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101.
Yuta Saga Yuka Mino Shin-ichi Kawaguchi Daoqing Han Akiya Ogawa Li-Biao Han 《Tetrahedron: Asymmetry》2017,28(1):84-89
A variety of P-stereogenic organophosphorus compounds can be readily prepared by stereoretentive addition. The PMe3-catalyzed addition of optically active (?)MenthylO(Ph)P(O)H compounds to electron deficient alkenes occur stereospecifically, to produce the corresponding P-stereogenic adducts in high yields. By simply removing the volatiles under vacuum, spectroscopically pure products can be obtained. The present method provides a salt-free clean process for the preparation of P-chiral organophosphorus compounds. 相似文献
102.
Hirohito Kan Tosiaki Miyati Harumasa Kasai Nobuyuki Arai Naoki Ohno Mitsuhito Mase Yuta Shibamoto 《Magnetic resonance imaging》2014
Introduction
To clarify the mechanism underlying apparent diffusion coefficient (ADC) changes in regional intracranial tissue during the cardiac cycle, we investigated relationships among ADC changes, volume loading, and intracranial pressure using a hemodialyzer phantom in magnetic resonance imaging (MRI).Materials and Methods
The hemodialyzer phantom consisted of hollow fibers (HF), the external space of HFs (ES), and a gateway of dialysis solution, filled with syrup solution and air. The high-volume and low-volume loadings were periodically applied to HFs by a to-and-fro flow pump, and syrup solution was permitted to enter or leave HFs during the volume loading cycles. ADC maps at each volume loading phase were obtained using ECG-triggered single-shot diffusion echo-planar imaging. Dynamic phase contrast MRI was also used to measure volume loading to the phantom. We compared the ADC changes, volume loading, and intracranial pressure in the phantom during the cardiac cycle.Results
ADC changes synchronized significantly with absolute volumetric flow rate change. The maximum ADC change was higher in high-volume loading cycles than in low-volume loading cycles. Results showed that the water molecules in ES fluctuated according to the force transferred from HF to ES. ADC changes were dependent upon the volumetric flow rate during the cardiac cycle.Conclusions
Our original phantom allowed us to clarify the mechanism underlying water fluctuations in intracranial tissues. Measurement of maximum changes in ADC is an effective method to define the transfer characteristics of the arterial pulsatile force in regional intracranial tissue. 相似文献103.
Wong CP Shimada M Nagakura Y Nugroho AE Hirasawa Y Kaneda T Awang K Hadi AH Mohamad K Shiro M Morita H 《Chemical & pharmaceutical bulletin》2011,59(3):407-411
Five new limonoids, ceramicines E-I (1-5), have been isolated from the bark of Chisocheton ceramicus. The structures and relative stereochemistry of them were fully elucidated based on 1D- and 2D-NMR data. Ceramicines E-I (1-5) exhibited moderate cell growth inhibitory activities on a range of cell lines (HL-60, A549, MCF7, and HCT116). The absolute structure of previously isolated ceramicine B (6) was also elucidated by circular dichroism (CD) and X-ray analysis. 相似文献
104.
Yuta Yanagita Hugh Nakamura Kenji Shirokane Yusuke Kurosaki Dr. Takaaki Sato Prof. Dr. Noritaka Chida 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(2):678-684
While the synthesis of amide bonds is now one of the most reliable organic reactions, functionalization of amide carbonyl groups has been a long‐standing issue due to their high stability. As an ongoing program aimed at practical transformation of amides, we developed a direct nucleophilic addition to N‐alkoxyamides to access multisubstituted amines. The reaction enabled installation of two different functional groups to amide carbonyl groups in one pot. The N‐alkoxy group played important roles in this reaction. First, it removed the requirement for an extra preactivation step prior to nucleophilic addition to activate inert amide carbonyl groups. Second, the N‐alkoxy group formed a five‐membered chelated complex after the first nucleophilic addition, resulting in suppression of an extra addition of the first nucleophile. While diisobutylaluminum hydride (DIBAL‐H) and organolithium reagents were suitable as the first nucleophile, allylation, cyanation, and vinylation were possible in the second addition including inter‐ and intramolecular reactions. The yields were generally high, even in the synthesis of sterically hindered α‐trisubstituted amines. The reaction exhibited wide substrate scope, including acyclic amides, five‐ and six‐membered lactams, and macrolactams. 相似文献
105.
Photochemical energy transfer was examined on the flat clay surface. By the change of surrounding atmosphere, the molecular adsorption orientation angle of dyes can be modulated. It is turned out that the energy transfer efficiency between dyes can be controlled by the relative orientation change between dyes. The change of orientation factor and spectral overlap factor was the main factor to affect the energy transfer efficiency. This technique would be useful to construct the photo-functional materials such as chromic and light harvesting system. 相似文献
106.
Double cellular detonations were numerically investigated using two-dimensional Euler equations with two successive chemical reactions, whose reaction lengths differ one order of magnitude. Simulated soot track images showed the double cellular structure with two cell widths that differ one order of magnitude, as well as previous experiments and numerical simulations. We successfully divided the double cellular detonation with two successive exothermic reactions into two detonations, primary and secondary detonations, with a single exothermic reaction, based on p–v relation of Rayleigh line and Hugoniot curves with the addition of the hypothetical condition of intermediate initial state. The ratio of cell widths of primary and secondary detonations showed good agreement with that caused by the first and second reactions of double cellular detonation, and there was no interaction between two successive chemical reactions. The linear stability analysis of planar detonation and the soot rack images of double, primary and secondary detonations showed that instabilities of primary and secondary detonations are dominant to that of double cellular detonation with two successive reactions. We confirmed the validity of division of two successive reactions to clarify the detonation instability and its cellular structure. 相似文献
107.
Site-specific electron transport phenomena through benzene and benzenedithiol derivatives are discussed on the basis of a qualitative Hu?ckel molecular orbital analysis for better understanding of the effect of anchoring sulfur atoms. A recent work for the orbital control of electron transport through aromatic hydrocarbons provided an important concept for the design of high-conductance connections of a molecule with anchoring atoms. In this work the origin of the frontier orbitals of benzenedithiol derivatives, the effect of the sulfur atoms on the orbitals and on the electron transport properties, and the applicability of the theoretical concept on aromatic hydrocarbons with the anchoring units are studied. The results demonstrate that the orbital view predictions are applicable to molecules perturbed by the anchoring units. The electron transport properties of benzene are found to be qualitatively consistent with those of benzenedithiol with respect to the site dependence. To verify the result of the Hu?ckel molecular orbital calculations, fragment molecular orbital analyses with the extended Hu?ckel molecular orbital theory and electron transport calculations with density functional theory are performed. Calculated results are in good agreement with the orbital interaction analysis. The phase, amplitude, and spatial distribution of the frontier orbitals play an essential role in the design of the electron transport properties through aromatic hydrocarbons. 相似文献
108.
Remina Otsuka Prof. Dr. Keisuke Hirata Yuta Sasaki Prof. Dr. James M. Lisy Prof. Dr. Shun-ichi Ishiuchi Prof. Dr. Masaaki Fujii 《Chemphyschem》2020,21(8):712-724
The infrared (IR) spectra of alkali and alkaline earth metal ion complexes with the Ac-Tyr-NHMe (GYG) peptide have been measured by laser photodissociation in a cold ion trap coupled with an electrospray mass spectrometer. The GYG peptide corresponds to a portion of the ion selectivity filter in the KcsA K+ channel that allows K+ to pass, but blocks Na+ even though it has a smaller ionic radius than K+. This current study extends a previous investigation on Na+ and K+ to the entire set of alkali metaI ions and alkaline earth dications. IR-IR hole-burning (IR2 dip) spectroscopy has established the coexistence of several conformers of the GYG-metal ion complexes. The structures of the conformers were assigned by comparison between the isomer-selected IR spectra and theoretical IR spectra obtained from quantum chemical calculations. It was found that the structure of the dominant conformer correlates with the ability of the ion to permeate through the K+ channel. 相似文献
109.
Elucidation of Pseurotin Biosynthetic Pathway Points to Trans‐Acting C‐Methyltransferase: Generation of Chemical Diversity
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Dr. Yuta Tsunematsu Manami Fukutomi Dr. Takayoshi Saruwatari Prof. Dr. Hiroshi Noguchi Prof. Dr. Kinya Hotta Prof. Dr. Yi Tang Prof. Dr. Kenji Watanabe 《Angewandte Chemie (International ed. in English)》2014,53(32):8475-8479
Pseurotins comprise a family of structurally related Aspergillal natural products having interesting bioactivity. However, little is known about the biosynthetic steps involved in the formation of their complex chemical features. Systematic deletion of the pseurotin biosynthetic genes in A. fumigatus and in vivo and in vitro characterization of the tailoring enzymes to determine the biosynthetic intermediates, and the gene products responsible for the formation of each intermediate, are described. Thus, the main biosynthetic steps leading to the formation of pseurotin A from the predominant precursor, azaspirene, were elucidated. The study revealed the combinatorial nature of the biosynthesis of the pseurotin family of compounds and the intermediates. Most interestingly, we report the first identification of an epoxidase C‐methyltransferase bifunctional fusion protein PsoF which appears to methylate the nascent polyketide backbone carbon atom in trans. 相似文献
110.
Enantioselective Synthesis of [9]‐ and [11]Helicene‐like Molecules: Double Intramolecular [2+2+2] Cycloaddition
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Yuki Kimura Naohiro Fukawa Yuta Miyauchi Prof. Dr. Keiichi Noguchi Prof. Dr. Ken Tanaka 《Angewandte Chemie (International ed. in English)》2014,53(32):8480-8483
The enantioselective synthesis of completely ortho‐fused [9]‐ and [11]helicene‐like molecules has been achieved through a rhodium‐mediated, intramolecular, double [2+2+2] cycloaddition of phenol‐ or 2‐naphthol‐linked hexaynes. Crystal structures and photophysical properties of these [9]‐ and [11]helicene‐like molecules have also been disclosed. 相似文献