; and 2) each of a second plurality of pendant groups comprises: (a) at least one acidic group or salt thereof; and (b) a spacer group that directly links the at least one acidic group or salt thereof to the hydrocarbon backbone by a chain of at least 6 catenated atoms; and wherein the

Abstract: The present invention relates to new classes of odorous ketones (odorants) which are useful as fragrance or flavor materials in particular in providing coniferous, thuya, floral and/or fruity olfactory notes to perfume, aroma or deodorizing/masking compositions.

Abstract: The present disclosure is directed to methods and systems of purifying solvents. The purified solvents can be used, e.g., as pre-wet liquids, solution developers, and cleaners in a multistep semiconductor manufacturing process.

Abstract: Embodiments may provide systems and method for purifying natural and/or organically certified nutraceuticals, such as cannabinoids. Embodiments may include refined or unrefined solvents, refined or unrefined plant extracts, refined or unrefined source compounds to be purified to any degree. Embodiments may reduce the concentration of impurities such as other cannabinoids (e.g., THC), terpenes, pesticides, herbicides, mycotoxins, heavy metals, other solvents (e.g., ethanol), waxes, or other impurities. Embodiments may increase the concentration of target compound(s) from its respective source material.

Abstract: A method for isolating curcuminoids from turmeric rhizome includes the steps of a) subjecting the turmeric rhizome to extraction with a first ethanol solution having an ethanol concentration ranging from 90% to 100% at a stirring speed ranging from 100 rpm to 300 rpm so as to obtain an ethanol-extracted product; and b) subjecting the ethanol-extracted product to crystallization with a second ethanol solution having an ethanol concentration ranging from 90% to 100 at a temperature ranging from 2° C. to 8° C. and a stirring speed ranging from 40 rpm to 300 rpm so as to obtain the curcuminoids.

Abstract: A method for manufacturing 1,4-bis(4-phenoxybenzoyl)benzene, including: providing a solvent, a Lewis acid, a first reactant and a second reactant, wherein the first reactant and the second reactant are respectively terephthaloyl chloride and diphenyl ether, or reversely; mixing the first reactant in the solvent to make a starting mixture; and, adding the second reactant to the starting mixture; wherein the Lewis acid is mixed, at least partly, to the starting mixture before adding the second reactant to the starting mixture, and/or wherein the Lewis acid is mixed, at least partly, with the second reactant and added together to the starting mixture, and wherein the temperature of the starting mixture is greater than 5° C. during at least part of the step of adding the second reactant to the starting mixture; so as to obtain a product mixture comprising a 1,4-bis(4-phenoxybenzoyl)benzene-Lewis acid complex.

Abstract: Enantiopure terphenyl presenting two ortho-located chiral axes having the following structural formula (I): their process of synthesis and their use as mono or bidentate ligands for asymmetric organometallic reactions, as organocatalysts, as chiral base and as generator, with metal, of isolable chiral metallic complexes for applications in asymmetric catalysis and others.

Abstract: Disclosed are methods of decreasing the concentration of a metal in a monomer composition including a bis(benzoyl)benzene, bis(benzoyl)benzene monomer compositions having a low total metal concentration, di-ketone polymers made from low metal bis(benzoyl)benzene monomers, and polymer compositions and shaped articles including the di-ketone polymers. It was surprisingly found that di-ketone polymers made by nucleophilic substitution of low metal bis(benzoyl)benzene monomers exhibit greater crystallinity, as compared with di-ketone polymers made with conventional monomers.

Abstract: The invention relates to a method for producing a specific hydroxyl compound by decarboxylating a specific carboxylic acid compound or a salt of said carboxylic acid compound in the absence of a catalyst and to a method for producing a bisphenol.

Abstract: The present invention provides a process for preparing a terminal conjugated alkadienal compound of the following general formula (5): CH2?CHCH?CH(CH2)aCHO ??(5) wherein “a” represents an integer of 1 to 15, from a dialkoxyalkenyl alkoxymethyl ether compound of the following general formula (1): R1CH2OCH2OCH2CH2CH?CH(CH2)aCH(OR2)(OR3) ??(1) wherein R1 represents a hydrogen atom, an n-alkyl group having 1 to 9 carbon atoms, or a phenyl group, R2 and R3 represent, independently of each other, a monovalent hydrocarbon group having 1 to 15 carbon atoms, or R2 and R3 may form together a divalent hydrocarbon group, R2-R3, having 2 to 10 carbon atoms, and “a” is as defined above.

Abstract: A tetracarbonyl cyclobutene dihydrate compound, having a chemical formula (I). A method of synthesizing the tetracarbonyl cyclobutene dihydrate compound, includes: a synthesis step, a separation step, and a purification step. The synthesis step includes: collecting and dissolving 0.5728 g of squaric acid, 2.7948 g of ammonium formate, and 0.0480 g of the palladium complex in 100 mL of anhydrous methanol, heating and stirring a resulting mixture to reflux for 48 hrs, and stopping the reaction. The separation step includes: performing column chromatography analysis on reaction products according to a volume ratio of dichloromethane to anhydrous methanol of 8:2, to obtain a target product. A method of using the tetracarbonyl cyclobutene dihydrate compound, includes: using tetracarbonyl cyclobutene dihydrate compound as a catalyst in addition reaction between ethyl pyruvate and nitromethane, where a conversion rate of ethyl pyruvate reaches 96.1%.

Abstract: The present disclosure provides a method for decomposing a phenolic by-product, the method including: a step S10 of feeding a phenolic by-product stream to a decomposition apparatus and thermally cracking the phenolic by-product stream; a step S20 of recovering an active ingredient from a top discharge stream of the decomposition apparatus and discharging a substance having a high boiling point through a bottom discharge stream of the decomposition apparatus; a step S30 of passing a part of the bottom discharge stream of the decomposition apparatus through a reboiler and then feeding the part of the bottom discharge stream of the decomposition apparatus to the decomposition apparatus and discharging a residual stream of the bottom discharge stream of the decomposition apparatus; and a step S40 of feeding a side discharge stream of the decomposition apparatus to the reboiler.

Abstract: The present invention relates to a crystal form of 3-(4-methyl-1H-imidazol-1-yl)-5-trifluoromethylaniline monohydrochloride and the use thereof. Specifically, disclosed are a crystal form A of a monohydrochloride anhydrous substance of 3-(4-methyl-1H-imidazol-1-yl)-5-trifluoromethylaniline monohydrochloride, a method for preparing the crystal form A and the use of the crystal form in the synthesis of nilotinib. The crystal form A of the present invention has good stability and purity, and can be directly used in the preparation and production of nilotinib. The method for preparing nilotinib in the present invention is easy to operate and has high industrial application value.

Abstract: This present disclosure relates to a process for producing an organic peroxide and isolating, purifying, and concentrating the sulfuric acid from the aqueous effluents of said organic peroxide production process.

Abstract: The present invention relates to: a method for converting a hydroxyl group of an alcohol; and a catalyst which makes the method possible.