54.
    发明专利
    未知

    公开(公告)号:DE50305771D1

    公开(公告)日:2007-01-04

    申请号:DE50305771

    申请日:2003-07-31

    Applicant: BASF AG

    Inventor: STUERMER RAINER

    Abstract: The present invention relates to a process for the preparation of enantiomerically pure (S)-3-methyl-amino-1-(thien-2-yl)propan-1-ol of the formula II-S by obtainment of (S)-3-hydroxy-3-thien-2-ylpropionitrile from its enantiomer mixture with the R isomer and the subsequent reaction of (S)-3-hydroxy-3-thien-2-ylpropionitrile with hydrogen and methylamine in the presence of a catalyst to give II-S.

    57.
    发明专利
    未知

    公开(公告)号:DE102004022686A1

    公开(公告)日:2005-11-24

    申请号:DE102004022686

    申请日:2004-05-05

    Applicant: BASF AG

    Abstract: The invention relates to a method for producing the optically active alkanols of formula (I), wherein n is an integer of from 0 to 5; Cyc represents an optionally substituted, mononuclear or polynuclear, saturated or unsaturated, carbocylic or heterocyclic ring, and R1 represents halogen, SH, OH, NO2, NR2R3 or NR2R3R4+X−, wherein R2, R3 and R4 independently represent H or a lower alkyl or lower alkoxy group and X− represents a counterion. According to the invention, an enzyme (E) selected from the groups of dehydrogenases, aldehyde reductases and carbonyl reductases is incubated in a medium containing the alkanone of formula (II), wherein n, Cyc and R1 are defined as above, in the presence of reduction equivalents. The compound of formula (II) is enzymatically reduced to the compound of formula (I) and the reduction equivalents consumed during reaction are regenerated by reacting a sacrificial alcohol to the corresponding sacrificial ketone using enzyme (E) and at least partially removing the sacrificial ketone from the reaction medium, and then isolating the product (I) so produced.

    60.
    发明专利
    未知

    公开(公告)号:AT260984T

    公开(公告)日:2004-03-15

    申请号:AT98109999

    申请日:1998-06-02

    Applicant: BASF AG

    Abstract: Production of acylated amino acid esters comprises acylating an amino acid ester with a carboxylic acid ester, which carries a halo, N, O or S atom in the neighbourhood of the carbonyl group of the acid component, in the presence of an amidase, protease, esterase or lipase as catalyst. Also claimed are (1) the production of optically active amino acid esters by: (a) enantioselectively acylating a racemic amino acid ester with a carboxylic acid ester, which carries a halo, N, O or S atom in the neighbourhood of the carbonyl group of the acid component, in the presence of an amidase, protease, esterase or lipase as catalyst; (b) separating the mixture obtained into optically active amino acid ester and optically active N-acyl-amino acid ester; and optionally (c) converting the optically active N-acyl-amino acid ester into the opposite amino acid ester enantiomer by amide cleavage; and (2) optically active amino acid esters of formula (I) and optically active N-acyl-amino acid esters of formula (II ) in which the NH2 and COOCH3 (or amino and COOR groups) are cis or trans to one another: R = 1-10C alkyl; 1-4C alkoxy; OH; NH2; halo; or Ar; R = H or 1-10C alkyl; X = halo; OR ; SR ; or NR R ; R and R = H; 1-10C alkyl; or Ar; R = 1-10C alkyl or Ar; Ar = aryl optionally substituted by NH2, OH, 1-4C alkyl, 1-4C alkoxy or halo; i = 0-4; m = 0-2; n = 1-3.

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