Ben Feringa and co-workers at the University of Groningen have reported in ACIE on a palladium catalzyed anti-Markovnikov oxidation of allylic esters. This is the opposite of what we see in a Wacker-Tsuji process.
Archive for the ‘Wacker’ Category
Anti-Markovnikov oxidation of allylic esters
Posted by naturalproductman on April 18, 2013
Posted in Methodology, Named Reactions, Palladium, Transition Metal, Wacker | Leave a Comment »
Fusarisetin A synthesis
Posted by naturalproductman on December 30, 2011
Ang Li and co-workers at Shanghai Institute of Organic Chemistry have reported in JACS on the synthesis of fusarisetin A.
Posted in Asymmetric, Cascade Reactions, Methodology, Named Reactions, Palladium, Transition Metal, Wacker | Leave a Comment »
Enantioselective Wacker Oxidation
Posted by naturalproductman on June 25, 2010
Hiroaki Sasai and co-workers at Osaka University have published in Org Lett on an enantioselective Wacker cyclization using a palladium catalyst with a SPRIX ligand.

Posted in Asymmetric, Cascade Reactions, Methodology, Palladium, Transition Metal, Wacker | Leave a Comment »
