Results 201 to 210 of about 220,271 (263)
Chronobiology of Cancer: How Aging Fuels Oncogenesis at the Molecular Level
This graphical abstract illustrates the key biological pathways linking aging with cancer development and progression. In the upper left, cumulative exposure to ultraviolet radiation, toxins, and reactive oxygen species (ROS) causes DNA damage and genomic instability, whereas age‐related decline in repair mechanisms, such as ATM/ATR, BER, and NER ...
Anu Singh, Aroonima Misra, Sufian Zaheer
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ChemInform, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Fumitoshi Kakiuchi, Naoto Chatani
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AbstractFor Abstract see ChemInform Abstract in Full Text.
Fumitoshi Kakiuchi, Naoto Chatani
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Understanding and Exploiting C—H Bond Activation
ChemInform, 2002AbstractFor Abstract see ChemInform Abstract in Full Text.
Labinger, Jay A., Bercaw, John E.
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C–H bond activation of ethylene by a zirconacycle
Chemical Communications, 2013The reaction of C2H4 and β-SiH containing azasilazirconacycle Cp2Zr{κ(2)-N(SiHMe2)SiHMeCH2} (3), formed via a γ-abstraction reaction of Cp2Zr{N(SiHMe2)2}H (1), follows an unusual pathway in which a rare σ-bond metathesis reaction of ethylene generates a vinyl intermediate. That species undergoes a β-hydrogen abstraction under the reaction conditions to
KaKing, Yan, Aaron D, Sadow
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Metal-catalysed C–H bond activation and borylation
Chemical Society Reviews, 2022Transition metal-catalysed direct borylation of hydrocarbons via C–H bond activation has received a remarkable level of attention as a popular reaction in the synthesis of organoboron compounds owing to their synthetic versatility.
Ranjana Bisht +5 more
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Iron-Catalyzed C–H Bond Activation
Chemical Reviews, 2017Catalytic C-H bond activation, which was an elusive subject of chemical research until the 1990s, has now become a standard synthetic method for the formation of new C-C and C-heteroatom bonds. The synthetic potential of C-H activation was first described for ruthenium catalysis and is now widely exploited by the use of various precious metals.
Rui Shang +2 more
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The Chemistry of CH Bond Activation on Diamond
Chemistry – An Asian Journal, 2010AbstractThe surface of hydrogen‐terminated diamond resembles a solid hydrocarbon substrate. Interestingly, the CH bonds on the diamond surface are not as unreactive as that of saturated hydrocarbon molecules owing to its unique surface electronic properties.
Yu Lin, Zhong, Kian Ping, Loh
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Catalytic activation of aromatic CH bonds
Journal of Organometallic Chemistry, 1982Abstract A new reaction is described, involving oxidative addtion of aromatic bromides to palladium(O), two successive insertions of norbornene, and ring closure to the aromatic carbon ortho to the carbon originally bearing the bromine.
CATELLANI, Marta, CHIUSOLI, Gian Paolo
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Oxygen‐Promoted CH Bond Activation at Palladium
Angewandte Chemie International Edition, 2014Abstract[Pd(P(Ar)(tBu)2)2] (1, Ar=naphthyl) reacts with molecular oxygen to form PdII hydroxide dimers in which the naphthyl ring is cyclometalated and one equivalent of phosphine per palladium atom is released. This reaction involves the cleavage of both CH and OO bonds, two transformations central to catalytic aerobic oxidizations of hydrocarbons ...
Scheuermann, Margaret L. +7 more
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