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11.
12.
Tetsuji Sugata Yoko Kan Yoshiteru Nagaregawa Tomofumi Miyamoto Ryuichi Higuchi 《Journal of carbohydrate chemistry》2013,32(6):917-925
Abstract The hematoside analog 1 [NeuGcα(2→3)Galβ(1→4)Glcβ(1→1)Cer], which contains a phytosphingosine as a sphingoid base and an α-hydroxyfatty acid, has been synthesized. Coupling of the methyl (methyl 5-benzyloxyacetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-2-thio-D-glycero-α- and -β-D-galacto-2-nonulopyranosid)onate 5, prepared from the corresponding 5-acetamido derivative 2, with a lactose derivative 6 afforded sialolactoside 7, which was converted to the corresponding trichloroacetimidate 10. Glycosylation of 10 with the ceramide tribenzoate 12 gave the protected hematoside analog 13, which was deprotected to the hematoside analog 1. 相似文献
13.
We propose and demonstrate generation of an in-phase optical pulse train from an optical beat signal. The proposed method is based on four-wave mixing occurring between the two continuous waves of the beat signal and on spectral filtering to shape the spectrum to be symmetric about the carrier frequency. We perform an experiment to verify the proposed method and obtain a 1.5 ps width in-phase pulse train from a 160 GHz beat signal. Furthermore, we employ a pulse compression scheme to reshape and compress the obtained pulse train, and we show that a 160 GHz repeating, 0.7 ps FWHM, nearly transform-limited, in-phase sech pulse train is successfully generated. 相似文献
14.
Main mesomorphic properties of cellulose and cello- and chito-oligosaccharide derivatives are overviewed, and their structuring principles are briefly discussed with some new analyses incorporated. 相似文献
15.
Masahiko Minoda Katsushi Yamaoka Kenji Yamada Akira Takaragi Takeaki Miyamoto 《Macromolecular Symposia》1995,99(1):169-177
The present paper focuses on (i) a new synthetic methodology to prepare vinyl ether-based synthetic glycoconjugates (glycopolymers) with well-controlled structure, and on (ii) the application of glycopolymers bearing modified disaccharide residue as thermotropic liquid crystalline (LC) materials. Two vinyl ethers (VEs) having pendant glucose residues with their hydroxyl functions protected by acetyl and isopropylidene groups, respectively, were found to undergo living cationic polymerization initiated by a HI/ZnI2-initiating system. Deprotection of the resultant monodisperse polymers led to water-soluble polymers bearing a pendant glucose residue. Sequential living block copolymerization of glucose-containing VE and alkyl VE, and subsequent deprotection afforded an amphiphilic block copolymer of well-controlled structure. Transmission electron microscopic observation of its cast thin film revealed microphase-separated surface morphologies that varied with varying segment composition ratio. A VE substituted with a heptadecanoated cellobiose pendant was independently prepared, and was cationically polymerized to give a thermotropic LC polymer. From X-ray analysis, the mesophase was assigned to a discotic columnar in type, in which each main chain, extended due to the steric repulsion between the neighboring bulky pendants, was surrounded by three discotic columns. 相似文献
16.
Widely tunable terahertz (THz)-wave generation using difference frequency generation (DFG) in an organic N-benzyl-2-methyl-4-nitroaniline (BNA) crystal was demonstrated. To our knowledge, this is the first report of THz-wave generation by BNA DFG. Large, high-quality single crystals of BNA (phi 8 mm x 30 mm) were grown using the vertical Bridgman method. The nonlinear optical (NLO) coefficient d(33) of the BNA crystal is approximately 234 pm/V, which is the largest value reported for any yellow NLO material. The collinear phase-matching condition of the type-0 configuration is satisfied using a 0.7-1 microm band pump wavelength. We generated THz waves using an organic BNA crystal; the generation range is 0.1-15 THz. 相似文献
17.
Yulu Jiang Dr. Taro Ozaki Mei Harada Tadachika Miyasaka Dr. Hajime Sato Dr. Kazunori Miyamoto Dr. Junichiro Kanazawa Dr. Chengwei Liu Prof. Dr. Jun-ichi Maruyama Dr. Masaatsu Adachi Dr. Atsuo Nakazaki Prof. Dr. Toshio Nishikawa Prof. Dr. Masanobu Uchiyama Dr. Atsushi Minami Prof. Dr. Hideaki Oikawa 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(41):18152-18158
Lolitrems are tremorgenic indole diterpenes that exhibit a unique 5/6 bicyclic system of the indole moiety. Although genetic analysis has indicated that the prenyltransferase LtmE and the cytochrome P450 LtmJ are involved in the construction of this unique structure, the detailed mechanism remains to be elucidated. Herein, we report the reconstitution of the biosynthetic pathway for lolitrems employing a recently established genome-editing technique for the expression host Aspergillus oryzae. Heterologous expression and bioconversion of the various intermediates revealed that LtmJ catalyzes multistep oxidation to furnish the lolitrem core. We also isolated the key reaction intermediate with an epoxyalcohol moiety. This observation allowed us to establish the mechanism of radical-induced cyclization, which was firmly supported by density functional theory calculations and a model experiment with a synthetic analogue. 相似文献
18.
Hisahiro Nakayama Jiro Kasahara Akiko Matsuo Ikkoh Funaki 《Proceedings of the Combustion Institute》2013,34(2):1939-1947
The propagation of curved detonation waves of gaseous explosives stabilized in rectangular-cross-section curved channels is investigated. Three types of stoichiometric test gases, C2H4 + 3O2, 2H2 + O2, and 2C2H2 + 5O2 + 7Ar, are evaluated. The ratio of the inner radius of the curved channel (ri) to the normal detonation cell width (λ) is an important factor in stabilizing curved detonation waves. The lower boundary of stabilization is around ri/λ = 23, regardless of the test gas. The stabilized curved detonation waves eventually attain a specific curved shape as they propagate through the curved channels. The specific curved shapes of stabilized curved detonation waves are approximately formulated, and the normal detonation velocity (Dn)?curvature (κ) relations are evaluated. The Dn nondimensionalized by the Chapman–Jouguet (CJ) detonation velocity (DCJ) is a function of the κ nondimensionalized by λ. The Dn/DCJ?λκ relation does not depend on the type of test gas. The propagation behavior of the stabilized curved detonation waves is controlled by the Dn/DCJ?λκ relation. Due to this propagation characteristic, the fully-developed, stabilized curved detonation waves propagate through the curved channels while maintaining a specific curved shape with a constant angular velocity. Self-similarity is seen in the front shock shapes of the stabilized curved detonation waves with the same ri/λ, regardless of the curved channel and test gas. 相似文献
19.
Daisuke Sawai Mika Miyamoto Tetsuo Kanamoto Masayoshi Ito 《Journal of Polymer Science.Polymer Physics》2000,38(19):2571-2579
No systematic study has been reported on the lamellar thickening in atactic poly(acrylonitrile) (PAN) upon annealing because PAN, in the form of solution‐cast films or their drawn products, generally shows no small‐angle X‐ray scattering (SAXS) maximum corresponding to the lamellar thickness. In this work, PAN crystals were precipitated during the thermal polymerization of acrylonitrile in solution. The nascent PAN film, obtained by the filtration of the crystal suspension, exhibited a clear SAXS maximum revealing the lamellar structure. The lamellar thickening upon annealing of the nascent PAN films was studied in the temperature range 100–180 °C, where the degradation was minimal, as confirmed by the absence of an IR absorption band at 1605 cm−1 ascribed to the cyclized nitrile groups. Above 190 °C, the degradation of the samples was significant, and the SAXS became too broad to determine the scattering maximum. The long period was significantly affected by the annealing time (ta) and the temperature (Ta). Depending on ta, three stages were observed for the lamellar thickening behavior. The lamellar thickness stayed constant in stage I (ta = 0.5–3 min, depending on Ta), rapidly increased in stage II (ta = 0.5–8 min), and stayed at a constant value characteristic for each Ta at yet longer ta's in stage III. The lamellar thickness characteristic for Ta increased rapidly with increasing Ta at 165 °C (or higher), which was 152 °C lower than the estimated melting temperature of PAN (Tm = 317 °C). A possible mechanism for such lamellar thickening in PAN far below the Tm is discussed on the basis of the enhanced chain mobility in the crystalline phase above the crystal/crystal reversible transition at 165–170 °C detected by differential scanning calorimetry and wide‐angle X‐ray diffraction. The structural changes associated with annealing are also discussed. © 2000 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 38: 2571–2579, 2000 相似文献
20.
Nakata Y Honda Y Ninomiya S Seki T Aoki T Matsuo J 《Journal of mass spectrometry : JMS》2009,44(1):128-136
The importance of imaging mass spectrometry (MS) for visualizing the spatial distribution of molecular species in biological tissues and cells is growing. We have developed a new system for imaging MS using MeV ion beams, termed MeV-secondary ion mass spectrometry (MeV-SIMS) here, and demonstrated more than 1000-fold increase in molecular ion yield from a peptide sample (1154 Da), compared to keV ion irradiation. This significant enhancement of the molecular ion yield is attributed to electronic excitation induced in the near-surface region by the impact of high energy ions. In addition, the secondary ion efficiency for biologically important compounds (>1 kDa) increased to more than 10(10) cm(-2), demonstrating that the current technique could, in principle, achieve micrometer lateral resolution. In addition to MeV-SIMS, peptide compounds were also analyzed with cluster-SIMS and the results indicated that in the former method the molecular ion yields increased substantially compared to the latter. To assess the capability of MeV-SIMS to acquire heavy-ion images, we have prepared a micropatterned peptide surface and successfully obtained mass spectrometric imaging of the deprotonated peptides (m/z 1153) without any matrix enhancement. The results obtained in this study indicate that the MeV-SIMS technique can be a powerful tool for high-resolution imaging in the mass range from 100 to over 1000 Da. 相似文献