Issue 45, 2009
From the journal:

Chemical Communications

Iodine-mediated cyclization of N-thioacyl-1-(2-pyridyl)-1,2-aminoalcohols and their subsequent condensation leading to the formation of novel bis(1-imidazo[1,5-a]pyridyl)arylmethanes†

Shinsuke Tahara,a   Fumitoshi Shibahara,a   Toshifumi Maruyamaa  and  Toshiaki Murai*a  

* Corresponding authors

a Department of Chemistry, Faculty of Engineering, Gifu University, Yanagido, Gifu 501-1193, Japan
E-mail: mtoshi@gifu-u.ac.jp
Fax: +81 58 293 2614
Tel: +81 58 293 2614

Abstract

The treatment of N-thioacyl-1-(2-pyridyl)-1,2-aminoalcohols with iodine and pyridine in THF at room temperature for 30 min leads to the formation of bis(1-imidazo[1,5-a]pyridyl)arylmethanes as green solids in good to high yields.

Graphical abstract: Iodine-mediated cyclization of N-thioacyl-1-(2-pyridyl)-1,2-aminoalcohols and their subsequent condensation leading to the formation of novel bis(1-imidazo[1,5-a]pyridyl)arylmethanes

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B910172A
Article type
Communication
Submitted
22 May 2009
Accepted
23 Sep 2009
First published
13 Oct 2009

Chem. Commun., 2009, 7009-7011

Permissions

Request permissions

Iodine-mediated cyclization of N-thioacyl-1-(2-pyridyl)-1,2-aminoalcohols and their subsequent condensation leading to the formation of novel bis(1-imidazo[1,5-a]pyridyl)arylmethanes

S. Tahara, F. Shibahara, T. Maruyama and T. Murai, Chem. Commun., 2009, 7009 DOI: 10.1039/B910172A

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