Archive for the ‘Mizoroki-Heck’ Category
Posted by naturalproductman on October 25, 2012
Janine Cossy and co-workers from CNRS have reported in Organic Letters on a palladium catalyzed approach to access trienols.

OL paper
Posted in cross coupling, Methodology, Mizoroki-Heck, Palladium, Transition Metal | Leave a Comment »
Posted by naturalproductman on June 23, 2010
Matthias Beller and co-workers at Leibniz-Institut für Katalyse e.V. Albert-Einstein-Strasse have published in ACIEE on a palladium catalyzed carbonylative Heck reaction.

ACIEE paper
Posted in Cascade Reactions, cross coupling, Methodology, Mizoroki-Heck, Multi-Component Coupling | Leave a Comment »
Posted by naturalproductman on June 21, 2010
Masahiro Hirama and co-workers at Tohoku University have published in the European Journal of Organic Chemistry on the synthesis of lycodine.

European JOC paper
Posted in Alkaloids, Cascade Reactions, cross coupling, Cycloaddition, Diels-Alder, Methodology, Mizoroki-Heck, Named Reactions, Palladium, Pericyclic reactions, Transition Metal | Leave a Comment »
Posted by naturalproductman on May 20, 2010
Mark Lautens and co-worker at the University of Toronto have published in Organic Letters on the use of a gem-dibromoalkene to form an indene ring and a new C-C bond via an intermolecular Suzuki/Heck reaction. Usually we see alkynes as precursors to these transition metal catalyzed indene formations, but this dibromo-olefin is another approach.

OL paper
Posted in cross coupling, Methodology, Mizoroki-Heck, Palladium, Ring forming, Suzuki-Miyaura, Transition Metal | Leave a Comment »
Posted by naturalproductman on May 5, 2010
John Wolfe and co-workers from the University of Michigan have recently reported in Organic Letters on a carboamination process involving a palladium catalyst.

OL paper
Posted in Cascade Reactions, cross coupling, Methodology, Mizoroki-Heck, Palladium, Transition Metal | Leave a Comment »
Posted by naturalproductman on March 25, 2010
Naoto Chatani and co-workers from Osaka University have recently reported in Organic Letters on a rhodium catalyzed C-C cleavage of an aryl cyanide substrate and coupled the aryl unit to an sp2-carbon.

OL paper
Posted in C-C Bond Breaking, cross coupling, Heck, Methodology, Mizoroki-Heck, Rhodium, Transition Metal | Leave a Comment »