Archive for the ‘Cooperative Catalysis’ Category
Posted by naturalproductman on February 10, 2012
Masahiro Terada and co-worker from Tohoku University have reported in ACIEE on a relay catalysis

ACIEE paper
Posted in Cooperative Catalysis, Methodology, Organocatalytic, Rhodium, Transition Metal | Leave a Comment »
Posted by naturalproductman on September 23, 2011
Yong-Gui Zhou and co-workers at the Chinese Academy of Sciences have reported in JACS on a reduction of benzoxazinones using Hantzsch esters and ruthenium to regenerate the reduced form of the Hantzsch esters.

JACS paper
Posted in Asymmetric, Cascade Reactions, Cooperative Catalysis, Methodology, Organocatalytic, Ruthenium, Transition Metal | Leave a Comment »
Posted by naturalproductman on September 19, 2011
Abigail Doyle and colleague have reported in JACS on an epoxide ring opening reaction using a fluoride group.

JACS Paper
Posted in Cobalt, Cooperative Catalysis, Methodology, Ring Opening, Transition Metal | Leave a Comment »
Posted by naturalproductman on May 17, 2011
Shunsuke Chiba and co-workers at Nanyang Technological University in Singapore have reported in ACIEE on a copper and rhodium catalyzed cyclization of a vinyl azide and an alkyne.

ACIEE paper
Posted in Cascade Reactions, Cooperative Catalysis, Copper, Methodology, Rhodium, Ring forming, Transition Metal | Leave a Comment »
Posted by naturalproductman on March 9, 2011
Yoshiaki Nishibayashi and co-workers at the University of Tokyo have reported in European Journal of Organic Chemistry on a cooperative catalysis example.

European JOC paper
Posted in Cooperative Catalysis, Iron, Methodology, Organocatalytic, Transition Metal | Leave a Comment »
Posted by naturalproductman on February 6, 2011
Clement Mazet and co-workers at the Universite Geneve have published in ACIEE on a sequential iridium catalyzed isomerization of an allylic alcohol to an aldehyde followed by enamine catalysis to form an alpha-substituted aldehyde.

ACIEE paper
Posted in Cooperative Catalysis, Iridium, Methodology, Transition Metal | Leave a Comment »
Posted by naturalproductman on January 11, 2011
Yoshiaki Nishibayashi and co-workers from the University of Tokyo have published in Organic Letters on a cooperative catalysis approach to add a propargylic group onto the alpha position of an aldehyde.

OL paper
Posted in Asymmetric, Cascade Reactions, Cooperative Catalysis, Copper, Methodology, Transition Metal | Leave a Comment »
Posted by naturalproductman on July 23, 2010
Junliang Xiao and co-workers from the University of Liverpool have published in Organic Letters on a cooperative catalysis approach to acylate aryl chlorides by combining aldehydes with corresponding aryl chlorides using palladium and pyrrolidine.

OL paper
Posted in Cooperative Catalysis, Methodology, Organocatalytic, Palladium, Transition Metal | Leave a Comment »
Posted by naturalproductman on July 14, 2010
Yoshiaki Nishibayashi and co-workers at the University of Tokyo have published in ACIEE on a cooperative catalysis approach to combining a propargylic alcohol with an aldehyde.

ACIEE paper
Posted in Cooperative Catalysis, Methodology, Organocatalytic, Ruthenium, Transition Metal | Leave a Comment »
Posted by naturalproductman on May 12, 2010
Virginie Ratovelomanana-Vidal and co-workers at Chimie ParisTech have published in Organic Letters on what looks like an indium promoted Conia-Ene cyclization.

OL paper
Posted in Cascade Reactions, Conia-Ene, Cooperative Catalysis, Methodology, Named Reactions, Ring forming | Leave a Comment »