Issue 3, 2015
From the journal:

Chemical Communications

Ag(i)-catalyzed tandem [6+3] annulation/isomerization of isocyanoacetates with fulvenes: an expedient approach to synthesize fused dihydropyridines†

Zhao-Lin Hea  and  Chun-Jiang Wang*ab  

* Corresponding authors

a College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China
E-mail: cjwang@whu.edu.cn

b State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai, 230012, China

Abstract

An unprecedented Ag(I)-catalyzed tandem [6+3] cycloaddition/isomerization of isocyanoacetates with fulvenes has been developed, affording the fused dihydropyridine derivatives in good yields with exclusive regioselectivities.

Graphical abstract: Ag(i)-catalyzed tandem [6+3] annulation/isomerization of isocyanoacetates with fulvenes: an expedient approach to synthesize fused dihydropyridines

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Article information

DOI
https://doi.org/10.1039/C4CC08382B
Article type
Communication
Submitted
23 Oct 2014
Accepted
12 Nov 2014
First published
12 Nov 2014

Chem. Commun., 2015,51, 534-536

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Ag(I)-catalyzed tandem [6+3] annulation/isomerization of isocyanoacetates with fulvenes: an expedient approach to synthesize fused dihydropyridines

Z. He and C. Wang, Chem. Commun., 2015, 51, 534 DOI: 10.1039/C4CC08382B

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