417548

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Immobilized palladium on surface-modified Fe3O4/SiO2 nanoparticles: as a magnetically separable and stable recyclable high-performance catalyst for Suzuki and Heck cross-coupling reactions

Du, Q.; et al.

Tetrahedron, 68, 3577-3584 (2012)

Nucleation, reorganization and disassembly of an active network from lactose-modified chitosan mimicking biological matrices.

Franco Furlani et al.

Carbohydrate polymers, 208, 451-456 (2019-01-20)

Developing synthetic materials able to mimic micro- and macrorheological properties of natural networks opens up to novel applications and concepts in materials science. The present contribution describes an active network based on a semi-synthetic polymer, a lactitol-bearing chitosan derivative (Chitlac)

Strategy used to synthesize high activity and low Pd catalyst for Suzuki coupling reaction: an experimental and theoretical investigation.

Xiao Yan et al.

Physical chemistry chemical physics : PCCP, 22(11), 6222-6230 (2020-03-05)

Unveiling the reaction mechanism is significant for developing high-performance catalysts. In this paper, a series of precisely controlled PdxM147-x (M = Cu, Pt, Au, Rh, Ru) dendrimer encapsulated nanoparticles (DENs) has been successfully synthesized. The mechanisms of PdxM147-x as catalysts

Copper-Mediated Aerobic Fluoroalkylation of Arylboronic Acids with Fluoroalkyl Iodides at Room Temperature

Qi, Q.; Shen, Q.; Lu, L.

Journal of the American Chemical Society, 134, 648-6551 (2012)

Pd-catalyzed direct arylation of phenylpyrazole: Synthesis of fipronil derivatives with aryl boronic acids promoted by a stoichiometric amount of NIS

Zhang, X-H.; Han, J-S.; Zhong, P.

Journal of Fluorine Chemistry, 137, 44-49 (2012)

Suzuki-Miyaura cross-coupling reaction of aryl bromides catalyzed by palladium(II) pyridoxal hydrazone complexes

Pandiarajan, D.; Ramesh, R.

Journal of Organometallic Chemistry, 708-709, 18-24 (2012)

A Double Suzuki Approach for Synthesis of Substituted Diarylmethylidenefluorenes

C. V. Ramana, et al.

Synlett, 1, 127-128 (2007)

Regioselective Arylation and Alkynylation of 2,3-Dibromo-1H-inden-1-one by Suzuki-Miyaura and Sonogashira Cross-Coupling Reactions

Khera, R. A.; et al.

Helvetica Chimica Acta, 95, 469-482 (2012)

Tandem-type Pd(II)-catalyzed oxidative Heck reaction/intramolecular C-H amidation sequence: a novel route to 4-aryl-2-quinolinones.

Kiyofumi Inamoto et al.

Chemical communications (Cambridge, England), 48(36), 4332-4334 (2012-03-24)

A novel catalytic method for synthesizing 4-aryl-2-quinolinones is reported. The process involves two mechanistically independent, sequential Pd(II)-catalyzed reactions--the oxidative Heck reaction and the intramolecular C-H amidation--both of which smoothly proceed in the presence of a single catalytic system in a

Cationic Pd(II)-catalyzed highly enantioselective arylative cyclization of alkyne-tethered enals or enones initiated by carbopalladation of alkynes with arylboronic acids.

Kun Shen et al.

Organic letters, 14(7), 1756-1759 (2012-03-28)

Cationic Pd(II)-catalyzed enantioselective arylative cyclization of alkyne-tethered enals or enones initiated by carbopalladation of alkynes was developed without the necessity of a redox system.

Short synthesis of 4-aryl-3-pyrrolin-2-ones

Sarah J.P.Yoon-Miller, et al.

Tetrahedron Letters, 48, 827-830 (2007)

Palladium(II) thiocarboxamide complexes: synthesis, characterisation and application to catalytic Suzuki coupling reactions.

Elangovan Sindhuja et al.

Dalton transactions (Cambridge, England : 2003), 41(17), 5351-5361 (2012-03-09)

A simple route to synthesise palladium(II) complexes from the reaction of N-substituted pyridine-2-thiocarboxamide ligands and PdCl(2)(PPh(3))(2) has been developed. The new complexes are very soluble in common solvents and have been fully characterised (elemental analysis, FT-IR, (1)H, (31)P, (13)C-NMR), including

Ligand-free copper-catalyzed coupling of nitroarenes with arylboronic acids

Zhang J, et al.

Green Chemistry, 14, 912-916 (2012)

Ruthenium(0)-catalyzed sp3 C-H bond arylation of benzylic amines using arylboronates.

Navid Dastbaravardeh et al.

Organic letters, 14(7), 1930-1933 (2012-03-28)

A Ru-catalyzed direct arylation of benzylic sp(3) carbons of acyclic amines with arylboronates is reported. This highly regioselective and efficient transformation can be performed with various combinations of N-(2-pyridyl) substituted benzylamines and arylboronates. Substitution of the pyridine directing group in

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