Issue 15, 2011
From the journal:

Chemical Communications

Ring-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles†

Minghao Li,a   Conghui Tang,a   Jie Yanga  and  Yanlong Gu*ab  

* Corresponding authors

a Institute of Physical Chemistry and Industrial Catalysis, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, 1037 Luoyu road, Hongshan District, Wuhan 430074, China
E-mail: klgyl@hust.edu.cn
Fax: (+)(0)86-(0)27-87 54 45 32

b State Key Laboratory for Oxo Synthesis and Selective Oxidation, Lanzhou Institute of Chemical Physics, Lanzhou, China

Abstract

Ring-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles were reported for the first time. A possible mechanism was also proposed. Finally, this method was used in the synthesis of a novel tetrahydrocarbazole derivative that possesses a biologically active skeleton.

Graphical abstract: Ring-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles

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Article information

DOI
https://doi.org/10.1039/C1CC10355E
Article type
Communication
Submitted
19 Jan 2011
Accepted
25 Feb 2011
First published
14 Mar 2011

Chem. Commun., 2011,47, 4529-4531

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Ring-opening reactions of 2-aryl-3, 4-dihydropyrans with nucleophiles

M. Li, C. Tang, J. Yang and Y. Gu, Chem. Commun., 2011, 47, 4529 DOI: 10.1039/C1CC10355E

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