Archive for the ‘cross coupling’ Category
Metal Catalyzed Cross Coupling Reactions
Posted by naturalproductman on April 2, 2013
Dirk Trauner and co-workers at have reported in Organic Letters on a Stille-Diels Alder cascade approach towards PF-1018.

OL paper
Posted in Cascade Reactions, cross coupling, Diels-Alder, Methodology, Named Reactions, Stille | Leave a Comment »
Posted by naturalproductman on November 2, 2012
I guess Greg Fu made a statement at Caltech with his Science paper in collaboration with the Jonas Peters group. This Science paper discloses an Ullman reaction (copper mediated aryl iodide and amine coupling) in the presence of light.
Science paper
Posted in Copper, cross coupling, Light Mediated, Methodology, Transition Metal, Ullmann | Leave a Comment »
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 21, 2012
Susumu Kobayashi and co-workers at the Tokyo University of Science have reported in ACIE on the synthesis of myxalamide.

ACIE paper
Posted in Alkaloids, cross coupling, Methodology, Polyenes | Leave a Comment »
Posted by naturalproductman on June 11, 2012
Silas Cook and colleague at Indiana University have reported in Organic Letters on a formal synthesis of englerin.

OL paper
Posted in cross coupling, Heck, Methodology, Sesquiterpenoids, Seven-Membered Rings | Leave a Comment »
Posted by naturalproductman on March 29, 2012
The Nozaki-Hiyama-Kishi coupling couples an a R-halide group with an aldehyde. Kishi and co-workers have reported on a catalytic, asymmetric version in JACS recently.

JACS paper
Posted in Asymmetric, Chromium, cross coupling, Methodology, Named Reactions, Nickel, Nozaki-Hiyama-Kishi, Transition Metal | Leave a Comment »
Posted by naturalproductman on February 23, 2012
Qian Cai and co-workers from Guanzhou Institutes of Biomedicine and Health have reported in Organic Letters on a click reaction followed by cross coupling.

OL paper
Posted in Cascade Reactions, Copper, cross coupling, Methodology, Transition Metal | 2 Comments »
Posted by naturalproductman on February 21, 2012
Buchwald and co-workers have reported in ACIEE on an iron catalyzed trifluoromethylation of vinyltrifluoroborates.

ACIEE paper
Posted in Cascade Reactions, cross coupling, Iron, Methodology, Transition Metal | Leave a Comment »
Posted by naturalproductman on December 5, 2011
Michinori Suginome and co-workers at Kyoto University have published in JACS on the enantiospecificity of a Suzuki-Miyaura reaction and they show that inversion or retention can occur depending on the additive.

JACS paper
Posted in Asymmetric, cross coupling, Methodology, Palladium, Suzuki-Miyaura, Transition Metal, Zirconium | Leave a Comment »
Posted by naturalproductman on December 2, 2011
Shane Krska and colleague at Merck have reported in JACS on a way to form ketones from acyl silanes using a palladium catalyst.

JACS paper
Posted in Cascade Reactions, cross coupling, Methodology, Palladium, Transition Metal | Leave a Comment »