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61.
Shin-ichi Nakakita Kayo Hasehira Tomohiro Hosokawa Masaaki Tokuda Ken Izumori Kaoru Takegawa Jun Hirabayashi 《Journal of chromatography. A》2009,1216(26):5112-5115
A rare sugar is considered to be a monosaccharide rarely found in nature. To investigate their natural distribution and biological roles, a robust analytical system must be used to isolate, identify, and quantify them. Herein, we report the development of such a system that can specifically quantify and chromatographically separate four aldopentoses and eight aldohexoses tagged with 2-aminopyridine. Purified monosaccharides derivatized with a pyridylamino moiety (PA–monosaccharides) are first chromatographed over a high-performance anion-exchange resin. But, because two of the PA–aldohexoses used in this study, PA–talose and PA–idose, co-elute with the common saccharides, PA–glucose and PA–mannose, respectively, a second chromatographic step, reversed-phase high-performance liquid chromatography, is used to completely separate them. Thus, as shown by the results of this study, chromatographic separation of PA–monosaccharides is achievable and provides a quantitative measurement of common and rare isomeric aldopentoses and aldohexoses. 相似文献
62.
Iwao Omae 《应用有机金属化学》2009,23(3):91-107
Group 9 metal compounds in organic synthesis have two characteristic reactions. The first occurs because the group 9 metals have a high affinity to carbon–carbon or carbon–nitrogen π‐bonds. The first type of characteristic reactions in these group 9 metal compounds includes Pauson–Khand reactions, the Pauson–Khand‐type reactions ([2 + 2 + 1] cyclization), the other cyclizations and coupling reactions. The second occurs because the group 9 metals have a high affinity to carbonyl groups. The second type of characteristic reactions includes carbonylations such as hydroformylations, the carbonylations of methanol, amidocarbonylations and other carbonylations. The first characteristic reactions are applied for the synthesis of fine chemicals such as pharmaceuticals and agrochemicals. However, the second characteristic reactions are utilized not only for fine chemicals but also for important bulk commodity chemicals such as aldehydes, carboxylic acids and alcohols. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
63.
64.
Kazuchika Ohta Hiroshi Ema Yasue Morizumi Takuya Watanabe Tetsuya Fujimoto Iwao Yamamoto 《Liquid crystals》1990,8(3):311-330
Two novel types of transition-metal-containing liquid crystals, bis(p-n-koxydithiobenzoato)nickel(II) (abbreviated as (CnO-DTB)2Ni), and (p-n-alkoxydithiobenzoato)(p-n-alkoxyperthiobenzoato)nickel(II) (abbreviated as (CnO-DTB)(CnO-PTB)Ni), were synthesized. It was found that the (CnO-DTB)2Ni complex for n = 8 has smectic H and C mesophases, and that the (CnO-DTB)2Ni complexes for n = 4 and 8 easily transform into the corresponding monoperthio complexes, nO-PTB)Ni, by heating at temperatures between 230°C and 285°C. It was confirmed that the transformation originates from an intermolecular reaction between the (CnO-DTB)2Ni complexes at high temperatures, and that the origin of the extra sulphurs in the resulting (CnO-DTB)(CnO-PTB)Ni complexes is the neighbouring (CnO-DTB)2Ni complexes. Interestingly, each of the (CnO-DTB)(CnO-PTB)Ni complexes (n = 4 and 8), has nematic mesophase and exhibits a unique double melting behaviour via the nematic phase, which is the first example in liquid crystals. The reversible transformation between the blue smectic rod-like (CnO-DTB)2Ni complex and the red nematic Λ-like (CnO-DTB)(CnO-PTB)Ni complex is possible. 相似文献
65.
We give a decomposition formula for the zeta function of a group covering of a graph. 相似文献
66.
Kuniaki Tatsuta Hiroaki Tanaka Hitomi Tsukagoshi Takafumi Kashima Seijiro Hosokawa 《Tetrahedron letters》2010,51(42):5546-5549
The total synthesis of lactonamycin has been achieved. The synthesis includes sequential intramolecular conjugate addition of alcohols to the acetylenic ester, stereoselective glycosylation of the tertiary alcohol, and Michael-Dieckmann type cyclization with the thioester, by which the highly convergent route has been established. 相似文献
67.
68.
Ryota Seto Takashi Sato Takahiro Kojima Katsumoto Hosokawa Yasuhito Koyama Gen‐Ichi Konishi Toshikazu Takata 《Journal of polymer science. Part A, Polymer chemistry》2010,48(16):3658-3667
Syntheses of 2,2′‐bisalcoholic group‐substituted 9,9′‐spirobifluorene monomers 2 were performed by the reaction of 2,2′‐dihydroxy‐9,9′‐spirobifluorene 2a with haloalcohols. Polycarbonates consisting of 9,9′‐spirobifluorene skeleton in the main chain (PC 4 ) were synthesized by the polycondensation of 2,2′‐bisalcoholic monomers 2 and triphosgene or diphenyl carbonate. PC 4 showed good thermal stability: the 5% weight loss temperature was over 330 °C under both nitrogen and air atmospheres. The glass transition temperature was in a range of 16–269 °C estimated by differential scanning calorimetry, depending on the flexibility of the alkylene or oxyethylene chains of 2 . PC 4 showed high solubility toward ordinary organic solvents such as CHCl3, benzene, and THF, making possible the preparation of the flexible thin films. Very high refractive index in a range of 1.62–1.66 at 589 nm was observed although PC 4 consists only of C, H, and O atoms, whereas very low degree of birefringence was confirmed. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3658–3667, 2010 相似文献
69.
Pyrene-appended alpha-cyclodextrin (3) in which a trimethylenediamine linker connected the pyrene residue to the alpha-cyclodextrin moiety showed pH-dependent fluorescence intensity changes. The fluorescence intensity was almost linearly changed within the pH range of 5 - 10. The unique fluorescence response of 3 to the pH was due not only to the favorable pK(a) values (pK(a1) = 6.4 and pK(a2) = 8.8), but also to the almost equal contributions of the amino groups to the pyrene's fluorescence quenching. 相似文献
70.
Iwao Okamoto Mayumi Nabeta Misaki Yamamoto Maiko Mikami Tetsuya Takeya Osamu Tamura 《Tetrahedron letters》2006,47(40):7143-7146
An aromatic N-methyl amide containing N-(2-pyridyl) and 2,6-pyridinedicarboxamide moieties switches its conformation from cis to trans depending upon the acceptor number of solvents. 相似文献