Results 81 to 90 of about 834,266 (345)
Photocatalytic activation of C–H bonds is versatile but challenging for undergoing oriented conversion processes. Herein, a spatially site-isolated heterojunction (ZS-Vs/ZIS) of ZnIn2S4 with strong Lewis acidity (ZIS) and ZnS with S-vacancy (ZS-Vs) is ...
Jie Li +6 more
doaj +1 more source
Calcium‐Catalyzed Arene C−H Bond Activation by Low‐Valent AlI
The low‐valent ß‐diketiminate complex (DIPPBDI)Al is stable in benzene but addition of catalytic quantities of [(DIPPBDI)CaH]2 at 20 °C led to (DIPPBDI)Al(Ph)H (DIPPBDI=CH[C(CH3)N‐DIPP]2, DIPP=2,6‐diisopropylphenyl).
Steffen Brand +4 more
semanticscholar +1 more source
Time after time – circadian clocks through the lens of oscillator theory
Oscillator theory bridges physics and circadian biology. Damped oscillators require external drivers, while limit cycles emerge from delayed feedback and nonlinearities. Coupling enables tissue‐level coherence, and entrainment aligns internal clocks with environmental cues.
Marta del Olmo +2 more
wiley +1 more source
C–H bond activation of benzene and thiophene by photochemically generated rhenocene cation
A cationic rhenocene-acetonitrile adduct [Cp2Re(NCMe)](BF4)(1) reacted with an excess of benzene, thiophene, 2-methylthiophene, and pyrrole under UV irradiation to afford the C–H bond activation products [Cp2Re(H)R]BF4 (R = phenyl, 2-thienyl, 2-(5 ...
Hiroshi Ogino +3 more
doaj +1 more source
Modification of Purine and Pyrimidine Nucleosides by Direct C-H Bond Activation
Transition metal-catalyzed modifications of the activated heterocyclic bases of nucleosides as well as DNA or RNA fragments employing traditional cross-coupling methods have been well-established in nucleic acid chemistry.
Yong Liang, Stanislaw F. Wnuk
doaj +1 more source
Regioselective Formation of α-Vinylpyrroles from the Ruthenium-Catalyzed Coupling Reaction of Pyrroles and Terminal Alkynes Involving C–H Bond Activation [PDF]
The cationic ruthenium catalyst Ru3(CO)12/NH4PF6 was found to be highly effective for the intermolecular coupling reaction of pyrroles and terminal alkynes to give gem-selective α-vinylpyrroles.
Gao, Ruili, Yi, Chae S.
core +2 more sources
Multiple ETS family transcription factors bind mutant p53 via distinct interaction regions
Mutant p53 gain‐of‐function is thought to be mediated by interaction with other transcription factors. We identify multiple ETS transcription factors that can bind mutant p53 and found that this interaction can be promoted by a PXXPP motif. ETS proteins that strongly bound mutant p53 were upregulated in ovarian cancer compared to ETS proteins that ...
Stephanie A. Metcalf +6 more
wiley +1 more source
C − H bond activation is a ubiquitous reaction that remains a major challenge in chemistry. Although semiconductor-based photocatalysis is promising, the C − H bond activation mechanism remains elusive.
Xuejiao Wu +7 more
doaj +1 more source
The reaction of [(Cp*Ir)2(μ-dmpm)(μ-H)][OTf] (2) [Cp* = η5-C5Me5, dmpm = bis(dimethylphosphino)methane] with 2,3-dihydrofuran gives [(Cp*IrH)2(μ-dmpm){μ-(2,3-dihydrofuranyl)}][OTf] (3) in an isolated yield of 70% via the C− ...
Yoshinori Takahashi +2 more
doaj +1 more source
Activation of a C−H Bond in Indene by [(COD)Rh(μ_2-OH)]_2 [PDF]
The air- and water-tolerant hydroxy-bridged rhodium dimer [(COD)Rh(μ_2-OH)]_2 cleanly activates the aliphatic C−H bond in indene to generate [(COD)Rh(η^3-indenyl)].
Bercaw, John E. +2 more
core +1 more source

