Amanote Research
Register
Sign In
Late-Stage Diversification of Imidazole-Based Pharmaceuticals Through Pd-Catalyzed Regioselective CH Bond Arylations
doi 10.1021/acs.joc.9b01469.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Late-Stage Diversification of Imidazole-Based Pharmaceuticals Through Pd-Catalyzed Regioselective CH Bond Arylations
Late-Stage Diversification of Imidazole-Based Pharmaceuticals Through Pd-Catalyzed Regioselective CH Bond Arylations
Palladium-Catalyzed Regioselective C–H Bond Arylations at the C3 Position of Ortho-Substituted Fluorobenzenes
Organic and Biomolecular Chemistry
Organic Chemistry
Theoretical Chemistry
Biochemistry
Physical
Late-Stage Diversification of Biologically Active Molecules via Chemoenzymatic CH Functionalization
Site-Selective Ruthenium-Catalyzed CH Bond Arylations With Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group
Site-Selective Ruthenium-Catalyzed CH Bond Arylations With Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group
Site-Selective Ruthenium-Catalyzed CH Bond Arylations With Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group
Site-Selective Ruthenium-Catalyzed CH Bond Arylations With Boronic Acids: Exploiting Isoindolinones as a Weak Directing Group
Regioselective Pd-Catalyzed Direct C1- And C2-Arylations of Lilolidine for the Access to 5,6-Dihydropyrrolo[3,2,1-Ij]quinoline Derivatives
Beilstein Journal of Organic Chemistry
Organic Chemistry