Issue 4, 2012
From the journal:

Organic & Biomolecular Chemistry

2,3-Unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines†

Viktor O. Iaroshenko,*ab   Satenik Mkrtchyan,a   Ashot Gevorgyan,ac   Mariia Miliutina,a   Alexander Villinger,a   Dmytro Volochnyuk,d   Vyacheslav Ya. Sosnovskikhe  and  Peter Langer*af  

* Corresponding authors

a Institut für Chemie, Universität Rostock, Albert-Einstein-Str., 3a, Rostock, Germany
E-mail: viktor.iaroshenko@uni-rostock.de, iva108@googlemail.com
Fax: 00 49 381 49864112
Tel: 0049 381 4986410

b National Taras Shevchenko University, 62 Volodymyrska St., Kyiv-33, Ukraine
E-mail: iva108@googlemail.com

c Faculty of Chemistry, Yerevan State University, Alex Manoogian 1, Yerevan, Armenia

d “Enamine Ltd.” 23 A. Matrosova St., Kyiv, Ukraine

e Department of Chemistry, Ural State University, Ekaterinburg, Russian Federation

f Leibniz-Institut für Katalyse, Van der Universität Rostock, Albert-Einstein-Str. 29a, Rostock, Germany

Abstract

A divergent and regioselective approach to fused pyridines was developed through formal [3 + 3] cyclocondensations from simple 2,3-unsubstituted chromones or their enaminone precursors.

Graphical abstract: 2,3-Unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C1OB06494K
Article type
Paper
Submitted
31 Aug 2011
Accepted
27 Oct 2011
First published
27 Oct 2011

Org. Biomol. Chem., 2012,10, 890-894

Permissions

Request permissions

2,3-Unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines

V. O. Iaroshenko, S. Mkrtchyan, A. Gevorgyan, M. Miliutina, A. Villinger, D. Volochnyuk, V. Ya. Sosnovskikh and P. Langer, Org. Biomol. Chem., 2012, 10, 890 DOI: 10.1039/C1OB06494K

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