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Event Highlights
New Horizons in Catalysis:
The Art of Catalysis in Process Chemistry
12 - 13 April 2007, Barcelona, Spain
Synthetic Heterocyclic Chemistry
Design Syntheses, Develop Processes
12 - 13 April 2007, Barcelona, Spain
Organic Process Research & Development
The Definitive Process Development Conference!
14 - 17 May 2007, Jersey, Channel Islands
ADME and hERG in Medicinal Chemistry
Succeeding Through Literature
17 - 18 April 2007, Edinburgh, UK
The Design, Development and Scale-Up of Safe Chemical Processes and Operations
18 - 20 April 2007, Princeton, New Jersey, USA
Making & Using Fluoroorganic Molecules
19 - 20 April 2007, Florence, Italy
Optical Resolutions: Theory & Practice
23 - 24 April 2007, London, UK
Visit our web site for up to date details and special offers on our forthcoming events >
I was always taught that gold was an unreactive metal and not much use in catalytic reactions. But that was in the sixties. In 1973 Bond (not James! nor anything to do with Goldfinger) reported that a supported gold catalyst could be used in the hydrogenation of olefins and more than 10 years later the groups of Haruta and, independently, Hutchings showed that gold catalysts could be used in the low temperature oxidation of CO and in the hydrochlorination of acetylene to vinyl chloride. For the first time, these studies showed that gold was the preferred catalyst for these reactions and destroyed the myth of the poor activity of gold. This area has become a dynamic hot spot in catalysis research and has resulted in the European Union Research Training Network AURICAT.
A recent review describes exactly how useful gold catalysts can be. The review, written by two of the most active researchers in the field, Prof Hashmi from University of Stuttgart and Prof Hutchins at the University of Cardiff, covers both heterogeneous and homogeneous catalysis. (A S K Hashmi and G J Hutchins, Angew Chem Int Ed, 2006, 45, 7896-7936).
• Trevor Laird
Some interesting transformations are shown in the scheme featured in the full downloadable newsletter.
Most modern chemists wishing to make aromatic tertiary amines will try the Buchwald Hartwig methodologies involving displacement of a halide or other leaving group by an amine under palladium or copper catalysis. more>
The cyanation of aryl halides using palladium catalysis is a powerful and well documented transformation which on the face of it should be quite robust, but in fact still proves problematic in many cases. more>
Taiwanese chemists* have reported simple and mild conditions for the dehydration of primary amides to nitriles, using ethyl chlorophosphate and base: more>
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Most chemists find it hard to keep up with the literature and reading journals often comes at the bottom of the pile (literally with hard-copy journals) when it comes to work priorities. However for a chemist to be truly innovative it is vitally important to know the latest advances in the subject. more>
The periodic table as you have never seen it before!
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