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SUMMARY:Palladium-Catalyzed Reactions Using Strained Tertiary Alcohols
DTSTART:20140903T171500
DTEND:20140903T181500
DTSTAMP:20260408T000114Z
UID:b515e4ba465f11ff32f9ee98c9dbaf3b965bdd3846ae194d76c73762
CATEGORIES:Conferences - Seminars
DESCRIPTION:Professor Arturo Orellana\, University of York\, Toronto\, Can
 ada\nOver the last 30 years the development of palladium-catalyzed reactio
 ns has revolutionized the way we conduct synthesis\, and there are many ca
 rbon-carbon bond forming processes\, such as the Suzuki-Miyaura reaction\,
  that are now routine. The rich chemistry of palladium\, however\, still o
 ffers many opportunities for the development of new reactions and strategi
 es for synthesis. We have been concerned with the development of palladium
 -catalyzed reactions using tertiary alcohols\, substrates that are conside
 red to be either too unstable or too inert for use as cross-coupling partn
 ers. In this talk I will present our recent progress on the use of these 
 ‘neglected substrates’ in new strategies for carbon-carbon bond format
 ion.
LOCATION:BCH 2218 https://plan.epfl.ch/?room==BCH%202218
STATUS:CONFIRMED
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