Carbon-carbon bond-forming reductive elimination from elusive organocopper(III) complexes has been considered the key step in many copper-catalyzed and organocuprate reactions. However, organocopper(III) complexes with well-defined structures that can undergo reductive elimination are extremely rare, especially for the formation of Csp 3-Csp 3 bonds. We report herein a general method for the synthesis of a series [alkyl-Cu III-(CF 3) 3 ]complexes, the structures of which have been unequivocally characterized by NMR, mass spectrometry and X-ray crystal diffraction. At elevated temperature, these complexes undergo reductive elimination following first-order kinetics, forming alky-CF 3 products with good yields (up to 91%). Both Kinetic studies and DFT calculations indicate that the reductive elimination to form Csp 3-CF 3 bonds proceeds through a concerted transition state, with a ΔH ‡ =20 kcal/mol barrier.
Capped chelating organic molecules are presented as a design principle for tuning heterogeneous nanoparticles for electrochemical catalysis. Gold nanoparticles (AuNPs) functionalized with a chelating tetradentate porphyrin ligand show a 110-fold enhancement compared to the oleylamine-coated AuNP in current density for electrochemical reduction of CO to CO in water at an overpotential of 340 mV with Faradaic efficiencies (FEs) of 93 %. These catalysts also show excellent stability without deactivation (<5 % productivity loss) within 72 hours of electrolysis. DFT calculation results further confirm the chelation effect in stabilizing molecule/NP interface and tailoring catalytic activity. This general approach is thus anticipated to be complementary to current NP catalyst design approaches.
Trifluoromethyl-containing compounds play a significant role in medicinal chemistry, materials and fine chemistry. Although direct C-H trifluoromethylation has been achieved on Csp -H bonds, direct conversion of Csp -H bonds to Csp -CF remains challenging. We report herein an efficient protocol for the selective trifluoromethylation of benzylic C-H bonds. This process is mediated by a combination Cu -CF species and persulfate salts. A wide range of methylarenes can be selectively trifluoromethylated at the benzylic positions. A combination of experimental and theoretical mechanistic studies suggests that the reaction involves a radical intermediate and a Cu -CF species as the CF transfer reagent.
Capped chelating organic molecules are presented as a design principle for tuning heterogeneous nanoparticles for electrochemical catalysis. Gold nanoparticles (AuNPs) functionalized with a chelating tetradentate porphyrin ligand show a 110‐fold enhancement compared to the oleylamine‐coated AuNP in current density for electrochemical reduction of CO2 to CO in water at an overpotential of 340 mV with Faradaic efficiencies (FEs) of 93 %. These catalysts also show excellent stability without deactivation (<5 % productivity loss) within 72 hours of electrolysis. DFT calculation results further confirm the chelation effect in stabilizing molecule/NP interface and tailoring catalytic activity. This general approach is thus anticipated to be complementary to current NP catalyst design approaches.
Herein, we present a strategy for the preparation of
3′-fluorinated
nucleoside analogues via the aminocatalytic, electrophilic
fluorination of readily accessible and bench-stable 2′-ketonucleosides.
Initially developed to facilitate the manufacture of 3′-fluoroguanosine
(3′-FG)a substructure of anticancer therapeutic MK-1454this
strategy has been extended to the synthesis of a variety of 3′-fluoronucleosides.
Finally, we demonstrate the utility of the 2′-ketonucleoside
synthon as a platform for further diversification and suggest that
this methodology should be broadly applicable to the discovery of
novel nucleoside analogues.
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