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排序方式: 共有786条查询结果,搜索用时 31 毫秒
1.
Haruki Inoue Dr. Shin-ichi Naya Atsunobu Akita Dr. Hisashi Sugime Prof. Dr. Hiroaki Tada 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(46):e202201653
Gold nanoparticles with different mean sizes were formed on antimony-doped tin oxide nanocrystals by the temperature-varied deposition-precipitation method (Au/ATO NCs). Au/ATO NCs possess strong absorption in the near-infrared region due to Drude excitation in addition to the localized surface plasmon resonance (LSPR) of AuNPs around 530 nm. Au/ATO NCs show thermally activated catalytic activity for the oxidation of cinnamyl alcohol to cinnamaldehyde by hydrogen peroxide. The catalytic activity increases with a decrease in the mean Au particle size (dAu) at 5.3 nm≤dAu≤8.2 nm. Light irradiation (λex >660 nm, ∼0.5 sun) of Au/ATO NCs increases the rate of reaction by more than twice with ∼95 % selectivity. Kinetic analyses indicated that the striking enhancement of the reaction stems from the rise in the temperature near the catalyst surface of ∼30 K due to the photothermal effect of the ATO NCs. 相似文献
2.
Prof. Dr. Erika Nakashima Prof. PhD Hisashi Yamamoto 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(35):e202103989
Since the global peptide drug market demand has been predicted to increase, highly efficient and inexpensive mass scale peptides are required. However, the production process raises questions about the cost of energy input, scale-up production, raw materials, and solvents treatment. This paper introduces 2 methods for the 2–4 mer oligopeptides bond formation for batch reaction utilizing 50–100 mol% of a mild Brønsted acid under the mild condition. One of the methods has been capably adapted to flow synthesis at room temperature using organic solvents with boiling points below 100 °C. The method applies the tert-butoxycarbonyl amino methoxy group, forming the desired dipeptide without solvent at mild temperatures. Furthermore, the conversion of the carboxylic acid leaving the group to phenyl ester promotes peptide bond formation, and the reaction were applied to di, tri, and tetrapeptide bond formation in excellent yield without notable racemization at ambient temperature (up to >99 % yield and 99 : 1 dr). Finally, this study proposes this new production method to overcome the limited scale-up production by reaction device scale: liquid phase biomimetic catalytic peptide flow synthesis utilizing a mild Brønsted acid. 相似文献
3.
Dr. Ramesh C. Samanta Prof. Hisashi Yamamoto 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(34):11976-11979
Electrophilic halogenation is used to produce a wide variety of halogenated compounds. Previously reported methods have been developed mainly using a reagent‐based approach. Unfortunately, a suitable “catalytic” process for halogen transfer reactions has yet to be achieved. In this study, arylamines have been found to generate an N‐halo arylamine intermediate, which acts as a highly reactive but selective catalytic electrophilic halogen source. A wide variety of heteroaromatic and aromatic compounds are halogenated using commercially available N‐halosuccinimides, for example, NCS, NBS, and NIS, with good to excellent yields and with very high selectivity. In the case of unactivated double bonds, allylic chlorides are obtained under chlorination conditions, whereas bromocyclization occurs for polyolefin. The reactivity of the catalyst can be tuned by varying the electronic properties of the arene moiety of catalyst. 相似文献
4.
Dr. Atsuto Izumiseki Prof. Dr. Hisashi Yamamoto 《Angewandte Chemie (International ed. in English)》2015,54(30):8697-8699
Selective Michael reaction of organolithium reagents to supersilyl methacrylate is reported. The method was able to control a single and double Michael addition. The successful termination of the process using the supersilyl protecting group allows for the controlled, chemoselective, and diastereoselective Michael reaction. 相似文献
5.
6.
Takahiro Matsumoto Seikou Nakamura Naoto Kojima Tomohiro Hasei Masayuki Yamashita Tetsushi Watanabe Hisashi Matsuda 《Tetrahedron letters》2017,58(36):3574-3578
From the methanolic extract of the aerial parts of Isodon japonicus, two new ent-kaurane diterpenes, isodonterpenes I and II, were isolated together with 10 known diterpenes. Their chemical structures were elucidated on the basis of chemical and physicochemical evidence. The absolute configuration of isodonterpene I was elucidated by Cu-Kα X-ray crystallographic analysis. Antimutagenic activities of the major diterpenes were evaluated by the Ames test. This study represents the first evaluation of the antimutagenic activities of ent-kaurane diterpenes. 相似文献
7.
Keisuke Akita Youhi Morii Hisashi Nakamura Takuya Tezuka Kaoru Maruta 《Proceedings of the Combustion Institute》2021,38(2):2247-2255
Two-dimensional axisymmetric numerical simulation reproduced flames with repetitive extinction and ignition (FREI) in a micro flow reactor with a controlled temperature profile with a stoichiometric n-heptane/air mixture, which have been observed in the experiment. The ignition of hot flame occurred from consumption reactions of CO that was remained in the previous cycle of FREI. Between extinction and ignition locations of hot flames, several other heat release rate peaks related to cool and blue flames were observed for the first time. After the extinction of the hot flame, cool flame by the low-temperature oxidation of n-heptane appeared first and was stabilized in a low wall temperature region. In the downstream of the stable cool flame, a blue flame by the consumption reactions of cool flame products of CH2O and H2O2 appeared. After that, the hot flame ignition occurred from the remaining CO in the downstream of the blue flame. Then after the next hot flame ignition, the blue flame was swept away by the propagating hot flame. Soon before the hot flame merged with the stable cool flame, the hot flame propagation was intensified by the cool flame. After the hot flame merged with the stable cool flame, the hot flame reacted with the incoming fresh mixture of n-C7H16 and O2. 相似文献
8.
Keitaro Tanoi Natsuko I. Kobayashi Takayuki Saito Naoko Iwata Atsushi Hirose Yoshimi Ohmae Ren Iwata Hisashi Suzuki Tomoko M. Nakanishi 《Journal of Radioanalytical and Nuclear Chemistry》2013,296(2):749-751
The time course of Mg uptake and release using intact rice plants and 28Mg as a tracer is presented. Since there is no conventional Mg tracer available, 28Mg was produced via 27Al(α, 3p)28Mg reaction using a cyclotron. Using the purified 28Mg tracer, it was found that the uptake amount of 28Mg by the rice plants increased linearly during 30 min of application. After 28Mg treatment for 90 min, the roots were sequentially washed with iced solution for 120 min. Within about 10 min, almost all of the 28Mg, that was thought to be weakly bound to the apoplast, was washed away. 相似文献
9.
Yasuhiro Kajihara Hironobu Hashimoto Hisashi Kodama Tomio Wakabayashi Ken-ichi Sato 《Journal of carbohydrate chemistry》2013,32(7):991-995
Abstract Specific inhibitors of glycosyltransferases have become of interest1 not only for investigation of carbohydrate-participating cell-surface phenomena but also for practical use such as chemotherapeutic reagents. Glycosyltransferases catalyze the transfer of glycosyl moieties from nucleotide donors to oligosaccharide acceptors. Therefore, two kinds of substrate-analog inhibitors are possible. The donor analogs have been rather well studied, but are not specific. On the other hand, glycosyltransferases have in general smct acceptor specifkity. Recently, acceptor analogs which inhibit the corresponding glycosyltransferases were reported2-5 and as expected were acceptor-specific inhibitors. 相似文献
10.