Sigma-Aldrich

Application This ligand was developed by the Yu lab to enable the Pd-catalyzed dehydrogenation of aliphatic carboxylic acids through a typically challenging activation of the &#946-methylene C-H bond. This method is chemoselective to carboxylic

Application This ligand was developed by the Yu lab to enable the Pd-catalyzed dehydrogenation of aliphatic carboxylic acids through a typically challenging activation of the &#946-methylene C-H bond. This method is chemoselective to carboxylic

Application This ligand was developed by the Yu lab to enable the Pd-catalyzed dehydrogenation of aliphatic carboxylic acids through a typically challenging activation of the &#946-methylene C-H bond. This method is chemoselective to carboxylic

Application This ligand was developed by the Yu lab to enable the Pd-catalyzed dehydrogenation of aliphatic carboxylic acids through a typically challenging activation of the &#946-methylene C-H bond. This method is chemoselective to carboxylic

Application 1,4-Diethyl 2-(1-pyridin-1-ium-yl)butanedioate ethylsulfate is a bench-stable pyridinium feedstock capable of acting as an inexpensive, scalable and practical building block toward the synthesis of a variety of C-4 alkyl pyridines.

Application 1,4-Diethyl 2-(1-pyridin-1-ium-yl)butanedioate ethylsulfate is a bench-stable pyridinium feedstock capable of acting as an inexpensive, scalable and practical building block toward the synthesis of a variety of C-4 alkyl pyridines.

Application PSI 2 is a stable and sustainably prepared P(V) reagent developed by the Baran Lab for the synthesis of phosphorodithioate oligonucleotides. The phosphorodithioate linkages afforded by PSI 2 are effectively cleaved by RNAse-H while

Application PSI 2 is a stable and sustainably prepared P(V) reagent developed by the Baran Lab for the synthesis of phosphorodithioate oligonucleotides. The phosphorodithioate linkages afforded by PSI 2 are effectively cleaved by RNAse-H while

Application PSI 2 is a stable and sustainably prepared P(V) reagent developed by the Baran Lab for the synthesis of phosphorodithioate oligonucleotides. The phosphorodithioate linkages afforded by PSI 2 are effectively cleaved by RNAse-H while

Application This chiral acetyl-protected aminoethyl quinoline (APAQ) ligand was developed by the Yu group for ligand-enabled acceleration of Pd-catalyzed enantioselective &#946-methylene C–H functionalization, which is important for the

Application Powerful guanidinylation reagent from the Baran Lab developed for the installation of monoprotected boc-guanidine on primary and secondary amines, particularly electron-deficient and hindered amines . Other Notes 11-Step Total Synthesis

Application Pyridin-3-yl sulfurofluoridate can be used in the Pd-catalyzed Suzuki-Miyuara cross-coupling reaction. The fluorosulfate functionality was shown by Sharpless and coworkers to have distinct reactivity in comparison to other functional