Issue 31, 2009
From the journal:

Chemical Communications

Tandem reactions of cis-2-acyl-1-alkynyl-1-aryl cyclopropanes tuned by gold(i) and silver(i) catalysts: efficient synthesis of pyran-fused indene cores and 2,4,6-trisubstituted phenols†

Xiao-Ming Zhang,a   Yong-Qiang Tu,*a   Yi-Jun Jiang,a   Yong-Qiang Zhang,a   Chun-An Fana  and  Fu-Min Zhang*a  

* Corresponding authors

a State Key Laboratory of Applied Organic Chemistry & Department of Chemistry, Lanzhou University, Lanzhou 730000, P. R. China
E-mail: tuyq@lzu.edu.cn
Fax: +86 931-8915557

Abstract

Tandem reactions of cis-2-acyl-1-alkynyl-1-aryl cyclopropanes 1 tuned by gold(I) and silver(I) catalysts are described, which afford selectively the key pyran-fused indene cores 2 and the 2,4,6-trisubstituted phenols 3 in good yields, respectively.

Graphical abstract: Tandem reactions of cis-2-acyl-1-alkynyl-1-aryl cyclopropanes tuned by gold(i) and silver(i) catalysts: efficient synthesis of pyran-fused indene cores and 2,4,6-trisubstituted phenols

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Article information

DOI
https://doi.org/10.1039/B909181E
Article type
Communication
Submitted
08 May 2009
Accepted
05 Jun 2009
First published
29 Jun 2009

Chem. Commun., 2009, 4726-4728

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Tandem reactions of cis-2-acyl-1-alkynyl-1-aryl cyclopropanes tuned by gold(I) and silver(I) catalysts: efficient synthesis of pyran-fused indene cores and 2,4,6-trisubstituted phenols

X. Zhang, Y. Tu, Y. Jiang, Y. Zhang, C. Fan and F. Zhang, Chem. Commun., 2009, 4726 DOI: 10.1039/B909181E

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