Issue 22, 2007

Synthetic strategies to epoxydiynes and a key synthon of the neocarzinostatin chromophore

Abstract

We present herein our recent efforts towards the synthesis of epoxydiynes which represent an unusual structural feature of the neocarzinostatin chromophore. A number of different routes to these epoxydiynes have been explored with varying success. Ultimately a concise and convergent approach was developed, which involved the addition of an allenyl zinc bromide to propargylic ketones/aldehydes followed by epoxide formation. This new protocol enabled us to synthesise a fully elaborated epoxydiyne which will find application for our studies towards the total synthesis of the NCS chromophore.

Graphical abstract: Synthetic strategies to epoxydiynes and a key synthon of the neocarzinostatin chromophore

Supplementary files

Article information

Article type
Paper
Submitted
23 Jul 2007
Accepted
17 Sep 2007
First published
03 Oct 2007

Org. Biomol. Chem., 2007,5, 3703-3712

Synthetic strategies to epoxydiynes and a key synthon of the neocarzinostatin chromophore

O. Thominet, J. R. Baker, H. Britton, Z. C. Etheridge, M. G. Soscia and S. Caddick, Org. Biomol. Chem., 2007, 5, 3703 DOI: 10.1039/B711196G

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