Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000084.xml
Synthesis 2000; 2000(11): 1557-1560
DOI: 10.1055/s-2000-7604
DOI: 10.1055/s-2000-7604
paper
© 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.
The Preparation of Rigid Linear Di- (and Tri-)catechol Derivatives
Further Information
Publication History
Publication Date:
31 December 2000 (online)
The aryl-bridged rigid rod-like di- and tricatechol ligands 1-5 were prepared by aryl-aryl coupling reactions. Hereby either Suzuki coupling strategies [starting with 2,3-dimethoxyphenylboronic acid (6) as an important building block] or oxidative coupling with methyltributylammonium permanganate were used to obtain the desired compounds.
catechol - chelating ligands - Suzuki coupling - oxidative coupling - ether cleavage