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  • Lipoic acid  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 61-66 
    ISSN: 1434-1948
    Keywords: Arsenic ; Bioinorganic chemistry ; Dihydrolipoic acid ; Lipoic acid ; S ligands ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The arsenic(III) dithiolate [PhAs(HlipS2)] (1, HlipS2-2 = reduced rac-lipoic acid) has been obtained via three different routes: (A) from (PhAsO)n and rac-dihydrolipoic acid, (B) from (AsPh)6 and rac-lipoic acid, and (C) from PhAsO(OH)2 and rac-dihydrolipoic acid. The latter method is also suitable for the preparation of [(4-NH2C6H4)As(HlipS2)] (2) from (4-NH2C6H4)AsO(OH)2. rac-Dihydrolipoic acid and Me2AsO(OH) react to give [(Me2As)2(HlipS2)] (3). These reactions indicate pathways by which mono- and diorganoarsenic compounds of various As oxidation states (I, III, and V) may inhibit enzymes that contain lipoic acid as a cofactor. X-ray structure analysis shows that 1 is a 2,4-disubstituted 1,3,2-dithiarsinane, i. e. a six-membered heterocycle. The phenyl group at the 2-position (As) adopts the axial orientation. (2RS,4RS)-1, which is the isomer found in the crystal, is thermodynamically more stable than the diastereomeric (2SR,4RS)-1 by 4.3 ± 0.8 kJ/mol (25°C). In solution, the epimerization by inversion of configuration at the ψ-tetrahedrally coordinated As atom is faster than expected, with acid catalysis (COOH groups!) being a possible cause.
    Type of Medium: Electronic Resource
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