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 ‘Palladium’ 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 »
Chiral allene synthesis
Posted by naturalproductman on March 20, 2013
Doug Frantz and co-workers at UT San Antonio have reported in JACS on a palladium catalyzed asymmetric approach to synthesizing axially chiral allenes through beta-hydride elimination.

Posted in Allenes, Asymmetric, Methodology, Palladium, Transition Metal | Leave a Comment »
Pd-catalyzed 3 component coupling
Posted by naturalproductman on March 13, 2013
Matthew Sigman and colleague at the University of Utah have reported in JACS on a palladium catalyzed three component coupling reaction.

Posted in Cascade Reactions, Methodology, Multi-Component Coupling, Palladium, Transition Metal | Leave a Comment »
Aminopalladation
Posted by naturalproductman on February 26, 2013
Jieping Zhu and co-workers from CNRS have reported in Tetrahedron on an aminopalladation reaction.

Posted in Cascade Reactions, Methodology, Palladium, Transition Metal | Leave a Comment »
Spontaneous Diels-Alder
Posted by naturalproductman on January 31, 2013
Craig Merlic and co-workers from UCLA have reported in Organic Letters on a spontaneous transannular Diels-Alder when they used a palladium catalyzed C-C bond forming strategy.

Posted in Cascade Reactions, Diels-Alder, Methodology, Named Reactions, Palladium, Transition Metal | Leave a Comment »
Allylation
Posted by naturalproductman on January 31, 2013
David Lupton and colleague from Monash University have reported in ACIE on a Tsuji-Trost approach for the synthesis of (−)-Kopsihainanine A.

Posted in Alkaloids, Asymmetric, Methodology, Named Reactions, Palladium, Transition Metal, Tsuji-Trost | Leave a Comment »
pyridines from allenes
Posted by naturalproductman on December 29, 2012
Andrei Yudin and co-workers from the University of Toronto have reported in OL on the synthesis of pyridines from allenes.

Posted in Allenes, Methodology, Palladium, Transition Metal | Leave a Comment »
C-H arylation of cyclopropanes
Posted by naturalproductman on November 19, 2012
Nicolai Cramer and co-worker from ETH Zurich have reported in ACIE on a C-H arylation of cyclopropanes.

Posted in C-H activation, Methodology, Palladium, Ring expansion, Transition Metal | Leave a Comment »
Paspalinine synthesis
Posted by naturalproductman on November 16, 2012
Shigefumi Kuwahara and co-workers from Tohoku University have reported in ACIE on the synthesis of paspalinine.
Posted in Alkaloids, Cascade Reactions, Indoles, Methodology, Palladium, Total Synthesis, Transition Metal | Leave a Comment »
Aromatization with palladium
Posted by naturalproductman on October 25, 2012
Naohiko Yoshikai and co-workers from Nanyang Technological University have reported in Organic Letters on the conversion of cyclohexanone to anlines using palladium and 1 atmosphere of oxygen.

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

