Issue 3, 2016

Combining photochemistry and catalysis: rapid access to sp3 – rich polyheterocycles from simple pyrroles

Abstract

Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tricyclic aziridines. These undergo a range of novel palladium-catalyzed ring-opening and cycloaddition reactions, likely driven by their inherent strain, allowing incorporation of further functionality by fusing additional heterocyclic rings onto these already complex polycyclic cores. This rapid, 2-step access to complex sp3 – rich heterocycles should be of interest to those in the fields of drug discovery and natural product synthesis.

Graphical abstract: Combining photochemistry and catalysis: rapid access to sp3 – rich polyheterocycles from simple pyrroles

Supplementary files

Article information

Article type
Edge Article
Submitted
26 Oct 2015
Accepted
30 Dec 2015
First published
04 Jan 2016
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2016,7, 2302-2307

Author version available

Combining photochemistry and catalysis: rapid access to sp3 – rich polyheterocycles from simple pyrroles

E. E. Blackham, J. P. Knowles, J. Burgess and K. I. Booker-Milburn, Chem. Sci., 2016, 7, 2302 DOI: 10.1039/C5SC04062K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements