Abstract: Described herein is a method for preparing an amino salt compound, the method including: i) providing a carbonyl compound; ii) reacting the carbonyl compound provided according to (i) in the presence of a transaminase with ii-a) at least one primary amine; and ii-b) at least one carboxylic acid; thereby obtaining a mixture including an at least partially crystallized amino salt compound including a cation and a carboxylate anion based on the at least one carboxylic acid added according to (ii-b). Also described herein is an amino salt compound obtained or obtainable by the method and to the amino salt compound, and a composition including a) an amine of general formula (IIa); and b) at least one carboxylic acid of general formula (III).

Abstract: Described herein is a method for preparing an amino salt compound, the method including: i) providing a carbonyl compound; ii) reacting the carbonyl compound provided according to (i) in the presence of a transaminase with ii-a) at least one primary amine; and ii-b) at least one carboxylic acid; thereby obtaining a mixture including an at least partially crystallized amino salt compound including a cation and a carboxylate anion based on the at least one carboxylic acid added according to (ii-b). Also described herein is an amino salt compound obtained or obtainable by the method and to the amino salt compound, and a composition including a) an amine of general formula (IIa); and b) at least one carboxylic acid of general formula (III).

Abstract: The present invention relates to a process for producing bile acid derivatives having a protected hydroxyl group in the 3 position comprising contacting a bile acid derivative having an unprotected 3-alpha-hydroxyl group with a specific lipase. The present invention further relates to a bile acid derivative obtained or obtainable by the process, to the use of the bile acid derivative obtained or obtainable by the process for producing lithocholic acid and also to a process for producing lithocholic acid and to lithocholic obtained by the process. The invention further relates to the use of lithocholic acid obtained or obtainable by the process for producing ursodeoxycholic acid or ursodeoxycholic acid derivatives.

Abstract: The invention relates to an effective method of separating polycyclic aromatic hydrocarbons by means of a chromatographic separation method. This is achieved by using, according to the invention, calixarene-modified separation phases as stationary phase for chromatography in order to separate polycyclic aromatic hydrocarbons. The calixarene-modified stationary phases are particularly suitable for separating polycyclic aromatic hydrocarbons in liquid chromatography separation methods.

Abstract: The invention relates to a method for the modification of stationary phases which contain silanol groups with calixarene for chromatography. The silanol groups in these phases, preferably silica gel or glass, are, according to the invention, first reacted with a dialkylsilane so that a maximum number of the silanol groups of the stationary phase is modified, and then linkage takes place, by means of heterogeneous hydrosilylation, between an olefinic group which is present in the calixarene and the silane functionality of the prepared stationary phase in the presence of one or more noble metal catalysts.The invention's area of application is in column chromatography, including HPLC, thin-layer chromatography, including HPTLC, and thick-layer chromatography and gas chromatography with packed columns.