NHC Ligands and Complexes

N-{[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]methyl}-N-cyclopropylamine.

Ondansetron Impurity B is a dimeric impurity of the 5-HT|3|receptor antagonist Ondansetron (sc-201127). Ondansetron Impurity B, potentially isolated from the synthesis of Ondansetron, is formed by the dimerization of two Ondansetron molecules

2-phenyl-4, 4, 5, 5,-tetramethylimidazoline-1-oxyl 3-oxide (PTIO) has been used as a nitric oxide (NO) scavenger.

2-phenyl-4, 4, 5, 5,-tetramethylimidazoline-1-oxyl 3-oxide (PTIO) has been used as a nitric oxide (NO) scavenger.

Catalytic oxidant for copper-catalyzed, greener oxidation of alcohols under aerobic conditions. Copper(I)/TEMPO-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air. TEMPO (2,2,6,6-Tetramethyl-1-piperidinyloxy) was used for

Catalytic oxidant for copper-catalyzed, greener oxidation of alcohols under aerobic conditions. Copper(I)/TEMPO-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air. TEMPO (2,2,6,6-Tetramethyl-1-piperidinyloxy) was used for

Catalytic oxidant for copper-catalyzed, greener oxidation of alcohols under aerobic conditions. Copper(I)/TEMPO-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air. TEMPO (2,2,6,6-Tetramethyl-1-piperidinyloxy) was used for

Catalytic oxidant for copper-catalyzed, greener oxidation of alcohols under aerobic conditions. Copper(I)/TEMPO-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air. TEMPO (2,2,6,6-Tetramethyl-1-piperidinyloxy) was used for

Catalytic oxidant for copper-catalyzed, greener oxidation of alcohols under aerobic conditions. Copper(I)/TEMPO-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air. TEMPO (2,2,6,6-Tetramethyl-1-piperidinyloxy) was used for

tert-butyl 1-(hydroxymethyl)-3-azabicyclo[3.1.1]heptane-3-carboxylate.

tert-butyl 1-(hydroxymethyl)-3-azabicyclo[3.1.1]heptane-3-carboxylate.

tert-butyl 6-oxo-2-azabicyclo[2.2.1]heptane-2-carboxylate.