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Palladium‐Catalyzed Substitution of Allylic Fluorides
Authors:Amaruka Hazari  Véronique Gouverneur Prof.  John M. Brown Dr.
Affiliation:Chemistry Research Laboratory, Oxford University, 12 Mansfield Rd., Oxford OX1?3TA (UK), Fax: (+44)?1865‐285‐002 http://www.chem.ox.ac.uk/researchguide/vgouverneur.htmlhttp://www.chem.ox.ac.uk/researchguide/jbrown.html
Abstract:
As unusual substrates for the Tsuji–Trost allylation reaction, allylic fluorides are responsive to palladium‐catalyzed substitution. Their activity towards this reaction fits in the series OCO2Me>OBz? F ?OAc. The classic stereoretention mechanism that involves sequential inversions does not operate in this case. Several distinct cases are considered.
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Keywords:allyl ligands  allylation  homogeneous catalysis  palladium  reaction mechanisms
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