Issue 70, 2013
From the journal:

Chemical Communications

Functionalized heterocyclic scaffolds derived from Morita–Baylis–Hillman Acetates†

Huajian Zhu,a   Nana Shao,a   Tong Chena  and  Hongbin Zou*a  

* Corresponding authors

a Institute of Materia Medica, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China
E-mail: zouhb@zju.edu.cn
Fax: +86 571 8820 8835
Tel: +86 571 8820 8835

Abstract

Five series of heterocycles with extraordinary structural diversity have been regiospecifically synthesized from the same Morita–Baylis–Hillman Acetates (MBHAs). All four potential electrophilic sites (α, β, γ, δ) of MBHAs are proved to be reactive.

Graphical abstract: Functionalized heterocyclic scaffolds derived from Morita–Baylis–Hillman Acetates

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Article information

DOI
https://doi.org/10.1039/C3CC43285H
Article type
Communication
Submitted
03 May 2013
Accepted
03 Jul 2013
First published
23 Jul 2013

Chem. Commun., 2013,49, 7738-7740

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Functionalized heterocyclic scaffolds derived from Morita–Baylis–Hillman Acetates

H. Zhu, N. Shao, T. Chen and H. Zou, Chem. Commun., 2013, 49, 7738 DOI: 10.1039/C3CC43285H

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