Issue 21, 2011
From the journal:

Organic & Biomolecular Chemistry

Copper(i)-catalyzed synthesis of 1,3-enynes via coupling between vinyl halides and alkynes or domino coupling of vinyl halides†

Yan Zhu,a   Tingyi Li,a   Xiaoming Qu,a   Peng Sun,a   Hailong Yanga  and  Jincheng Mao*a  

* Corresponding authors

a Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, P. R. China
E-mail: jcmao@suda.edu.cn

Abstract

1,3-Enynes were easily prepared from coupling between vinyl halides and alkynes or domino coupling of vinyl halides in the presence of copper iodide. It is noteworthy that the double-bond geometry of the vinyl halides was retained during the reaction. This ligand-free protocol is potentially useful and practical.

Graphical abstract: Copper(i)-catalyzed synthesis of 1,3-enynes via coupling between vinyl halides and alkynes or domino coupling of vinyl halides

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C1OB06210G
Article type
Communication
Submitted
20 Jul 2011
Accepted
31 Aug 2011
First published
01 Sep 2011

Org. Biomol. Chem., 2011,9, 7309-7312

Permissions

Request permissions

Copper(I)-catalyzed synthesis of 1,3-enynes via coupling between vinyl halides and alkynes or domino coupling of vinyl halides

Y. Zhu, T. Li, X. Qu, P. Sun, H. Yang and J. Mao, Org. Biomol. Chem., 2011, 9, 7309 DOI: 10.1039/C1OB06210G

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements