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961.
Simple, economical, and environmentally friendly method to synthesize 2-alkylbenzimidazoles was developed by modifying the conventional method between o-phenylenediamine and aldehyde.  相似文献   
962.
963.
Structural information about the target–compound complex is invaluable in the early stage of drug discovery. In particular, it is important to know into which part of the initial compound additional interaction sites could be introduced to improve its affinity. Herein, we demonstrate that the affinity of a small‐molecule inhibitor for its target protein could be successfully improved by the constructive introduction of the interaction mode of a competitive peptide. The strategy involved the discrimination of overlapping and non‐overlapping peptide–compound pharmacophores by the use of a ligand‐based NMR spectroscopic approach, INPHARMA. The obtained results enabled the design of a new compound with improved affinity for the platelet receptor glycoprotein VI (GPVI). The approach proposed herein efficiently combines the advantages of compounds and peptides for the development of higher‐affinity druglike ligands.  相似文献   
964.
The photothermal conversion of CO2 provides a straightforward and effective method for the highly efficient production of solar fuels with high solar‐light utilization efficiency. This is due to several crucial features of the Group VIII nanocatalysts, including effective energy utilization over the whole range of the solar spectrum, excellent photothermal performance, and unique activation abilities. Photothermal CO2 reaction rates (mol h?1 g?1) that are several orders of magnitude larger than those obtained with photocatalytic methods (μmol h?1 g?1) were thus achieved. It is proposed that the overall water‐based CO2 conversion process can be achieved by combining light‐driven H2 production from water and photothermal CO2 conversion with H2. More generally, this work suggests that traditional catalysts that are characterized by intense photoabsorption will find new applications in photo‐induced green‐chemistry processes.  相似文献   
965.
The reaction of three types of carbon nanofibers (CNFs; platelet: CNF‐P, tubular: CNF‐T, herringbone: CNF‐H) with Ir4(CO)12 in mesitylene at 165 °C provided the corresponding CNF‐supported iridium nanoparticles, Ir/CNFs (Ir content=2.3–2.6 wt. %). Transmission electron microscopy (TEM) studies of these Ir/CNF samples revealed that size‐controlled Ir nanoparticles (average particle size of 1.1–1.5 nm) existed on the CNFs. Among the three Ir/CNF samples, Ir/CNF‐T showed an excellent catalytic activity and chemoselectivity towards hydrogenation of functionalized nitroarenes and imines; the corresponding aniline derivatives were obtained with high turnover numbers at ambient temperature under 10 atm of H2, and the catalyst is reusable. Ir/CNF‐T was also effective for the reductive N‐alkylation of anilines with carbonyl compounds.  相似文献   
966.
Aromatic ketones such as 4′‐methoxyacetophenone (MAP), acetophenone (AP), 4‐acetylbiphenyl (ABP), and 2‐acetyl‐6‐methoxynapthalene (AMN) interacted with fluoroalkyl end‐capped 2‐acrylamido‐2‐methylpropanesulfonic acid oligomer [RF‐(AMPS)n‐RF] at 80°C for 3 h to give the corresponding fluorinated oligomer/aromatic ketones composites. In these composites, the RF‐(AMPS)n‐RF/MAP and /AP composites were found to give the homoaldol condensation products of MAP and AP, respectively. In contrast, the corresponding non‐fluorinated AMPS oligomer/MAP and sulfuric acid/MAP composites could not give the homoaldol product at all under similar conditions. This suggests that the RF‐(AMPS)n‐RF oligomer could provide the suitable fluorinated oligomeric gel newtwok cores to interact with MAP or AP as a guest molecule, and the homoaldol condensation of encapsulated MAP and AP should proceed smoothly in the fluorinated oligomeric gel network cores. The RF‐(AMPS)n‐RF/ABP and /AMN composites could not give the homoaldol products at all under similar conditions, indicating that the more bulky aromotic ketones than MAP or AP are not likely to be encapasulated as guest molecules into the fluorinated AMPS oligomeric gel netwok cores. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   
967.
While the functional renormalization group is a powerful theoretical method, the static approximation has been usually adopted in which the Matsubara frequency dependence of vertex functions is ignored. We propose a formalism beyond the static approximation with an efficient parameterization in the Matsubara frequency space for the vertex functions to incorporate the self-energy.  相似文献   
968.
969.
2-Fluoro-3-phenyl-allyltrimethylsilane, prepared from β-fluorinated allylic acetate via a π-allylpalladium intermediate, reacted with various aldehydes and acetals in the presence of TiCl4 to afford the corresponding homoallyl alcohols and homoallyl ethers, respectively, in good to moderate yields.  相似文献   
970.

Background  

The peptide gurmarin is a selective sweet response inhibitor for rodents. In mice, gurmarin sensitivity differs among strains with gurmarin-sensitive C57BL and gurmarin-poorly-sensitive BALB strains. In C57BL mice, sweet-responsive fibers of the chorda tympani (CT) nerve can be divided into two distinct populations, gurmarin-sensitive (GS) and gurmarin-insensitive (GI) types, suggesting the existence of two distinct reception pathways for sweet taste responses. By using the dpa congenic strain (dpa CG) whose genetic background is identical to BALB except that the gene(s) controlling gurmarin sensitivity are derived from C57BL, we previously found that genetically-elevated gurmarin sensitivity in dpa CG mice, confirmed by using behavioral response and whole CT nerve response analyses, was linked to a greater taste cell population co-expressing sweet taste receptors and a Gα protein, Gα-gustducin. However, the formation of neural pathways from the increased taste cell population to nerve fibers has not yet been examined.  相似文献   
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