Abstract: The present invention relates to a method for preparing 2?-O-fucosyllactose, the 2?-O-fucosyllactose obtainable by this method and the use thereof. The method comprises reacting the persilylated, protected fucose derivatives of the formula (I) below, with at least one tri(C1-C6-alkyl)silyl iodide and subsequently reacting the product thus obtained with the compound of the general formula (II), in the presence of a base. In the formulae (I) and (II), the variables are each defined as follows: RSi are the same or different and are a residue of the formula SiRaRbRc; R1 is a C(?O)—R11 residue or an SiR12R13R14 residue, R2 are the same or different and are C1-C8-alkyl or together form a linear C3-C6-alkanediyl, which is unsubstituted or has 1 to 6 methyl groups as substituents; R3 are the same or different and are C1-C8-alkyl or together form a linear C1-C4-alkanediyl, which is unsubstituted or has 1 to 6 methyl groups as substituents.

Abstract: The present invention relates to a method for preparing 2?-O-fucosyllactose, the 2?-O-fucosyllactose obtainable by this method and the use thereof. The method comprises reacting the persilylated, protected fucose derivatives of the formula (I) below, with at least one tri(C1-C6-alkyl)silyl iodide and subsequently reacting the product thus obtained with the compound of the general formula (II), in the presence of a base. In the formulae (I) and (II), the variables are each defined as follows: RSi are the same or different and are a residue of the formula SiRaRbRc; R1 is a C(?O)—R11 residue or an SiR12R13R14 residue, R2 are the same or different and are C1-C8-alkyl or together form a linear C3-C6-alkanediyl, which is unsubstituted or has 1 to 6 methyl groups as substituents; R3 are the same or different and are C1-C8-alkyl or together form a linear C1-C4-alkanediyl, which is unsubstituted or has 1 to 6 methyl groups as substituents.

Abstract: A method of preparing a compound of formula (IV) where R1 is alkyl of 1 to 4 carbon atoms, comprises reacting cyclohexene with hydrogen peroxide and an alcohol R1OH in the presence of a catalyst comprising a zeolite of framework structure MWW, wherein the framework of the zeolite comprises silicon, titanium, boron, oxygen and hydrogen.

Abstract: The current invention is directed towards compounds of the general formula (I), wherein the integers are defined as follows: R1 is —(CH2)nCH(CH3)2, R2 is —(CH2)n+2CH(CH3)2, G1 selected from monosaccharides with 4 to 6 carbon atoms, x in the range of from 1.1 to 4, n is a number in the range of from zero to 3.

Abstract: The current invention is directed towards compounds of the general formula (I), wherein the integers are defined as follows: R1 is —(CH2)nCH(CH3)2, R2 is —(CH2)n+2CH(CH3)2, G1 selected from monosaccharides with 4 to 6 carbon atoms, x in the range of from 1.1 to 4, n is a number in the range of from zero to 3.

Abstract: Method for working up a mixture comprising at least one alcohol of the general formula (I) R1—CH2—CH2—OH??(I) or at least one branched alcohol of the general formula (II) R1—CH2—CH2—CHR1—CH2—OH??(II), furthermore at least one oil-soluble complex compound of at least one metal of the 8th, 9th or 10th group of the Periodic Table of the Elements, which is selected from complex compounds which have at least one ligand L1 which is at least bidentate, where at least one coordination site of L1 is a nitrogen atom, and at least one acid of the general formula (III) R1—CH2—COOH??(III) in the form of one of its salts, where the groups R1 are selected from C2-C10-alkyl, linear or branched, wherein (a) the mixture is treated with water which can comprise an alkali metal hydroxide, (b) the salt or salts of acid of the general formula (III) are extracted.

Abstract: Described is a process for simultaneously purifying fatty alcohols and obtaining a fraction of free fatty acids, wherein: (a) crude fatty alcohols comprising up to 70% b.w. alkyl esters and/or wax esters are treated with alkaline bases in an amount sufficient to essentially convert said esters into alkaline soaps, (b) said alkaline soaps are separated from said fatty alcohols by extraction to produce a purified fraction of fatty alcohols and an aqueous soap phase, and (c) said soap phase is treated with strong mineral acids in order to release the fatty acids from the soaps.

Abstract: Method for working up a mixture comprising at least one alcohol of the general formula (I) R1—CH2—CH2—OH??(I) or at least one branched alcohol of the general formula (II) R1—CH2—CHR1—CH2—OH??(II), furthermore at least one oil-soluble complex compound of at least one metal of the 8th, 9th or 10th group of the Periodic Table of the Elements, which is selected from complex compounds which have at least one ligand L1 which is at least bidentate, where at least one coordination site of L1 is a nitrogen atom, and at least one acid of the general formula (III) R1—CH2—COOH??(III) in the form of one of its salts, where the groups R1 are selected from C2-C10-alkyl, linear or branched, wherein (a) the mixture is treated with water which can comprise an alkali metal hydroxide, (b) the salt or salts of acid of the general formula (III) are extracted.

Abstract: Process for preparing branched alcohols of the general formula (I) where the groups R1 are different or identical and selected from C2-C3-alkyl, linear or branched, using at least one alcohol of the formula (II) R1—CH2—CH2—OH??(II) in homogeneous phase in the presence of at least one base, wherein at least one Ru(II)-containing complex compound is used in which the Ru(II) has at least one ligand L1 which is at least bidentate, where at least one coordination site of L1 is a nitrogen atom.

Abstract: Described is a process for simultaneously purifying fatty alcohols and obtaining a fraction of free fatty acids, wherein: (a) crude fatty alcohols comprising up to 70% b.w. alkyl esters and/or wax esters are treated with alkaline bases in an amount sufficient to essentially convert said esters into alkaline soaps, (b) said alkaline soaps are separated from said fatty alcohols by extraction to produce a purified fraction of fatty alcohols and an aqueous soap phase, and (c) said soap phase is treated with strong mineral acids in order to release the fatty acids from the soaps.