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
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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 |
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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 |
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