Download PDF
Synlett 2001; 2001(5): 0691-0693
DOI: 10.1055/s-2001-13387
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.

Convergent Syntheses of the Enantiomeric CD- and JK-Ring Parts of Ciguatoxin

Kenshu Fujiwara* , Daisuke Takaoka, Kensuke Kusumi, Kentaro Kawai, Akio Murai
  • *Division of Chemistry, Graduate School of Science, Hokkaido University, Sapporo 060-0810, Japan; E-mail: fjwkn@sci.hokudai.ac.jp
Further Information

Publication History

Publication Date:
31 December 2001 (online)

  PDF Download  Permissions and Reprints All articles of this category

Convergent syntheses of the enantiomeric CD- and JK-ring parts of ciguatoxin, based on a coupling reaction between dithioacetal mono-S-oxide and aldehyde derivatives and reductive cyclization of the respective hydroxy ketones, have been achieved.

ciguatoxin - acyl anion equivalent - dithioacetal mono-S-oxide - convergent synthesis - reductive etherification

      >