Synlett 1999; 1999(4): 495-497
DOI: 10.1055/s-1999-2624
letter
© 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.

An Improved Synthesis of Substituted Rubicenes Providing Access to Heterocyclic Rubicene Analogues

Mario Smet* , Joachim Van Dijk, Wim Dehaen
  • *Katholieke Universiteit Leuven, Laboratory for organic synthesis, Celestijnenlaan 200F, 3001 Leuven (Heverlee), Belgium; Fax 32 16 32 79 90; E-mail: Wim.Dehaen@chem.kuleuven.ac.be
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
31. Dezember 1999 (online)

A new method for the preparation of substituted 9,10-diarylanthracenes is described. These compounds are ring closed under palladium catalysis yielding the novel asymmetrically substituted rubicenes and heterocyclic rubicene analogoues.