Results 31 to 40 of about 2,467,830 (354)
Manganese-Catalyzed C–H Activation
Manganese is found in the active center of numerous enzymes that operate by an outer-sphere homolytic C–H cleavage. Thus, a plethora of bioinspired radical-based C–H functionalizations by manganese catalysis have been devised during the past decades. In contrast, organometallic C–H activation by means of manganese catalysis has emerged only recently as
Weiping Liu, Lutz Ackermann
openaire +2 more sources
Lowering the C-H Bond Activation Barrier of Methane Using SAC@Cu(111): A Periodic DFT Investigations
Methane has long captured the world\u27s spotlight for being the simplest and yet one of the most notorious hydrocarbon. Exploring its potential to be converted into value added products has raised a compelling interest.
Meema, Bhati +2 more
core +1 more source
Photoinduced homolytic C–H activation in N-(4-homoadamantyl)phthalimide
N-(4-homoadamantyl)phthalimide (5) on excitation and population of the triplet excited state underwent intramolecular H-abstractions and gave products 6 and 7.
Nikola Cindro +4 more
doaj +1 more source
Enantioselective Rhodium-Catalyzed C–C Bond Activations
The catalytic activation of carbon–carbon single bonds represents a major challenge in organometallic chemistry. Strained ring substrates occupy in this respect a privileged role as their inherent ring strain facilitates the desired metal ...
Tobias Seiser, Nicolai Cramer
doaj +1 more source
Rh(III)-catalyzed directed C–H bond amidation of ferrocenes with isocyanates
[RhCp*(OAc)2(H2O)] [Cp* = pentamethylcyclopentadienyl] catalyzed the C–H bond amidation of ferrocenes possessing directing groups with isocyanates in the presence of 2 equiv/Rh of HBF4·OEt2.
Satoshi Takebayashi +3 more
doaj +1 more source
C-H Bond Activation via Concerted Metalation-Deprotonation at a Palladium(III) Center
Herein we report the direct observation of C-H bond activation at an isolated mononuclear Pd(III) center. The oxidation of the Pd(II) complex (MeN4)PdII(neophyl)Cl (neophyl = -CH2C(CH3)2Ph; MeN4 = N,N′-di-tert-butyl-2,11-diaza[3.3](2,6)pyridinophane ...
Dae Young, Bae +3 more
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Palladium-catalyzed late-stage diversification of structurally complex peptides has major shortcomings. Here, the authors developed a ruthenium-catalyzed C–H alkylations of peptides allowing for fluorescence labeling, late-stage diversifications and ...
Alexandra Schischko +5 more
doaj +1 more source
On the Use of Iron in Organic Chemistry
Transition metal catalysis in modern organic synthesis has largely focused on noble transition metals like palladium, platinum and ruthenium. The toxicity and low abundance of these metals, however, has led to a rising focus on the development of the ...
Arnar Guðmundsson, Jan-E. Bäckvall
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Modular construction of multiple functionalized arenes from abundant feedstocks, stands as an unremitting pursue goal in synthetic chemistry, which would accelerate the discovery of new drugs an advanced materials.
Jianhang, Rao +6 more
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A mild and facile Cp*Rh(III)-catalyzed C–H activation and intramolecular cascade annulation protocol has been proposed for the furnishing of highly fused isochromeno-1,2-benzothiazines scaffolds using S-phenylsulfoximides and 4-diazoisochroman-3-imine as
Bao Wang +4 more
doaj +1 more source

