Issue 19, 2014
From the journal:

RSC Advances

Cooperative effect in organocatalytic intramolecular hydroamination of unfunctionalized olefins†

Yu-Mei Wang,a   Ting-Ting Li,a   Gong-Qing Liu,a   Li Zhang,a   Lili Duan,a   Lin Lia  and  Yue-Ming Li*a  

* Corresponding authors

a College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, 94 Weijin Road, Tianjin 300071, People's Republic of China
E-mail: ymli@nankai.edu.cn
Fax: +86 22 23507760
Tel: +86 22 23504028

Abstract

The cooperative effect in organocatalytic hydroamination of unfunctionalized olefins was reported. In the presence of 3-hydroxy-2-naphthoic acid, N-benzyl 4-penten-1-amines and 5-hexen-1-amines produced the intramolecular cyclization products in good isolated yields.

Graphical abstract: Cooperative effect in organocatalytic intramolecular hydroamination of unfunctionalized olefins

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C3RA47060A
Article type
Communication
Submitted
26 Nov 2013
Accepted
21 Jan 2014
First published
23 Jan 2014

RSC Adv., 2014,4, 9517-9521

Permissions

Request permissions

Cooperative effect in organocatalytic intramolecular hydroamination of unfunctionalized olefins

Y. Wang, T. Li, G. Liu, L. Zhang, L. Duan, L. Li and Y. Li, RSC Adv., 2014, 4, 9517 DOI: 10.1039/C3RA47060A

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