1866-39-3Relevant academic research and scientific papers
Preparation of high-magnetization Fe3O4-NH 2-Pd (0) catalyst for heck reaction
Ma, Mingliang,Zhang, Qiuyu,Yin, Dezhong,Dou, Jinbo,Zhang, Hepeng,Xu, Hailong
, p. 168 - 172 (2012)
A magnetically separable Fe3O4-NH2-Pd (0) catalyst was easily synthesized by immobilizing Pd nanoparticles on the surface of magnetic Fe3O4-NH2 microspheres. It was found that the combination of Fe3O4 and triethylene tetramine (TETA) could give rise to structurally stable catalytic sites. Furthermore, the high-magnetization Fe3O4-NH 2-Pd(0) catalyst can be recovered by magnet and reused for six runs for Heck reaction without significant loss in catalytic activity.
One-pot synthesis of l-dopa-functionalized water-dispersible magnetite nano-palladium catalyst and its application in the Suzuki and Heck reactions in water: A novel and highly active catalyst
Niu, Jianrui,Wang, Fushan,Zhu, Xiaohang,Zhao, Jiahui,Ma, Jiantai
, p. 37761 - 37766 (2014)
A palladium catalyst supported on water-dispersible magnetite nanoparticles end-functionalized with amino and carboxyl groups was successfully prepared by a facile one-pot template-free method combined with a metal adsorption-reduction procedure. It was characterized by TEM, XRD, XPS, FT-IR and VSM. This catalyst exhibits excellent catalytic activity for Suzuki and Heck reactions in water. Furthermore, the newly developed catalyst is easy to be recovered and recycled by magnetic separation from aqueous phase reactions. More importantly, the catalyst revealed high efficiency and high stability under the reaction conditions and during recycling stages. This catalyst can be used consecutively six times without significant loss in catalytic activity. the Partner Organisations 2014.
Synthesis, characterization, luminescence, antibacterial, and catalytic activities of a palladium(II) complex involving a Schiff base
Ma, De-Yun,Zhang, Le-Xin,Rao, Xuan-Ye,Wu, Tong-Liang,Li, Dong-Hao,Xie, Xiao-Qun
, p. 1486 - 1496 (2013)
A new Pd(II) complex of fluorine-containing Schiff base ligand, [Pd 2(L)2Cl2] (1) [L = N-(4-fluorobenzylidene)-2,6- diethylbenzenamine], has been synthesized using solvothermal method and characterized by elemental analysis, IR-spectroscopy, thermogravimetric analysis, powder X-ray diffraction, UV-vis absorption spectra, and single-crystal X-ray diffraction Complex 1 is a μ-chloro-bridged dinuclear cyclometallated Pd(II) complex Thermal analysis indicates that 1 is quite stable to heat 1 exhibits quadruple emissions in the solid state (λ max = 766 nm) and possesses fluorescence lifetimes (τ1 = 87.20 ns, τ2 = 190.45 ns, and τ3 = 1805.10 ns at 616 nm); broad structureless bands at 690-800 nm are tentatively assigned to an excimeric 3IL transition The Schiff base (L) and its palladium(II) compound (1) have been screened for their antibacterial activity against several bacteria, and the results are compared with the activity of penicillin Moreover, 1 has been shown to be highly effective in the Heck reaction of 4-bromotoluene with acrylic acid
Pd-Catalyzed desulfitative arylation of olefins by: N -methoxysulfonamide
Ojha, Subhadra,Panda, Niranjan
supporting information, p. 1292 - 1298 (2022/02/19)
A novel Pd-catalyzed protocol for the desulfitative Heck-type reaction of N-methoxy aryl sulfonamides with alkenes was reported. The cross-coupling reaction was performed successfully with a variety of olefins to obtain aryl alkenes. Different substituents on the aromatic ring of N-methoxysulfonamides were also found to be compatible with the reaction conditions. Expectedly, the reaction proceeds through CuCl2-promoted generation of the nitrogen radical and subsequent desulfonylation under thermal conditions to afford the aryl radical for the Pd-catalyzed coupling reaction. N-Methoxysulfonamide was further exploited for the synthesis of symmetrical biaryls in the presence of CuCl2. This journal is
Photocatalytic Oxidative [2+2] Cycloelimination Reactions with Flavinium Salts: Mechanistic Study and Influence of the Catalyst Structure
Hartman, Tomá?,Reisnerová, Martina,Chudoba, Josef,Svobodová, Eva,Archipowa, Nataliya,Kutta, Roger Jan,Cibulka, Radek
, p. 373 - 386 (2021/02/01)
Flavinium salts are frequently used in organocatalysis but their application in photoredox catalysis has not been systematically investigated to date. We synthesized a series of 5-ethyl-1,3-dimethylalloxazinium salts with different substituents in the positions 7 and 8 and investigated their application in light-dependent oxidative cycloelimination of cyclobutanes. Detailed mechanistic investigations with a coumarin dimer as a model substrate reveal that the reaction preferentially occurs via the triplet-born radical pair after electron transfer from the substrate to the triplet state of an alloxazinium salt. The very photostable 7,8-dimethoxy derivative is a superior catalyst with a sufficiently high oxidation power (E=2.26 V) allowing the conversion of various cyclobutanes (with Eox up to 2.05 V) in high yields. Even compounds such as all-trans dimethyl 3,4-bis(4-methoxyphenyl)cyclobutane-1,2-dicarboxylate can be converted, whose opening requires a high activation energy due to a missing pre-activation caused by bulky adjacent substituents in cis-position.
Iron-catalyzed domino decarboxylation-oxidation of α,β-unsaturated carboxylic acids enabled aldehyde C-H methylation
Gong, Pei-Xue,Xu, Fangning,Cheng, Lu,Gong, Xu,Zhang, Jie,Gu, Wei-Jin,Han, Wei
supporting information, p. 5905 - 5908 (2021/06/18)
A practical and general iron-catalyzed domino decarboxylation-oxidation of α,β-unsaturated carboxylic acids enabling aldehyde C-H methylation for the synthesis of methyl ketones has been developed. This mild, operationally simple method uses ambient air as the sole oxidant and tolerates sensitive functional groups for the late-stage functionalization of complex natural-product-derived and polyfunctionalized molecules.
Amino Group Functionalized Hf-Based Metal-Organic Framework for Knoevenagel-Doebner Condensation
Das, Aniruddha,Anbu, Nagaraj,Gogoi, Chiranjib,Dhakshinamoorthy, Amarajothi,Biswas, Shyam
, p. 3396 - 3403 (2021/08/20)
A Hf(IV) metal-organic framework (MOF) with di-amino functionalized linker was obtained as a crystalline solid with UiO-67 topology under solvothermal reaction conditions. The guest free form of Hf(IV) MOF (1′) was efficiently employed as a heterogeneous catalyst to synthesize cinnamic acid derivatives via Knoevenagel-Doebner reaction for the first time. The catalyst (1′) was efficiently active to directly achieve cinnamic acid from benzaldehyde and malonic acid. The solid retained its activity up to 6th cycle with no decay in its activity. The noticeable advantages of the catalyst are its milder reaction conditions, high yield, high stability, recyclable nature towards catalysis and wide substrate scope as well as shape-selective behaviour. The possible mechanism of the reaction was also studied thoroughly with suitable control experiments.
Enantioselective Rauhut–Currier Reaction with β-Substituted Acrylamides Catalyzed by N-Heterocyclic Carbenes
Pitchumani, Venkatachalam,Breugst, Martin,Lupton, David W.
supporting information, p. 9413 - 9418 (2021/12/09)
β-Substituted acrylamides have low electrophilicity and are yet to be exploited in the enantioselective Rauhut–Currier reaction. By exploiting electron-withdrawing protection of the amide and moderate nucleophilicity N-heterocyclic carbenes, such substrates have been converted to enantioenriched quinolones. The reaction proceeds with complete diastereoselectivity, good yield, and modest enantioselectivity. Derivatizations are reported, as are computational studies, supporting decreased amide bond character with electron-withdrawing protection of the nitrogen.
Discovery of Novel Benzothiazepinones as Irreversible Covalent Glycogen Synthase Kinase 3β Inhibitors for the Treatment of Acute Promyelocytic Leukemia
Zhang, Peng,Min, Zhihui,Gao, Yang,Bian, Jiang,Lin, Xin,He, Jie,Ye, Deyong,Li, Yilin,Peng, Chao,Cheng, Yunfeng,Chu, Yong
, p. 7341 - 7358 (2021/06/28)
Recently, irreversible inhibitors have attracted great interest in antitumors due to their advantages of forming covalent bonds to target proteins. Herein, some benzothiazepinone compounds (BTZs) have been designed and synthesized as novel covalent GSK-3β inhibitors with high selectivity for the kinase panel. The irreversible covalent binding mode was identified by kinetics and mass spectrometry, and the main labeled residue was confirmed to be the unique Cys14 that exists only in GSK-3β. The candidate 4-3 (IC50 = 6.6 μM) showed good proliferation inhibition and apoptosis-inducing ability to leukemia cell lines, low cytotoxicity on normal cell lines, and no hERG inhibition, which hinted the potential efficacy and safety. Furthermore, 4-3 exhibited decent pharmacokinetic properties in vivo and remarkably inhibited tumor growth in the acute promyelocytic leukemia (APL) mouse model. All the results suggest that these newly irreversible BTZ compounds might be useful in the treatment of cancer such as APL.
Chlorination Reaction of Aromatic Compounds and Unsaturated Carbon-Carbon Bonds with Chlorine on Demand
Liu, Feng,Wu, Na,Cheng, Xu
supporting information, p. 3015 - 3020 (2021/05/05)
Chlorination with chlorine is straightforward, highly reactive, and versatile, but it has significant limitations. In this Letter, we introduce a protocol that could combine the efficiency of electrochemical transformation and the high reactivity of chlorine. By utilizing Cl3CCN as the chloride source, donating up to all three chloride atom, the reaction could generate and consume the chlorine in situ on demand to achieve the chlorination of aromatic compounds and electrodeficient alkenes.
