In Pd-catalyzed C[BOND]N cross-coupling reactions, α-branched secondary amines are difficult coupling partners and the desired products are often produced in low yields. In order to provide a robust method for accessing N-aryl α-branched tertiary amines, new catalysts have been designed to suppress undesired side reactions often encountered when these amine nucleophiles are used. These advances enabled the arylation of a wide array of sterically encumbered amines, highlighting the importance of rational ligand design in facilitating challenging Pd-catalyzed cross-coupling reactions.National Institutes of Health (U.S.) (Grant GM58160)National Science Foundation (U.S.). Graduate Research Fellowship Progra
L,X-Type transient directing groups (TDGs) based on a reversible imine linkage have emerged as broad...
We report the efficient N-arylation of acyclic secondary amides and related nucleophiles with aryl n...
Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1999.Includes bibliograph...
We report the Pd-catalyzed arylation of very hindered α,α,α-trisubstituted primary amines. Kinetics-...
Thesis: Ph. D. in Organic Chemistry, Massachusetts Institute of Technology, Department of Chemistry,...
Copyright © 2020 American Chemical Society. We have developed a new dialkylbiaryl monophosphine liga...
We report the Pd-catalyzed arylation of very hindered α,α,α-trisubstituted primary amines. Kinetics-...
We report the Pd-catalyzed arylation of very hindered α,α,α-trisubstituted primary amines. Kinetics-...
1 v. (various pagings) : ill. ; 30 cm.PolyU Library Call No.: [THS] LG51 .H577M ABCT 2012 ChungPalla...
There have been numerous developments in C–H activation reactions in the past decade. Attracted by t...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...
Palladium-catalyzed cross-coupling reactions between C–X/C–H bonds and nucleophilic reagents remain ...
We report our studies on the use of two catalyst systems, based on the ligands BrettPhos and RuPhos,...
International audienceThe palladium-catalyzed ligand-controlled arylation of α-zincated acyclic amin...
Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1999.Includes bibliograph...
L,X-Type transient directing groups (TDGs) based on a reversible imine linkage have emerged as broad...
We report the efficient N-arylation of acyclic secondary amides and related nucleophiles with aryl n...
Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1999.Includes bibliograph...
We report the Pd-catalyzed arylation of very hindered α,α,α-trisubstituted primary amines. Kinetics-...
Thesis: Ph. D. in Organic Chemistry, Massachusetts Institute of Technology, Department of Chemistry,...
Copyright © 2020 American Chemical Society. We have developed a new dialkylbiaryl monophosphine liga...
We report the Pd-catalyzed arylation of very hindered α,α,α-trisubstituted primary amines. Kinetics-...
We report the Pd-catalyzed arylation of very hindered α,α,α-trisubstituted primary amines. Kinetics-...
1 v. (various pagings) : ill. ; 30 cm.PolyU Library Call No.: [THS] LG51 .H577M ABCT 2012 ChungPalla...
There have been numerous developments in C–H activation reactions in the past decade. Attracted by t...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...
Palladium-catalyzed cross-coupling reactions between C–X/C–H bonds and nucleophilic reagents remain ...
We report our studies on the use of two catalyst systems, based on the ligands BrettPhos and RuPhos,...
International audienceThe palladium-catalyzed ligand-controlled arylation of α-zincated acyclic amin...
Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1999.Includes bibliograph...
L,X-Type transient directing groups (TDGs) based on a reversible imine linkage have emerged as broad...
We report the efficient N-arylation of acyclic secondary amides and related nucleophiles with aryl n...
Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1999.Includes bibliograph...