Chemistry Letters
Online ISSN : 1348-0715
Print ISSN : 0366-7022
ISSN-L : 0366-7022
Stereoselective Synthesis of the LM Ring Moiety of Ciguatoxin: Reagent Control of Asymmetric Dihydroxylation
Tohru OishiMitsuru ShojiNaomi KumaharaMasahiro Hirama
Author information
JOURNALS RESTRICTED ACCESS

1997 Volume 26 Issue 9 Pages 845-846

Details
Abstract

Stereoselective synthesis of the LM ring moiety of ciguatoxin was achieved from (R)-(E)-1-benzyloxy-2-hydroxy-3-pentene via Ireland-Claisen rearrangement, iodolactonization, and reagent-controlled asymmetric dihydroxylation.

Information related to the author

This article cannot obtain the latest cited-by information.

© 1997 The Chemical Society of Japan
Previous article Next article
feedback
Top