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It has long been known that catalysts not only speed up chemical transformations, but can also make reactions occur in ways that would otherwise be impossible. Similarly, the ability to manipulate reactions to obtain just one product when many others are likely to form is a long-standing goal of synthetic chemists. Ohshima and colleagues¡¯ work1 thus
represents a real advance in nucleophilic reactions. But it also reminds chemists to challenge their assumptions about the relative reactivity
of the chemical groups in organic molecules.Such assumptions may be the biggest barrier to the discovery of exciting new reactions.


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2008 Proline-catalysed Mannich reactions of acetaldehyde.pdf (201.34 KB)
2008 Proline-catalysed Mannich reactions of acetaldehyde.pdf (201.34 KB)



Proline-catalysed Mannich reactions of acetaldehyde p453

Jung Woon Yang, Carley Chandler, Michael Stadler, Daniela Kampen & Benjamin List

doi:10.1038/nature06740

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The Roles of Subsurface Carbon and Hydrogen in Palladium-Catalyzed
The Roles of Subsurface Carbon and Hydrogen in Palladium-Catalyzed Alkyne Hydrogenation
Detre Teschner, J¨¢nos Borsodi, Attila Wootsch, Zsolt R¨¦vay, Michael Hävecker, Axel Knop-Gericke, S. David Jackson, and Robert Schlögl
Science 4 April 2008: 86-89.
The population of hydrogen and carbon within a palladium catalyst governs the hydrogenation of alkynes on its surface.
http://www.chemj.cn/viewthread.php?tid=1278&extra=page%3D1
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