Using Transition Metal Catalysis to Achieve New Reactivity and Selectivity for Organic Synthesis
Lead Research Organisation:
University of Oxford
Department Name: Oxford Chemistry
Abstract
The ability to build molecules is crucial to molecular science. For new synthetic methods to be accepted as useful tools a demanding set of criteria need to be satisfied; advantages of cost, environmental impact, operational simplicity and reaction efficiency are some of the most important factors to be considered. The focus of this fellowship is to develop new methods to prepare molecules using tools based on transition metal catalysts.The unique reactivities presented by transition metals make them attractive reagents to explore, and to tackle several of the issues discussed above. In particular we plan to use transition metal catalysts to allow the conversion of readily available organic molecules into high value functionalised molecules useful for further manipulation. One of the key aims is to achieve these reactions in a highly selective manner, delivering only single products when the formation of mixtures of several related molecules is possible. We also plan to deliver methods that are easy to perform and that require no special handling techniques.
Organisations
People |
ORCID iD |
Michael Willis (Principal Investigator) |
Publications
Byrne SJ
(2010)
Enantioselective desymmetrizing palladium catalyzed carbonylation reactions: the catalytic asymmetric synthesis of quaternary carbon center containing 1,3-dienes.
in Organic & biomolecular chemistry
Durbin MJ
(2008)
Palladium-catalyzed alpha-arylation of oxindoles.
in Organic letters
González-Rodríguez C
(2010)
Rhodium-catalysed intermolecular alkyne hydroacylation: the enantioselective synthesis of a- and ß-substituted ketones by kinetic resolution.
in Chemistry (Weinheim an der Bergstrasse, Germany)
Hodgkinson R
(2009)
Palladium-catalysed tandem alkenyl- and aryl-C-N bond formation: a cascade N-annulation route to 1-functionalised 7-azaindoles
in Tetrahedron
Moxham GL
(2008)
Intermolecular alkene and alkyne hydroacylation with beta-S-substituted aldehydes: mechanistic insight into the role of a hemilabile P-O-P ligand.
in Chemistry (Weinheim an der Bergstrasse, Germany)
Pawley R
(2010)
Controlling Selectivity in Intermolecular Alkene or Aldehyde Hydroacylation Reactions Catalyzed by {Rh(L 2 )} + Fragments
in Organometallics
Stainforth N
(2009)
Direct catalytic diastereoselective Mannich reactions: the synthesis of protected a-hydroxy-ß-aminoketones
in Tetrahedron: Asymmetry
Tadd AC
(2009)
Palladium-catalyzed aryl halide carbonylation-intramolecular O-enolate acylation: efficient isocoumarin synthesis, including the synthesis of thunberginol A.
in Chemical communications (Cambridge, England)
Willis MC
(2010)
Transition metal catalyzed alkene and alkyne hydroacylation.
in Chemical reviews
Yagoubi M
(2010)
Cascade palladium-catalyzed direct intramolecular arylation/alkene isomerization sequences: synthesis of indoles and benzofurans.
in Angewandte Chemie (International ed. in English)