Issue 15, 2005
From the journal:

Chemical Communications

Intramolecular iodoarylation reaction of alkynes: easy access to derivatives of benzofused heterocycles†

José Barluenga,*a   Mónica Trincado,a   María Marco-Arias,a   Alfredo Ballesteros,a   Eduardo Rubioa  and  José M. Gonzáleza  

* Corresponding authors

a Instituto Universitario de Química Organometálica “Enrique Moles”-Unidad Asociada al C.S.I.C., Universidad de Oviedo, C/Julián Clavería, 8, 33006-Oviedo, Spain
E-mail: barluenga@uniovi.es
Fax: +34 985103450
Tel: +34 985103450

Abstract

The iodoarylation reaction of heteroatom-tethered ω-arylalkynes offers an efficient and straightforward entry to heterocycles. As a result, both C–C ring-closing from readily available precursors, and concomitant selective iodination take place. The first related study conducted in water is presented.

Graphical abstract: Intramolecular iodoarylation reaction of alkynes: easy access to derivatives of benzofused heterocycles

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B500303B
Article type
Communication
Submitted
13 Jan 2005
Accepted
04 Feb 2005
First published
22 Feb 2005

Chem. Commun., 2005, 2008-2010

Permissions

Request permissions

Intramolecular iodoarylation reaction of alkynes: easy access to derivatives of benzofused heterocycles

J. Barluenga, M. Trincado, M. Marco-Arias, A. Ballesteros, E. Rubio and J. M. González, Chem. Commun., 2005, 2008 DOI: 10.1039/B500303B

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