Issue 82, 2012
From the journal:

Chemical Communications

Enantioselectivity in visible light-induced, singlet oxygen [2+4] cycloaddition reactions (type II photooxygenations) of 2-pyridones†

Christian Wiegand,a   Eberhardt Herdtwecka  and  Thorsten Bach*a  

* Corresponding authors

a Department Chemie and Catalysis Research Center (CRC), Technische Universität München, 85747 Garching, Germany
E-mail: thorsten.bach@ch.tum.de
Fax: +49 89 28913315
Tel: +49 89 28913330

Abstract

3-Substituted 2-pyridones were enantioselectively (68–90% ee) converted into the respective 3-hydroxypyridine-2,6-diones by a sequence consisting of a template-mediated type II photooxygenation and an acid-catalysed rearrangement.

Graphical abstract: Enantioselectivity in visible light-induced, singlet oxygen [2+4] cycloaddition reactions (type II photooxygenations) of 2-pyridones

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C2CC35621J
Article type
Communication
Submitted
02 Aug 2012
Accepted
22 Aug 2012
First published
10 Sep 2012

Chem. Commun., 2012,48, 10195-10197

Permissions

Request permissions

Enantioselectivity in visible light-induced, singlet oxygen [2+4] cycloaddition reactions (type II photooxygenations) of 2-pyridones

C. Wiegand, E. Herdtweck and T. Bach, Chem. Commun., 2012, 48, 10195 DOI: 10.1039/C2CC35621J

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