Synthetic studies on reidispongiolide A, an actin-depolymerizing marine macrolide: synthesis of C11-C22 and C23-C35 segments

  • Akiyama S
  • Toriihara E
  • Suzuki K
 et al. 
  • 5


    Mendeley users who have this article in their library.
  • 3


    Citations of this article.


The C11-C22 and C23-C35 segments 2 and 3 of reidispongiolide A (1), an actin-depolymerizing marine macrolide, were synthesized enantioselectively in 12 steps from (R)-glycidyl trityl ether and in 12 steps from chiral ketone 15, respectively. © 2009 Elsevier Ltd. All rights reserved.

Get free article suggestions today

Mendeley saves you time finding and organizing research

Sign up here
Already have an account ?Sign in

Find this document


  • Satoshi Akiyama

  • Eisuke Toriihara

  • Kazushi Suzuki

  • Toshiaki Teruya

  • Kiyotake Suenaga

Cite this document

Choose a citation style from the tabs below

Save time finding and organizing research with Mendeley

Sign up for free