Synthesis 1996; 1996(6): 699-701
DOI: 10.1055/s-1996-4281
short 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.

Transition Metal Catalyzed Oxidation; 8: 4-Allyl-Substituted 1,2-Naphthoquinones via Tandem ortho-Phenol Oxygenation and Oxy-Cope Rearrangement

Karsten Krohn* , Sven Bernhard
  • *Universität-GH Paderborn, Fachbereich 13, Chemie und Chemietechnik, Fachgebiet Organische Chemie, Warburger Str. 100, D-33098 Paderborn, Germany, Fax +49(5251)603245; E-mail kk@chemie.uni-paderborn.de
Further Information

Publication History

Publication Date:
31 December 2000 (online)

4-Allyl-1,2-naphthoquinones 3a-3d are prepared in one operation from 2-allyl-1-naphthols 2a-2d involving tandem zirconium-catalyzed tert-butyl hydroperoxide (TBHP) oxidation and oxy-Cope rearrangement.

    >