Download PDF
Synlett 1993; 1993(4): 289-290
DOI: 10.1055/s-1993-22435
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.

Regioselective Oxidation of Glycals with Hypervalent Iodine Reagents

Andreas Kirschning* , Gerald Dräger, Jan Harders
  • *Institut für Organische Chemie der Technischen Universität Clausthal, Leibnizstrasse 6, W-3392 Clausthal-Zellerfeld, Germany
Further Information

Publication History

Publication Date:
19 March 2002 (online)

  PDF Download  Permissions and Reprints All articles of this category

The direct regioselective synthesis of hex-1-enopyran-3-uloses 3, 6, 8, and 10 by oxidation of the corresponding per-O-acylated and per-O-benzylated glycals 1, 4, 5, 7, and 9 is described. The method involves the use of [hydroxy(tosyloxy)-iodo]benzene 2.

      >