Results 11 to 20 of about 7,841,789 (286)
When transition-metal-catalyzed C–H activation meets allene chemistry
Transition-metal-catalyzed allenes-involved C–H functionalizations demonstrate unique selectivity and undergo exceptional pathways due to the existence of elusive orthogonal cumulative CCC bonds.
Shu-Meng Deng +2 more
doaj +1 more source
Functionalization of Porphyrins Using Metal-Catalyzed C–H Activation
The review is devoted to the C–H functionalization of porphyrins. Porphyrins exhibit the properties of organic semiconductors, light energy converters, chemical and electrochemical catalysts, and photocatalysts.
Aleksey N. Kiselev +3 more
doaj +1 more source
Rollover cyclometalation constitutes a particular case of cyclometallation reaction. This reaction occurs when a chelated heterocyclic ligand loses its bidentate coordination mode and undergoes an internal rotation, after which a remote C–H bond is ...
Antonio Zucca, Maria I. Pilo
doaj +1 more source
A synthetic, catalytic and theoretical investigation of an unsymmetrical SCN pincer palladacycle [PDF]
The SCN ligand 2-{3-[(methylsulfanyl)methyl]phenyl}pyridine, 1, has been synthesized starting from an initial Suzuki–Miyaura (SM) coupling between 3-((hydroxymethyl)phenyl)boronic acid and 2-bromopyridine.
Gavin W. Roffe +10 more
doaj +1 more source
Coumarins Synthesis and Transformation via C–H Bond Activation—A Review
For several decades, coumarins have attracted considerable attention due to the fact of their application in diverse fields such as medical science and biomedical research as well as several industrial branches.
Katarzyna Szwaczko
doaj +1 more source
Bonds between hydrogen and carbon atoms are the most frequent type of bonds in organic molecules. The ability to replace hydrogen atoms by making other types of bonds to carbon atoms can enable simpler access to complex organic molecules by substituting
Jyoti Dhankhar, Ilija Čorić
doaj +1 more source
Ligand Lone-Pair Influence on Hydrocarbon C-H Activation: A Computational Perspective [PDF]
Mid to late transition metal complexes that break hydrocarbon C-H bonds by transferring the hydrogen to a heteroatom ligand while forming a metal-alkyl bond offer a promising strategy for C-H activation.
Cundari, Thomas R. +4 more
core +2 more sources
A catalytic cycle for oxidation of tert-butyl methyl ether by a double C−H activation-group transfer process [PDF]
A square-planar, iridium(I) carbene complex is shown to effect atom and group transfer from nitrous oxide and organic azides, releasing the corresponding formate or formimidate and an iridium(I)−dinitrogen adduct.
Grubbs, Robert H., Whited, Matthew T.
core +2 more sources
The continuum of carbon–hydrogen (C–H) activation mechanisms and terminology
As a rapidly growing field across all areas of chemistry, C-H activation/functionalisation is being used to access a wide range of important molecular targets.
Kristof M. Altus, J. Love
semanticscholar +1 more source
Intra- and Intermolecular C−H Activation by Bis(phenolate)pyridineiridium(III) Complexes [PDF]
A bis(phenolate)pyridine pincer ligand (henceforth abbreviated as ONO) has been employed to support a variety of iridium complexes in oxidation states I, III, and IV.
Bercaw, John E. +2 more
core +2 more sources

