Issue 42, 2013
From the journal:

Chemical Communications

Highly regioselective ring-opening coupling of diarylmethylenecyclopropa[b]naphthalenes with Grignard reagents†

Jian Cao,a   Xian Huang‡ab  and  Luling Wu*a  

* Corresponding authors

a Department of Chemistry, Zhejiang University, Hangzhou 310028, P. R. China
E-mail: wululing@zju.edu.cn

b State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, P. R. China

Abstract

Highly regioselective ring-opening coupling reactions of diarylmethylenecyclopropa[b]naphthalenes with Grignard reagents have been developed, which provide differently substituted β-vinylic naphthalenes in moderate to excellent yields.

Graphical abstract: Highly regioselective ring-opening coupling of diarylmethylenecyclopropa[b]naphthalenes with Grignard reagents

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Article information

DOI
https://doi.org/10.1039/C3CC00171G
Article type
Communication
Submitted
08 Jan 2013
Accepted
29 Mar 2013
First published
03 Apr 2013

Chem. Commun., 2013,49, 4788-4790

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Highly regioselective ring-opening coupling of diarylmethylenecyclopropa[b]naphthalenes with Grignard reagents

J. Cao, X. Huang and L. Wu, Chem. Commun., 2013, 49, 4788 DOI: 10.1039/C3CC00171G

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