Download PDF
Synlett 1993; 1993(10): 737-738
DOI: 10.1055/s-1993-22589
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.

Synthesis of the 2,3-Disubstituted Maleic Anhydride Segment of Tautomycin

Yoshiyasu Ichikawa* , Atsushi Naganawa, Minoru Isobe
  • *Laboratory of Organic Chemistry, School of Agriculture, Nagoya University, Chikusa, Nagoya 464-01, Japan
Further Information

Publication History

Publication Date:
19 March 2002 (online)

  PDF Download  Permissions and Reprints All articles of this category

The 2,3-disubstituted maleic anhydride segment of tautomycin has been synthesized by oxidation of 3,4-disubstituted furan employing singlet oxygen.

      >