Issue 13, 2007
From the journal:

Chemical Communications

Gold-catalyzed cyclo-isomerization of 1,6-diyne-4-en-3-ols to form naphthyl ketone derivatives†

Jian-Jou Liana  and  Rai-Shung Liu*a  

* Corresponding authors

a Department of Chemistry, National Tsing-Hua University, Hsinchu, Taiwan 300, ROC
E-mail: rsliu@mx.nthu.edu.tw
Fax: +886 3-5711082
Tel: +886 3-5721424

Abstract

We report a new efficient gold-catalyzed cyclization of 1,6-diyne-4-en-3-ols to give naphthyl ketone derivatives under ambient conditions. The value of this cyclization is reflected by its applicability to a wide range of alcohol substrates.

Graphical abstract: Gold-catalyzed cyclo-isomerization of 1,6-diyne-4-en-3-ols to form naphthyl ketone derivatives

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Article information

DOI
https://doi.org/10.1039/B618291G
Article type
Communication
Submitted
14 Dec 2006
Accepted
08 Jan 2007
First published
18 Jan 2007

Chem. Commun., 2007, 1337-1339

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Gold-catalyzed cyclo-isomerization of 1,6-diyne-4-en-3-ols to form naphthyl ketone derivatives

J. Lian and R. Liu, Chem. Commun., 2007, 1337 DOI: 10.1039/B618291G

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