Synlett 1999; 1999(10): 1523-1533
DOI: 10.1055/s-1999-2880
account
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Venturing into Catalysis Based Natural Product Synthesis

Alois Fürstner*
  • *Max-Planck-Institut für Kohlenforschung, D-45470 Mülheim/Ruhr, Germany; Fax + 49(2 08)3 06 29 80; E-mail: fuerstner@mpi-muelheim.mpg.de
Further Information

Publication History

Publication Date:
31 December 1999 (online)

Some total syntheses from our laboratory targeting structurally diverse and biologically active pyrrole alkaloids, furanoterpenes, macrolide antibiotics and carbohydrates are summarized. All of them rely on new and/or improved transition metal catalyzed transformations as the key steps, intend to minimize the total number of operations in the overall sequences, and aim at valorizing bulk chemicals.

    >