Synthetic studies toward potent cytotoxic agent amphidinolide B: synthesis of the entire Cl-C13 moiety of the bottom half

Chakraborty, Tushar K. ; Suresh, Vayalakkada R. (1997) Synthetic studies toward potent cytotoxic agent amphidinolide B: synthesis of the entire Cl-C13 moiety of the bottom half Chemistry Letters, 26 (6). pp. 565-566. ISSN 0366-7022

Full text not available from this repository.

Official URL: http://www.jstage.jst.go.jp/article/cl/26/6/26_565...

Related URL: http://dx.doi.org/10.1246/cl.1997.565

Abstract

Sharpless asymmetric dihydroxylation and Nozaki-Hiyama-Kishi's Cr(II)-mediated coupling between an α-alkoxyaldehyde and a vinyl iodide are the key steps in the stereoselective synthesis of the entire C1-C13 segment of the bottom-half of amphidinolide B.

Item Type:Article
Source:Copyright of this article belongs to Chemical Society of Japan.
ID Code:20620
Deposited On:20 Nov 2010 13:50
Last Modified:23 May 2011 03:53

Repository Staff Only: item control page