Although cyclopropanation with donor/acceptor carbenes can be conducted under low catalyst loadings (<0.001 mol %), such low loading has not been generally effective for other classes of carbenes such as acceptor carbenes. In this current study, we demonstrate that ethyl diazoacetate can be effectively used in the cyclopropanation of -Boc-2,5-dihydropyrrole with dirhodium(II) catalyst loadings of 0.005 mol %. By appropriate choice of catalyst and hydrolysis conditions, either the - or -3-azabicyclo[3.1.0]hexanes can be formed cleanly with high levels of diastereoselectivity with no chromatographic purification.
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http://dx.doi.org/10.1021/acs.orglett.3c03652 | DOI Listing |
RSC Adv
January 2025
Department of Chemistry, Faculty of Science, Suez Canal University Ismailia 41522 Egypt +201113343594.
Achieving a net-zero emissions economy requires significant decarbonization of the transportation sector, which depends on the development of highly efficient electrocatalysts. Electrolytic water splitting is a promising approach to this end, with Ni-Mo alloys emerging as strong candidates for hydrogen production catalysts. This study investigates the electrodeposition of Ni and Ni-Mo nanostructured alloys with high molybdenum content onto low-carbon steel cathodes using a novel alkaline green lactate bath.
View Article and Find Full Text PDFRSC Adv
January 2025
Laboratory of Clean Low-Carbon Energy, Department of Thermal Science and Energy Engineering, University of Science and Technology of China Hefei 230023 PR China.
Crafting highly dispersed active metal sites on catalysts is an optimal method for improving the catalytic reactivity and stability, as it would improve atomic utilization efficiency, enhance reactant adsorption and activation ability through unique geometric and electronic properties. In this study, two synthesis methods were employed (ammonia evaporation (AE) and the impregnation method (IM)) to load Rh species onto the ZSM-5 support in order to attain tunable dispersivity, during which a 1.25-fold increase in the total yield of liquid oxygenated products (32 433.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
Department of Optoelectronic Information of Science and Engineering, School of Science, Jiangsu University of Science and Technology, Zhenjiang 212100, China.
Reasonable design of hydrogen evolution reaction (HER) electrocatalysts with low Pt loading and excellent catalytic performance is a key challenge in finding efficient and cost attractive catalysts. Pt with its unique d-electrons provides new opportunities for the development of HER catalysts when it forms compounds with highly earth-abundant C. Herein, we focused on designing highly efficient catalysts composed of Pt and C elements using first-principles structure search simulations, identifying four stability PtC monolayers.
View Article and Find Full Text PDFSmall Methods
January 2025
Department of Physics, Tamkang University, Tamsui, 25137, Taiwan.
This investigation explores the potential of co-incorporating nickel (Ni) and cobalt (Co) into copper oxide (CuO) nanostructures for bifunctional electrochemical charge storage and oxygen evolution reactions (OER). A facile wet chemical synthesis method is employed to co-incorporate Ni and Co into CuO, yielding diverse nanostructured morphologies, including rods, spheres, and flake. The X-ray diffraction (XRD) and Raman analyses confirmed the formation of NiCo-CuO nanostructure, with minor phases of nickel oxide (NiO) and cobalt tetraoxide (CoO).
View Article and Find Full Text PDFNat Commun
January 2025
Faculty of Physics, Astronomy and Applied Computer Science, Jagiellonian University, PL 30-348, Krakow, Poland.
Atomically precise synthesis of graphene nanostructures on semiconductors and insulators has been a formidable challenge. In particular, the metallic substrates needed to catalyze cyclodehydrogenative planarization reactions limit subsequent applications that exploit the electronic and/or magnetic structure of graphene derivatives. Here, we introduce a protocol in which an on-surface reaction is initiated and carried out regardless of the substrate type.
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