High-valent copper-nitrene intermediates have long been proposed to play a role in copper-catalyzed aziridination and amination reactions. However, such intermediates have eluded detection for decades, preventing the unambiguous assignments of mechanisms. Moreover, the electronic structure of the proposed copper-nitrene intermediates has also been controversially discussed in the literature. These mechanistic questions and controversy have provided tremendous motivation to probe the accessibility and reactivity of Cu(III)-NR/Cu(II)N(•)R species. In this paper, we report a breakthrough in this field that was achieved by trapping a transient copper-tosylnitrene species, 3-Sc, in the presence of scandium triflate. The sufficient stability of 3-Sc at -90 °C enabled its characterization with optical, resonance Raman, NMR, and X-ray absorption near-edge spectroscopies, which helped to establish its electronic structure as Cu(II)N(•)Ts (Ts = tosyl group) and not Cu(III)NTs. 3-Sc can initiate tosylamination of cyclohexane, thereby suggesting Cu(II)N(•)Ts cores as viable reactants in oxidation catalysis.
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http://dx.doi.org/10.1021/ja306674h | DOI Listing |
Org Lett
May 2024
Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan.
Aerobic oxidative dimerization of hydroxystilbenoids is described. A Cr-salen complex catalyzed the dimerization of hydroxystilbenoids in 1,1,1,3,3,3-hexafluoroisopropanol to form compounds comprising a natural product-like scaffold (quadrangularin) or its precursor depending on the aromatic substituents. The addition of a catalytic amount of scandium triflate [Sc(OTf)] to the reaction system altered the reaction outcome to give a different natural product-like compound, a pallidol-type dimer.
View Article and Find Full Text PDFInt J Mol Sci
April 2024
Quantum RedOx Chemistry Team, Institute for Quantum Life Science (iQLS), Quantum Life and Medical Science Directorate (QLMS), National Institutes for Quantum Science and Technology (QST), Chiba-shi 263-8555, Chiba, Japan.
2-Phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide (PTIO), a persistent nitronyl nitroxide radical, has been used for the detection and trapping of nitric oxide, as a redox mediator for batteries, for the activity estimation of antioxidants, and so on. However, there is no report on the reactivity of PTIO in the presence of redox-inactive metal ions. In this study, it is demonstrated that the addition of scandium triflate, Sc(OTf) (OTf = OSOCF), to an acetonitrile (MeCN) solution of PTIO resulted in an electron-transfer disproportionation to generate the corresponding cation (PTIO) and anion (PTIO), the latter of which is suggested to be stabilized by Sc to form [(PTIO)Sc].
View Article and Find Full Text PDFParasitol Res
February 2024
Institute of Specific Prophylaxis and Tropical Medicine, Center for Pathophysiology, Infectiology and Immunology, Medical University of Vienna, Vienna, Austria.
The parasite Entamoeba histolytica is the cause of amoebic dysentery and liver abscess in humans. On the protozoan cell surface, a variety of glycosylated molecules are involved in the interaction with the environment, such as attachment to the colonic mucus. One of these molecules is the lipopeptidophosphoglycan (LPPG), a complex surface component with antigenic properties.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
February 2024
Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, 116023, China.
The construction of multiple continuous fully substituted carbon centers, which serve as unique structural motif in natural products, is a challenging topic in organic synthesis. Herein, we report a hydrated [3+2] cyclotelomerization of butafulvenes to create contiguous fully substituted carbon backbone. In the presence of scandium triflate, all-carbon skeleton with spiro fused tricyclic ring can be constructed in high diastereoselectivity by utilizing butafulvene as the synthon.
View Article and Find Full Text PDFMolecules
June 2023
Department of Chemistry and Nano Science, Ewha Womans University, Seoul 03760, Republic of Korea.
A neutral, stable radical, 2,2-diphenyl-1-picrylhydrazyl radical (DPPH), has been frequently used to estimate the activity of antioxidants for more than 60 years. However, the number of reports about the effect of metal ions on the reactivity of DPPH is quite limited. We have recently reported a unique electron-transfer disproportionation of DPPH to produce the DPPH cations (DPPH) and anions (DPPH) upon the addition of scandium triflate [Sc(OTf) (OTf = OSOCF)] to an acetonitrile (MeCN) solution of DPPH.
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