C[BOND]C-Bond Formation in the α-Position to Nitrogen in Secondary Amines. Lithiodimethylnitrosamine

Authors

  • Prof. Dr. Dieter Seebach,

    1. Institut für Organische Chemie der Universität, 63 Giessen, Ludwigstrasse 21, (Germany)
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  • Dieter Enders

    Corresponding author
    1. Institut für Organische Chemie der Universität, 63 Giessen, Ludwigstrasse 21, (Germany)
    • Institut für Organische Chemie der Universität, 63 Giessen, Ludwigstrasse 21, (Germany)
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  • Most nitrosamines are organotropic carcinogens [1]. All manipulations must be carried out with due care. However, cancer research scientists are interested in testing new types of nitrosamines which might become available through organometallic derivatives. We thank Prof. Dr. H. Druckrey, Freiburg, and Dr. R. Preussmann, Heidelberg, for valuable discussions.—Financial support by the Fonds der Chemischen Industrie is appreciated.

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