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Microwave-Assisted Synthesis of a MK2 Inhibitor by Suzuki-Miyaura Coupling for Study in Werner Syndrome Cells [PDF]

open access: yesPharmaceuticals, 2015
Microwave-assisted Suzuki-Miyaura cross-coupling reactions have been employed towards the synthesis of three different MAPKAPK2 (MK2) inhibitors to study accelerated aging in Werner syndrome (WS) cells, including the cross-coupling of a 2-chloroquinoline
Mark C. Bagley   +5 more
doaj   +9 more sources

DNA-Compatible Suzuki-Miyaura Cross-Coupling Reaction of Aryl Iodides With (Hetero)Aryl Boronic Acids for DNA-Encoded Libraries [PDF]

open access: yesFrontiers in Chemistry, 2022
An efficient method for the C-C bond formation via water soluble Na2PdCl4/sSPhos mediated Suzuki-Miyaura cross-coupling reaction of DNA-conjugated aryl iodide with (het)aryl boronic acids has been developed.
Vijay Kumar Siripuram   +3 more
doaj   +2 more sources

Revealing the electron driven mechanism in metal catalyzed Kumada cross coupling reaction [PDF]

open access: yesScientific Reports
The electron motion mechanism of the metal-catalyzed Kumada cross-coupling reaction, which synthesizes biphenyl from chlorobenzene and phenylmagnesium chloride (a Grignard reagent) using a palladium (Pd) complex with an auxiliary phosphine ligand, is ...
Noriyuki Takai   +4 more
doaj   +2 more sources

Novel nickel-immobilized-SiO2-TiO2 fine particles in the presence of cetyltrimethylammonium bromide as a catalyst for ultrasound-assisted-Kumada cross-coupling reaction [PDF]

open access: yesHeliyon
Kumada cross-coupling reaction is useful for producing biphenyls, where nickel and copper have been widely investigated as catalysts but mainly homogeneous ones.
Dewi Agustiningsih   +6 more
doaj   +2 more sources

Synthesis of N-acetyl diazocine derivatives via cross-coupling reaction [PDF]

open access: yesBeilstein Journal of Organic Chemistry
Diazocines are photoswitches derived from azobenzenes by bridging the two phenyl rings in ortho position with a CH2CH2 group forming an eight membered (diazocine) ring.
Thomas Brandt   +5 more
doaj   +2 more sources

Photoredox-Catalyzed Decarboxylative Cross-Coupling Reaction to Synthesis Unsymmetrical Diarylmethanes [PDF]

open access: yesMolecules
The photoredox-catalyzed decarboxylative cross-coupling reaction of aryl acetic acids and aryl nitriles has been achieved under an argon atmosphere in high yields.
Guozhe Guo   +3 more
doaj   +2 more sources

Biogenic palladium nanostructures for Suzuki-Miyaura and Sonogashira cross-coupling reaction under mild reaction conditions

open access: yesCurrent Research in Green and Sustainable Chemistry, 2022
Biogenic palladium nanostructures (NS) are synthesized by utilising pomegranate peels which are generally considered as agro-wastes. A simple methodology without the use of external reducing agent has been applied to achieve uniform flowerlike ...
Sameeran Kumar Das   +7 more
doaj   +1 more source

Cobalt-immobilized carbon-based nano-catalyst for CN cross coupling reaction

open access: yesResults in Chemistry, 2022
CN cross coupling reaction is very important in synthesis of pharmaceuticals, natural products, agrochemicals, fine chemicals and functional materials. Traditionally, palladium or copper metals are used for CN coupling reaction.
Shubham R. Bankar   +2 more
doaj   +1 more source

Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications

open access: yesMolecules, 2022
Hiyama cross-coupling is a versatile reaction in synthetic organic chemistry for the construction of carbon–carbon bonds. It involves the coupling of organosilicons with organic halides using transition metal catalysts in good yields and high ...
Rida Noor   +7 more
doaj   +1 more source

Cross-coupling Reactions of Monosubstituted Tetrazines [PDF]

open access: yesOrganic Letters, 2021
A fast and mild method for the Pd-catalyzed cross-coupling reaction of monosubstituted 3-bromo-1,2,4,5-tetrazine is presented. Investigation of silver-based additives revealed that Ag2CO3 is the optimal mediator, enabling the process without the need for strong bases or high temperatures.
Hoff, Lukas V   +4 more
openaire   +3 more sources

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