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71.
In this paper all efforts have been devoted to develop stabilized tannic acid-SO3H on Fe3O4@SiO2 nanoparticles as the new magnetically and eco-friendly nanocatalyst. This nanocatalyst was identified using different techniques such as fourier transform infrared (FT-IR), Powder X-ray diffraction (XRD), vibrating sample magnetometry (VSM), scanning electron microscopy (SEM), energy dispersive x-ray spectroscopy (EDXS) and thermogravimetric analysis (TGA). Catalytic performance of the catalyst in cyclocondensation reaction of anthranilamide with different aldehydes under the friendly environmentally reaction condition led to formation corresponding 2,3-dihydro-4(1H)-quinazolinones compounds in excellent yields. The catalyst could be easily recovered by an external magnet and reused 4 times without significant loss of catalytic activity. 相似文献
72.
《Electrochemistry communications》2007,9(3):354-360
In this paper, we prepared TiO2@CdS core–shell nanorods films electrodes using a simple and low-cost chemical bath deposition method. The core–shell nanorods films electrodes were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and UV–vis spectrometry techniques. After applying these TiO2@CdS core–shell nanorods electrodes in photovoltaic cells, we found that the photocurrent was dramatically enhanced, comparing with those of bare TiO2 nanorods and CdS films electrodes. Moreover, TiO2@CdS core–shell nanorods film electrode showed better cell performance than CdS nanoparticles deposited TiO2 nanoparticles (P25) film electrode. A photocurrent of 1.31 mA/cm2, a fill factor of 0.43, an open circuit photovoltage of 0.44 V, and a conversion efficiency of 0.8% were obtained under an illumination of 32 mW/cm2, when the CdS nanoparticles deposited on TiO2 nanorods film for about 20 min. The maximum quantum efficiency of 5.0% was obtained at an incident wavelength of 500 nm. We believe that TiO2@CdS core–shell heterostructured nanorods are excellent candidates for studying some fundamental aspects on charge separation and transfer in the fields of photovoltaic cells and photocatalysis. 相似文献
73.
Frontispiece: Dirigent Proteins from Cotton (Gossypium sp.) for the Atropselective Synthesis of Gossypol 下载免费PDF全文
74.
Metal‐Free,Room‐Temperature,Radical Alkoxycarbonylation of Aryldiazonium Salts through Visible‐Light Photoredox Catalysis 下载免费PDF全文
Wei Guo Dr. Liang‐Qiu Lu Yue Wang Ya‐Ni Wang Jia‐Rong Chen Prof. Dr. Wen‐Jing Xiao 《Angewandte Chemie (International ed. in English)》2015,54(7):2265-2269
The first radical alkoxycarboxylation of aryldiazonium salts using CO gas through visible‐light‐induced photoredox catalysis (16 W blue LEDs) has been developed. This reaction is entirely metal‐free, is carried out at room temperature with a low loading of an organic dye as a photocatalyst (0.5 mol %), and provides a wide range of arylcarboxylic acid esters in high yields. Importantly, this photocatalytic system can be successfully extended to other carboxylation reactions. 相似文献
75.
Enantioselective Palladium‐Catalyzed Insertion of α‐Aryl‐α‐diazoacetates into the OH Bonds of Phenols 下载免费PDF全文
Xiu‐Lan Xie Prof. Shou‐Fei Zhu Jun‐Xia Guo Yan Cai Prof. Qi‐Lin Zhou 《Angewandte Chemie (International ed. in English)》2014,53(11):2978-2981
A palladium‐catalyzed asymmetric O? H insertion reaction was developed. Palladium complexes with chiral spiro bisoxazoline ligands promoted the insertion of α‐aryl‐α‐diazoacetates into the O? H bond of phenols with high yield and excellent enantioselectivity under mild reaction conditions. This palladium‐catalyzed asymmetric O? H insertion reaction provided an efficient and highly enantioselective method for the preparation of synthetically useful optically active α‐aryl‐α‐aryloxyacetates. 相似文献
76.
Rhodium(III)‐Catalyzed Alkenylation Reactions of 8‐Methylquinolines with Alkynes by C(sp3)H Activation 下载免费PDF全文
Bingxian Liu Tao Zhou Prof. Dr. Bin Li Prof. Shansheng Xu Prof. Dr. Haibin Song Prof. Dr. Baiquan Wang 《Angewandte Chemie (International ed. in English)》2014,53(16):4191-4195
The alkenylation reactions of 8‐methylquinolines with alkynes, catalyzed by [{Cp*RhCl2}2], proceeds efficiently to give 8‐allylquinolines in good yields by C(sp3)? H bond activation. These reactions are highly regio‐ and stereoselective. A catalytically competent five‐membered rhodacycle has been structurally characterized, thus revealing a key intermediate in the catalytic cycle. 相似文献
77.
Enantioselective NH Insertion Reaction of α‐Aryl α‐Diazoketones: An Efficient Route to Chiral α‐Aminoketones 下载免费PDF全文
Bin Xu Prof. Shou‐Fei Zhu Xiao‐Dong Zuo Zhi‐Chao Zhang Prof. Qi‐Lin Zhou 《Angewandte Chemie (International ed. in English)》2014,53(15):3913-3916
A highly enantioselective N? H insertion reaction of α‐diazoketones was developed by using cooperative catalysis by dirhodium(II) carboxylates and chiral spiro phosphoric acids. The insertion reaction provides a new access route to diverse chiral α‐aminoketones, which are versatile building blocks in organic synthesis, with fast reaction rates, good yields and high enantioselectivity under mild and neutral conditions. 相似文献
78.
Merging Aerobic Oxidation and Enamine Catalysis in the Asymmetric α‐Amination of β‐Ketocarbonyls Using N‐Hydroxycarbamates as Nitrogen Sources 下载免费PDF全文
Changming Xu Dr. Long Zhang Prof. Dr. Sanzhong Luo 《Angewandte Chemie (International ed. in English)》2014,53(16):4149-4153
We describe herein an unprecedented asymmetric α‐amination of β‐ketocarbonyls under aerobic conditions. The process is enabled by a simple chiral primary amine through the coupling of a catalytic enamine ester intermediate and a nitrosocarbonyl (generated in situ) derived from N‐hydroxycarbamate. The reaction features high chemoselectivity and excellent enantioselectivity for a broad range of substrates. 相似文献
79.
Maintenance of Amyloid β Peptide Homeostasis by Artificial Chaperones Based on Mixed‐Shell Polymeric Micelles 下载免费PDF全文
Fan Huang Jianzu Wang Aoting Qu Liangliang Shen Dr. Jinjian Liu Jianfeng Liu Dr. Zhenkun Zhang Yingli An Prof. Linqi Shi 《Angewandte Chemie (International ed. in English)》2014,53(34):8985-8990
The disruption of Aβ homeostasis, which results in the accumulation of neurotoxic amyloids, is the fundamental cause of Alzheimer’s disease (AD). Molecular chaperones play a critical role in controlling undesired protein misfolding and maintaining intricate proteostasis in vivo. Inspired by a natural molecular chaperone, an artificial chaperone consisting of mixed‐shell polymeric micelles (MSPMs) has been devised with tunable surface properties, serving as a suppressor of AD. Taking advantage of biocompatibility, selectivity toward aberrant proteins, and long blood circulation, these MSPM‐based chaperones can maintain Aβ homeostasis by a combination of inhibiting Aβ fibrillation and facilitating Aβ aggregate clearance and simultaneously reducing Aβ‐mediated neurotoxicity. The balance of hydrophilic/hydrophobic moieties on the surface of MSPMs is important for their enhanced therapeutic effect. 相似文献
80.
Intramolecular Metal‐Free Oxidative Aryl–Aryl Coupling: An Unusual Hypervalent‐Iodine‐Mediated Rearrangement of 2‐Substituted N‐Phenylbenzamides 下载免费PDF全文
Siyun Shang Dr. Daisy Zhang‐Negrerie Prof. Dr. Yunfei Du Prof. Dr. Kang Zhao 《Angewandte Chemie (International ed. in English)》2014,53(24):6216-6219
Hypervalent‐iodine‐mediated oxidative coupling of the two aryl groups in either 2‐acylamino‐N‐phenyl‐benzamides or 2‐hydroxy‐N‐phenylbenzamides, with concomitant insertion of the ortho‐substituted N or O atom into the tether, has been described for the first time. This unusual metal‐free rearrangement reaction involves an oxidative C(sp2)? C(sp2) aryl–aryl bond formation, cleavage of a C(sp2)? C(O) bond, and a lactamization/lactonization. Furthermore, unsymmetrical diaryl compounds can be easily obtained by removing the tether within the cyclized product. 相似文献