Download PDF
Synlett 1993; 1993(9): 672-674
DOI: 10.1055/s-1993-22567
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.

Microbial Oxidation of Benzene as a Route to Inositol Stereoisomers and (±)-Quebrachitol

Howard A. J. Carless* , K. Busia, O. Z. Oak
  • *Department of Chemistry, Birkbeck College, Gordon House, 29 Gordon Square, London WC1H 0PP, England
Further Information

Publication History

Publication Date:
19 March 2002 (online)

  PDF Download  Permissions and Reprints All articles of this category

Microbial oxidation of benzene and singlet oxygen reaction of the resulting cis-cyclohexa-3,5-diene-1,2-diol have been used in the synthesis of four inositols (the muco, allo, epi and (±)-chiro isomers) and of the 2-O-methyl-chiro-inositol, (±)-quebrachitol.

      >