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ASCA GmbH Angewandte Synthesechemie Adlershof
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  • I Steroides
  • II Prostaglandines
  • III Nucleosides
  • IV Further natural products
  • V Aliphatic, cycloaliphatic compounds
  • VI Nitrogen and sulfur containing heterocycles
  • VII β-Lactones
  • VIII Further compounds
  • IX Enzymatic and microbial syntheses
  • X Electrochemical syntheses
  • XI Macrocycles
  • XII Phosphorus containing compounds
  • XIII Analytical investigations
  • XIV Reviews

X Electrochemical syntheses

  1. K. -H. Schwarz, K. Kleiner, R. Ludwig, H. Schick,
    A Convenient Electrochemical Synthesis of β-Lactones,
    in: Novel Trends in Electroorganic Synthesis, edited by S. Torii, Kodansha, Tokyo, 1995, 71-74, ISBN 4-06-207503-2
  2. H. Schick, R. Ludwig, K. Kleiner, A. Kunath,
    Reactions of Electrochemically Generated Organometallics, 5.
    Synthesis of Substituted β-Lactones by a Reformatsky Reaction of Carbonyl Compounds, Phenyl α-Bromoalkanoates, and Indium,

    Tetrahedron 1995, 51, 2939-2946.
  3. H. Schick, R. Ludwig, K.-H. Schwarz, K. Kleiner, A. Kunath,
    Reactions of Electrochemically Generated Organometallics, 4.
    Synthesis of α,α,β,β-tetrasubstituted β-Lactones from Ketones, Ethyl α-Bromoisobutyrate and Indium or Zinc. – Factors Influencing the β-Lactone Formation in the Electrochemical and the Classical Procedure of the Reformatsky Reaction,

    J. Org. Chem. 1994, 59, 3161-3164.
  4. H. Schick, R. Ludwig, K.-H. Schwarz, K. Kleiner, A. Kunath,
    Reactions of Electrochemically Generated Organometallics, 3.
    Neuartige Synthese tetrasubstituierter β-Lactone: Die Verwendung von Indium
    in der elektrochemisch unterstützten Reformatsky-Reaktion,

    Angew. Chem. 1993, 105, 1218-1220; Angew. Chem. Int. Ed. Engl. 1993, 32, 1191-1193.
  5. K.-H. Schwarz, K. Kleiner, R. Ludwig, H. Schick,
    Reactions of Electrochemically Generated Organometallics, 2.
    The Use of Zinc, Tin, Aluminum, Indium, and Iron as Sacrificial Anodes in the Electrochemically Assisted Reformatsky Reaction of Ethyl 2-Bromoalkanoates with Succinic Anhydride,

    Chem. Ber. 1993, 126, 1247-1249.
  6. K.-H. Schwarz, K. Kleiner, R. Ludwig, H. Schick,
    Reactions of Electrochemically Generated Organometallics, 1.
    Electrochemically Supported Reformatsky Reaction: A Convenient Preparation of 2-Substituted 1-Ethyl 3-Oxoalkanedioates,

    J. Org. Chem. 1992, 57, 4013-4015.
  7. K.-H. Schwarz, K. Kleiner, R. Ludwig, E. Schrötter, H. Schick,
    Synthesis of Methyl (±)-2,3-O-Isopropylideneglycerate via Electrochemical Oxidation of (±)-1,2-O-Isopropylideneglycerol,
    Liebigs Ann. Chem. 1991, 503-504.
  8. H. Matschiner, R. Voigtländer, H. Schick, H. Lund,
    Electrochemical Reduction of 3-Chloro-2-cycloalkenones,
    Acta Chem. Scand. B 1980, 34, 136-138.

ASCA GmbH
Angewandte Synthesechemie Adlershof
Magnusstraße 11, D-12489 Berlin


Tel.: +49 30 6392 2070
Fax: +49 30 6392 4103
E-Mail: asca@asca-berlin.de

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