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61.
Shogo Mitsuhashi Junko Kawai Tomofumi Santa Toshimasa Toyo’oka 《Analytica chimica acta》2006,562(1):36-43
Kynurenic acid (KYNA), an endogenous antagonist of ionotropic glutamate and α7 nicotinic receptors, was fluorometrically determined by column-switching high-performance liquid chromatography (HPLC) with fluorescence detection. The HPLC system consists of two octadecyl silica (ODS) columns, both of which are connected with an anion-exchange column (trapping column). Following sample injection onto the HPLC column, KYNA was separated on the first ODS column with a mobile phase of H2O/acetonitrile (95/5) containing 0.1% acetic acid. The peak fraction of KYNA was trapped on the anion-exchange column by changing the position of a six-port valve and then introduced into the second ODS column. Subsequently, KYNA was detected fluorometrically as a fluorescence complex formed with zinc ion which was pumped constantly. Instrumental limit of detection was approximately 0.16 nM, which corresponded to 8.0 fmol (per 50 μl injection, signal to noise ratio 3), and the limit of quantification was 0.53 nM (signal to noise ratio 10). Intra- and inter-day relative standard deviations were 1.1-3.9% (n = 3) and 3.0-5.3% (n = 3), respectively. The peak of KYNA in rat plasma was clearly detected by the proposed column-switching HPLC system after a facile pretreatment procedure. Intra- and inter-day relative mean errors were −1.6-1.4% (n = 3) and −2.4 to −0.4% (n = 3), respectively, with a satisfactory precision (within 5.0%). A calibration curve for the determination of KYNA showed a good linearity (r2 > 0.999) in the range of 25-200 nM. The KYNA concentrations in the plasma of male Sprague-Dawley rats (8-week-old) were 44 ± 5.5 nM (mean ± S.E., n = 5). In ketamine-treated rats, which are animal models of schizophrenia, the plasma KYNA concentrations were significantly increased compared with those in the control rats (p < 0.05). 相似文献
62.
63.
The phase-matched second harmonic generation by periodic structures composed of laminae of nonlinear optical crystals has been studied experimentally. It is shown that the intensity of the second harmonic is approximately proportional to the square of the number of laminae under phase-matched condition, which is satisfied over a broad frequency range by the variation of the angle of incidence when a laminar structure with a period much larger than the coherence length is used. 相似文献
64.
Direct Transformation of Molecular Dinitrogen into Ammonia Catalyzed by Cobalt Dinitrogen Complexes Bearing Anionic PNP Pincer Ligands 下载免费PDF全文
Dr. Shogo Kuriyama Dr. Kazuya Arashiba Prof. Dr. Hiromasa Tanaka Yuki Matsuo Dr. Kazunari Nakajima Prof. Dr. Kazunari Yoshizawa Prof. Dr. Yoshiaki Nishibayashi 《Angewandte Chemie (International ed. in English)》2016,55(46):14291-14295
The direct formation of ammonia from molecular dinitrogen under mild reaction conditions was achieved by using new cobalt dinitrogen complexes bearing an anionic PNP‐type pincer ligand. Up to 15.9 equivalents of ammonia were produced based on the amount of catalyst together with 1.0 equivalent of hydrazine (17.9 equiv of fixed nitrogen atoms). 相似文献
65.
66.
Prof. Hidemitsu Uno Kota Muramatsu Shogo Hiraoka Hiroyuki Tahara Mako Hirose Eidai Tamura Tatsumi Shiraishi Dr. John Mack Prof. Nagao Kobayashi Dr. Shigeki Mori Dr. Tetsuo Okujima Dr. Masayoshi Takase 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(25):5701-5708
A bicyclo[2.2.2]octadiene(BCOD)-fused bis(dipyrromethane) derivative was reacted with methylal in the presence of trifluoroacetic acid followed by oxidation with chloranil to give a doubly N-confused phlorin derivative, which did not undergo the retro-Diels–Alder reaction extruding an ethylene molecule on heating. In contrast, a 7-tert-butoxybicyclo[2.2.1]heptadiene(7-BuOBCHD)-fused bis(dipyrromethane) yielded benzene-ring-fused doubly N-confused porphyrins by following similar reaction sequences. 相似文献
67.
Shuntaro Mataka Kazufumi Takahashi Masashi Tashiro Wei-Hua Lin Shin-Ichi Iwasaki Tetsuo Tsutsui Shogo Saito Shinji Akiyama Tadashi Yonemitsu 《Journal of heterocyclic chemistry》1989,26(1):215-219
Reversible color change of 4,6,7-tri(alkoxy-substituted phenyl)-1,2,5-thiadiazolo[3,4-c]pyridines 5 in the solid state was observed: on grinding, yellow crystals of 5 became an orange amorphous solid which, on heating or washing with an appropriate solvent, gave the original yellow crystals. 相似文献
68.
Masahiro Hayashi Shogo Tawada Yoshihiro Kubota Yoshihiro Sugi Jong Ho Kim 《Reaction Kinetics and Catalysis Letters》2004,83(2):329-335
Although extensive isomerization of 4,4'-diisopropylbiphenyl (4,4'-DIPB) occurred at 300oC over H-mordenite, high selectivity for 4,4'-DIPB among DIPB isomers was observed over silica-modified H-mordenite. This
is due to the prevention of the isomerization of 4,4'-DIPB by the deactivation of external acid sites.
This revised version was published online in June 2006 with corrections to the Cover Date. 相似文献
69.
N-Isobutylidenemethylamine reacted with dimethyl methoxymethylenemalonate to afford the N-alkylation product 3a exclusively. Exchanging the N-substituent of the Schiff's base from methyl to t-butyl altered the course of the reaction, allowing Michael addition to take place predominantly. The Michael adduct 4c on reaction with hydrazinoalkanols 6a,b, 6c,d and 6e gave tetrahydropyrazolo[5,1-b]oxazoles 9a,b , tetrahydro-pyrazolo[5,1-b][1,3]oxazines 9c,d and hexahydropyrazolo[5,1-b][1,3]oxazepine 9e , respectively. 相似文献
70.
A convenient and environmentally-friendly synthetic method of olefins via deacylation reaction is described. The reaction gives olefins by condensation of aldehydes with a variety of 1,3-dicarbonyl compounds in the presence of anhydrous potassium carbonate at room temperature in high yields (70-90%) in one step. The synthetic potential of this strategy can be used as an alternative procedure to the Wittig, Wittig-Horner reactions. The stereochemistry of the resulted olefins was determined by NOE experiment with correct radio frequency and X-ray analysis. The E/Z selectivity of the deacylation reaction depends on the α-substituents of the 1,3-dicarbonyl compounds. 相似文献