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Natural Product Research
Formerly Natural Product Letters
Volume 31, 2017 - Issue 2
126
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Research Article

The structure proposed for apteniol D is different from that of the compound obtained by total synthesis

, , , , , & show all
Pages 163-168 | Received 09 Feb 2016, Accepted 28 Jul 2016, Published online: 25 Aug 2016
 

Abstract

We describe the synthesis of 4,4′-oxyneolignan, the proposed structure for naturally occurring apteniol D. The diphenyl ether moiety in 4,4′-oxyneolignan was formed via classical Ullmann ether synthesis using excess copper powder in N,N-dimethylacetamide. The spectral data of synthesised apteniol D show differences compared to those of naturally occurring apteniol D.

Acknowledgement

The authors would like to thank Enago (www.enago.jp) for the English language review.

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