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51.
Hiroki FurutaToyohisa Takase Hisafumi HayashiRyoji Noyori Yuji Mori 《Tetrahedron》2003,59(49):9767-9777
An efficient method has been developed for the synthesis of trans-fused tetrahydropyrans with angular methyl groups adjacent to the ring oxygen. The procedure involves the coupling reaction of a sulfonyl-stabilized oxiranyl anion with an appropriate triflate followed by 6-endo cyclization, and is effective for the construction of 6/6- and 6/7/6-cyclic ether ring systems with sterically congested 1,3-diaxial methyl groups. 相似文献
52.
Hiroyuki?OhshimaEmail author Hiroko?Sato Hiroki?Matsubara Atsushi?Hyono Masayoshi?Okubo 《Colloid and polymer science》2004,282(10):1174-1178
A theory of adsorption kinetics with time delay [Ohshima et al. (1992) Colloid Polym. Sci. 270:707] is developed and applied to the surface tension of a polymer solution. It is found that the general appearance of the overshoot and oscillation in the time course of the surface tension of aqueous gelatin solution observed by Sato and Ueberreiter [(1979) Makromol. Chem. 180:829, 1107; (1979) Polym. Prepr. Am. Chem. Soc. Div. Polym. Chem. 20:907) can be explained by the present theory. 相似文献
53.
A series of samples with the composition Ca(1)(-)(x)Na(2)(x)Al(2)B(2)O(7) (0 < x < or = 1) was investigated and a hexagonal structure with unusually large range of homogeneity (at least from x = 0.01 to 0.95) was revealed. The hexagonal phase consists of [Al(2)B(2)O(7)](infinity)(2)(-) lamellae stacked along the c axis, as in CaAl(2)B(2)O(7) and Na(2)Al(2)B(2)O(7). Nevertheless, the configuration and stacking sequence of the [Al(2)B(2)O(7)](infinity)(2)(-) lamellae are different in these three structures. In the hexagonal structure of Ca(1)(-)(x)()Na(2)(x)()Al(2)B(2)O(7), Ca and half Na cations (Na1) statistically occupy the same crystallographic site which is located between the [Al(2)B(2)O(7)](infinity)(2)(-) lamellae, the other half Na cations (Na2) distribute in the planes bisecting the [Al(2)B(2)O(7)](infinity)(2)(-) lamellae. Depending on the composition, the site occupation factor of Na2 site can vary in the same range as x, leading to a tunable density of Na(+) vacancies in the structure. The AlO(4) tetrahedra and BO(3) triangles in the structure tilt in appropriate ways to improve the bond valence sum of Na2 cations which are not sufficiently bonded to the anions. 相似文献
54.
我们利用具有不同对称性的同分异构体,通过改变分子间氢键网络,操控单链磁体行为,成功合成了2例化合物:[NiⅡ(L1)][FeⅢ(Tp)(CN)3]2·3.5H2O (1)和[NiⅡ(L2)][FeⅢ(Tp)(CN)3]2·3H2O (2),其中Tp=hydrotris (pyrazolyl) borate,L1=3,4-bis (1H-imid-azol-1-yl) thiophen,L2=1,2-bis (1H-imidazol-1-yl) thiophen)。磁性研究表明,1和2表现为具有不同矫顽场的单链磁体行为。1的矫顽场为8.41 kOe,而2的矫顽场为3.84 kOe。 相似文献
55.
Paul Grocki Mark Woollam Luqi Wang Shengzhi Liu Maitri Kalra Amanda P. Siegel Bai-Yan Li Hiroki Yokota Mangilal Agarwal 《Molecules (Basel, Switzerland)》2022,27(13)
Volatile organic compounds (VOCs) in urine are potential biomarkers of breast cancer. Previously, our group has investigated breast cancer through analysis of VOCs in mouse urine and identified a panel of VOCs with the ability to monitor tumor progression. However, an unanswered question is whether VOCs can be exploited similarly to monitor the efficacy of antitumor treatments over time. Herein, subsets of tumor-bearing mice were treated with pitavastatin at high (8 mg/kg) and low (4 mg/kg) concentrations, and urine was analyzed through solid-phase microextraction (SPME) coupled with gas chromatography-mass spectrometry (GC-MS). Previous investigations using X-ray and micro-CT analysis indicated pitavastatin administered at 8 mg/kg had a protective effect against mammary tumors, whereas 4 mg/kg treatments did not inhibit tumor-induced damage. VOCs from mice treated with pitavastatin were compared to the previously analyzed healthy controls and tumor-bearing mice using chemometric analyses, which revealed that mice treated with pitavastatin at high concentrations were significantly different than tumor-bearing untreated mice in the direction of healthy controls. Mice treated with low concentrations demonstrated significant differences relative to healthy controls and were reflective of tumor-bearing untreated mice. These results show that urinary VOCs can accurately and noninvasively predict the efficacy of pitavastatin treatments over time. 相似文献
56.
Ionic liquids (ILs) are salts with an extremely low melting point. Substantial efforts have been made to address their low melting point from the enthalpic standpoint (i.e. interionic interactions). However, this question is still open. In this study, we report our findings that entropic (large fusion entropy), rather than enthalpic, contributions are primarily responsible for lowering the melting point in many cases, based on a large thermodynamic dataset. We have established a computational protocol using molecular dynamics simulations to decompose fusion entropy into kinetic (translational, rotational, and intramolecular vibrational) and structural (conformational and configurational) terms and successfully applied this approach for two representatives of ILs and NaCl. It is revealed that large structural contribution, particularly configurational entropy in the liquid state, plays a deterministic role in the large fusion entropy and consequently the low melting point of the ILs.Large structural entropy makes salts liquid at room temperature. 相似文献
57.
Dr. Tatsuya Takimoto Prof. Hideaki Sasaki Prof. Hirohito Tsue Dr. Hiroki Takahashi Prof. Alexander D. MacKerell Jr. Ayumi Nakamura Katsuya Nakano Eori Okazaki Tatsuki Betsuyaku Ryosuke Tachibana Dr. Kazuhito Hioki Dr. Ozge Yoluk Dr. Sunhwan Jo 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(5):1648-1654
A simple approach to the synthesis of heterocyclophane consisting of two 4,4’-bithiazoles has been developed in mild conditions. The heterocyclophane with two short chains was conveniently prepared by Hantzsch thiazoles synthesis using the reaction of 3-tert-butoxycarbonyl-3-azapentanethiocarboxamide with 1,4-dibromobutane-2,3-dione in methanol under reflux for only 15 min. Amino groups at the linkers of this heterocyclophane can be functionalized to give acylated and carbamate derivatives. Their properties as protein kinase inhibitors were investigated, and one of the heterocyclophanes exhibited specific anti-activity for c-mesenchymal epithelial transition factor (IC50=603 nm ), among seven types of protein kinases investigated. The computational site identification by ligand competitive saturation method was used to determine why the one heterocyclophane exhibited strong anti-activity for c-mesenchymal epithelial transition factor. 相似文献
58.
A novel method for determination of inorganic oxyanions by electrospray ionization mass spectrometry using dehydration reactions
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Hirochika Kojima Shota Kurihara Yoshito Watanabe Koki Iwamaru Kiichi Sato Kin‐ichi Tsunoda Hiroki Hotta 《Journal of mass spectrometry : JMS》2016,51(2):123-131
Novel methods for the determination of inorganic oxyanions by electrospray (ES) ionization mass spectrometry have been developed using dehydration reactions between oxyanions and carboxylic acids at the ES interface. Twelve oxyanions (VO3?, CrO42?, MoO42?, WO42?, BO33?, SiO32?, SiO44?, AsO44?, AsO2?, SeO42?, SeO32? and NO2?), out of 16 tested, reacted with at least one of four aminopolycarboxylic acids, i.e. iminodiacetic acid (IDA), nitrilotriacetic acid (NTA), trans‐1,2‐diaminocyclohexane‐N,N,N′,N′‐tetraacetic acid and triethylenetetramine‐N,N,N′,N″,N′″,N′″‐hexaacetic acid, at the ES interface to produce the dehydration products that gave intense mass ion responses, sufficient for trace analysis. As examples, trace determinations of CrVI and silica in water samples were achieved after online ion exchange chromatography, where the dehydration product of CrO42? and NTA (m/z 290) and that of SiO44? and IDA (m/z 192) were measured. The limits of detection of the respective methods were 17 nM (0.83 ng Cr/ml) for CrVI and 0.17 μM (4.8 ng Si/mL) for SiO44?. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
59.
Shigekazu Ito Hiroki Sugiyama Masaaki Yoshifuji 《Phosphorus, sulfur, and silicon and the related elements》2013,188(4-5):785-788
1-(2,4,6-Tri-tert-butylphenyl)-2-phosphaethyne (1) was allowed to react with 0.5 equiv of an alkyllithium and subsequently with an alcohol to afford a bulky 1,3-diphosphacyclobutene, and its structure and coordination properties on transition metals were investigated. On the other hand, 1 was allowed to react with an alkyllithium and iodomethane to form a stable biradical, 1,3-diphosphacyclobutane-2,4-diyl. 相似文献
60.