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A simple and highly efficient protocol has been developed for the Pd/C-catalyzed ligand-free Suzuki–Miyaura reaction of potassium aryltrifluoroborates. In this catalytic system, the results demonstrate that oxygen plays a positive role in the cross-coupling reaction. In addition, this catalytic system could be successfully applied to synthesize biaryl compounds containing a carbazole moiety and the catalyst was recycled seven times without significant loss of catalytic activity. 相似文献
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Yuxuan Liu Wang Miao Prof. Weijun Tang Prof. Dong Xue Prof. Jianliang Xiao Prof. Chao Wang Prof. Changzhi Li 《化学:亚洲杂志》2021,16(13):1725-1729
A rhodium terpyridine complex catalyzed transfer hydrogenation of nitroarenes to anilines with i-PrOH as hydrogen source and water as solvent has been developed. The catalytic system can work at a substrate/catalyst (S/C) ratio of 2000, with a turnover frequency (TOF) up to 3360 h−1, which represents one of the most active catalytic transfer hydrogenation systems for nitroarene reduction. The catalytic system is operationally simple and the protocol could be scaled up to 20 gram scale. The water-soluble catalyst bearing a carboxyl group could be recycled 15 times without significant loss of activity. 相似文献
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A highly efficient catalytic system without transition metals in water has been developed for aerobic oxidations of benzylic alcohols. The newly developed catalyst system could oxidize benzylic alcohols and heteroaromatic analogues with 1 mol % TEMPO as a catalyst and with a catalytic amount of 1,3-dibromo-5,5-dimethylhydantoin and NaNO2 as cocatalysts. Under the optimal conditions, various alcohols could be converted into their corresponding aldehydes or ketones in high yields. 相似文献
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From CO oxidation to CO2 activation: an unexpected catalytic activity of polymer-supported nanogold 总被引:5,自引:0,他引:5
A simple, clean, safe, and reproducible catalyst system, polymer-supported nanogold, was successfully developed for the fixation of CO2 to cyclic carbonate and for the carbonylation of amines to disubstituted ureas with unprecedented catalytic activity (TOF > 50 000 mol/mol/h and TOFP approximately 3000 mol/mol/h, respectively). To the best of our knowledge, it was the first to report that nanogold catalysts have exclusive catalytic activity for activation of carbon dioxide, and that the catalytic activity of the polymer-immobilized nanogold catalysts could be controlled by the particle size of the nanogold. 相似文献
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Zhenzhen Xia Lizhen Qin Weiyou Zhou Hui Wang Binxun Yu Zhonghua Sun Junfeng Qian Mingyang He 《Tetrahedron letters》2019,60(42):151121
An efficient and convenient heterogeneous catalytic procedure has been developed for the phosphonation of a-amino CH bonds with various dialkyl phosphites and diarylphosphine oxides using molecular oxygen as a sustainable oxidant over CoNiFe hydrotalcite. The catalytic system could tolerate various tetrahydroquinoline derivatives, and the corresponding a-amino phosphonic compounds could be obtained in good to excellent yields. Synergistic effect might exist in the oxidative phosphonation under the catalysis of CoNiFe hydrotalcite. 相似文献
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Azomethine ylides are useful intermediates for the rapid construction of chiral N‐containing compounds. However, its synthetic potential has not been fully developed due to the limited reaction models. In combination with synergistic catalysis and azomethine ylide chemistry, we have developed several types of novel catalytic system including Cu/Pd, Cu/Ir and PTC/Ir catalysis, which can convert readily‐available azomethine ylides to various high‐valued molecules such as unnatural α‐amino acids, homoallylic amines and N‐heterocycles. Compared with the traditional mono‐catalysis, the synergistic catalyst system exhibits enhanced catalytic efficiency and chiral induction ability in many cases. In addition, we have demonstrated that these strategies could be applied in the construction of bioactive compounds and natural products. 相似文献
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《Tetrahedron: Asymmetry》2004,15(4):743-746
A recyclable catalytic system for the asymmetric dihydroxylation of olefins was developed by using a mono-quaternized bis-cinchona alkaloid ligand 3 and OsO4 combined with PEG or an ionic liquid. Both the catalytic components could be recovered and reused in five consecutive reactions without any additional OsO4 or ligand. The catalytic system is effective in the AD reactions of seven olefins. 相似文献
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Jooyoung Chung Jinju Kim Youngjin Jang Sangmoon Byun Taeghwan Hyeon B. Moon Kim 《Tetrahedron letters》2013
We have developed a convenient Pd–Fe3O4 heterodimeric nanocrystal catalyst system for Heck and Sonogashira reactions. This catalyst offers an environment-friendly, atom-efficient, and robust catalytic system for both reactions. Furthermore the nanocrystal catalyst could be easily separated by an external magnet and recycled six times without losing its catalytic activity. 相似文献
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Recyclable and reusable Pd(OAc)2/DABCO/PEG-400 system for Suzuki-Miyaura cross-coupling reaction 总被引:2,自引:0,他引:2
[reaction: see text] A stable and efficient Pd(OAc)2/DABCO (triethylenediamine) catalytic system for Suzuki-Miyaura cross-coupling reaction has been developed. In the presence of Pd(OAc)2 and DABCO, coupling of aryl halides with arylboronic acids was carried out smoothly to afford good to excellent yields and high turnover numbers (TONs) (the maximal TONs were up to 960,000 for the reaction of 1-iodo-4-nitrobenzene with phenylboronic acid) using PEG-400 as the solvent. Moreover, the Pd(OAc)2/DABCO/PEG-400 system could be recycled and reused five times without any loss of catalytic activity for aryl iodides and bromides. 相似文献
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《Tetrahedron letters》2019,60(30):2005-2008
A new strategy for the synthesis of 2-Methylbenzofurans via the intramolecular Heck reaction has been developed. This efficient palladium-catalyzed system showed good catalytic activity. Various substituted 2-methylbenzofurans could be afforded in good to excellent yields. 相似文献
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Weiyou Zhou Dongwei Chen Fuan Sun Junfeng Qian Mingyang He Qun Chen 《Tetrahedron letters》2018,59(10):949-953
An efficient catalytic procedure has been developed for the aerobic oxidative dehydrogenation of N-heterocycles by cobalt porphyrin in the absence of any additives. The catalytic system could tolerate various 1,2,3,4-tetrahydroquinoline derivatives and some other N-heterocycles. The corresponding N-heteroaromatics could be obtained in 59–86% yields. The mechanism investigation suggested that the aerobic oxidative dehydrogenation might proceed with imine intermediate through radical paths. 相似文献
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A new and simple PdCl2/DMA catalytic system for the alcohol oxidation has been developed using molecular oxygen as the sole oxidant under mild conditions. The catalytic system could be reused for three runs without significant loss of catalytic activity. A variety of active and non-active alcohols were oxidized to their corresponding carbonyl compounds in good to excellent yields. Gas-uptake kinetics for the catalytic system was also investigated. The ca. 1:1 molar ratio of O2 uptake to product yield is observed, suggesting the in situ formation of H2O2. 相似文献
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Through tuning the surface wettability of interfacially active TiO2 particles, a pH-responsive Pickering emulsion system is formed, as in situ separation and recycling of the nano-catalysts system. 相似文献
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《化学:亚洲杂志》2017,12(18):2364-2368
A series of robust N‐heterocyclic carbene palladacycles have been successfully developed. These showed high catalytic activity and selectivity toward the challenging amination of N‐heteroaryl chlorides. Different primary and secondary amines were fully compatible with this catalytic system. Remarkably, no double amination products could be detected when primary amines were utilized in our catalytic transformation. Furthermore, the protocol has been successfully extended to synthesize rosiglitazone, a clinical drug for diabetes mellitus, highlighting its potential pharmaceutical feasibility. 相似文献
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Imidazolium-based polymer supported gadolinium triflate as a heterogeneous recyclable Lewis acid catalyst for Michael additions 总被引:1,自引:0,他引:1
A heterogeneous Lewis acid catalytic system has been developed by incorporating gadolinium triflate on to poly[styrene-co-(1-((4-vinylphenyl)methyl)-3-methylimidazolium) tetrafluoroborate] (1-Gd(OTf)3), and the catalytic activity of this system has been examined for Michael additions of amines and thiols to α,β-unsaturated esters and acrylonitrile. The reactions proceed in moderate to excellent yields in the presence of catalytic system 1-Gd(OTf)3. The catalytic system could be efficiently recycled and reused. 相似文献
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Selective aerobic oxidation of activated alcohols into acids or aldehydes in ionic liquids 总被引:1,自引:0,他引:1
Selective aerobic oxidation of activated primary alcohols into acids or aldehydes has been developed in ionic liquids. Under optimal conditions, various alcohols could be selectively converted into their corresponding acids or aldehydes in good to excellent yields. The newly developed catalytic systems could also be recycled and reused for three runs without any significant loss of catalytic activity. 相似文献
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A nonmetal catalytic system consisting of N-hydroxyphthalimide, xanthone, and tetramethylammonium chloride was developed. A wide range of hydrocarbons could be oxidized efficiently with dioxygen under mild conditions. In the presence of xanthone and tetramethylammonium chloride, catalytic activity of N-hydroxyphthalimide was greatly improved, and selectivity for alkyl hydroperoxide was remarkably decreased. 相似文献
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Xinye Yang Hui Xing Ye Zhang Yisheng Lai Yihua Zhang Yongwen Jiang Dawei Ma 《中国化学》2012,30(4):875-880
An efficient catalytic system of CuI/8‐hydroxyquinalidine was developed for the coupling of aryl iodides and indole as well as some azoles. The reaction could be carried out at 90°C under the condition of relatively low catalyst loading, affording various N‐arylindoles and N‐aryl azoles in good yields. The functionalized and hindered aryl iodides were suitable substrates for this transformation. 相似文献