Issue 22, 2011

The photo-dehydro-Diels–Alder (PDDA) reaction

Abstract

The photo-dehydro-Diels–Alder (PDDA) reaction is a valuable extension of the classical Diels–Alder (DA) reaction. The PDDA reaction differs from the DA reaction by the replacement of one of the C–C-double bonds of the diene moiety by a C–C triple bond and by the photochemical triggering of the reaction. This entails that, in contrast to the DA reaction, the PDDA reaction proceeds according to a multistage mechanism with biradicals and cycloallenes as intermediates. The PDDA reaction provides access to a considerable variety of compound classes. For example, 1-phenylnaphthlenes, 1,1′-binaphthyls, N-heterocyclic biaryls, and naphthalenophanes could be obtained by this reaction.

Graphical abstract: The photo-dehydro-Diels–Alder (PDDA) reaction

Article information

Article type
Emerging Area
Submitted
02 Jul 2011
Accepted
09 Aug 2011
First published
10 Aug 2011

Org. Biomol. Chem., 2011,9, 7599-7605

The photo-dehydro-Diels–Alder (PDDA) reaction

P. Wessig, A. Matthes and C. Pick, Org. Biomol. Chem., 2011, 9, 7599 DOI: 10.1039/C1OB06066J

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