A short synthesis of biologically active lignan analogues
Abstract
β-Benzyl-γ-butyrolactones were synthesized in four transition metal catalysed reactions from butynediol, and alkylated to afford new, biologically active lignan analogues.
* Corresponding authors
a
Institut für Organische Chemie und Strukturanalytik, Universität Potsdam, Karl-Liebknecht-Str. 24-25, D-14476, Golm, Germany.
E-mail:
peter@serv.chem.uni-potsdam.de
b Institut für Ernährungswissenschaften, Friedrich-Schiller-Universität Jena, Dornburger Str. 25, D-07743, Jena, Germany
β-Benzyl-γ-butyrolactones were synthesized in four transition metal catalysed reactions from butynediol, and alkylated to afford new, biologically active lignan analogues.
A short synthesis of biologically active lignan analogues
S. Kamlage, M. Sefkow, B. L. Pool-Zobel and M. G. Peter, Chem. Commun., 2001, 331 DOI: 10.1039/B008499I
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