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71.
Abstract Anomeric O-alkylation of mannopyranoses with various protecting groups was investigated using mannose derivatives and 2,3-O-isopropylidene-l-O-trifluoro-methanesulfonyl-D-glycerol (1) as alkylating agent. Generally, in polar solvents higher α/β ratios were obtained than in nonpolar solvents. Sterically demanding protecting groups at the 6-O-position and polar solvents led to higher yields. Reactivity differences were explained by different complex formation. Based on these results mannopyranosyl-α(1-4) glucopyranosides 26 and 27 were synthesized using mannose derivatives 5 and 6 having a 6-O-(p-methoxyphenyl)diphenylmethyl group and galactosyl trifluoromethane-sulfonate 24 or nonafluorobutanesulfonate (nonaflate) 25, respectively, as alkylating agents. 相似文献
72.
Masahiro FujiwaraNaoya Tajima Tatsuro ImakuboMasafumi Tamura Reizo Kato 《Journal of solid state chemistry》2002,168(2):396-407
This article reports preparation, structure, and conducting property of several cation radical salts of organic donors tetramethyltetrathiafulvalene (TMTTF), ethylenedithiotetrathiafulvalene (EDT-TTF), bis(ethylenedithio)tetrathiafulvalene (ET), bis(ethylenedithio)tetraselenafulvalene (BETS) and hexamethylenetetraselenafulvalene (HMTSF) with two novel planar Te-based dianions, TeI42− and Te2I62−. (ET)5Te2I6 1 and (BETS)5Te2I6 2 are isostructural. In these Te2I62− salts, intermolecular short I···I contacts form a supramolecular corrugated anion sheet. Donor arrangement is similar to the θ-type. With lowering temperature, the resistivity of 1 shows a gradual increase followed by a sharp upturn at 110 K. 2 is metallic down to 120 K and shows a gradual increase of the resistivity followed by a clear transition to an insulating state around 60 K. Crystal structure of (ET)4TeI4 3 is based on the “herring bone” arrangement of ET molecules similar to the α-type. 3 shows a semiconductive behavior around room temperature followed by a transition to an insulating state at 210 K. (EDT-TTF)4TeI4 4, a semiconductor, exhibits a unique two-dimensional arrangement of dimerized EDT-TTF molecules. 相似文献
73.
Takagi R Miyanaga W Tamura Y Ohkata K 《Chemical communications (Cambridge, England)》2002,(18):2096-2097
The Diels-Alder reaction of spirolactones with cyclopentadiene afforded the adduct with high pi-facial selectivity; a hydrophilic analogue of scyphostatin was synthesized from the Diels-Alder adduct. 相似文献
74.
Quinolone Analogs 14: Synthesis of Antimalarial 1‐Aryl‐3‐(4‐quinolon‐2‐yl)ureas and Related Compounds 下载免费PDF全文
Yoshihisa Kurasawa Kiminari Yoshida Naoki Yamazaki Kenji Sasaki Yoshito Zamami Zhao Min Atsumi Togi Hideyuki Ito Eisuke Kaji Haruhiko Fukaya 《Journal of heterocyclic chemistry》2014,51(Z1):E241-E248
The 4‐quinolone‐2‐carbohydrazide 6a was converted into 1‐aryl‐3‐(4‐quinolon‐2‐yl)ureas 5a , 5b , 5c , 5d , 5e , 1‐aryl‐3‐(4‐quinolon‐2‐yl)imidazolidine‐2,4‐diones 9a , 9b , and N‐(4‐quinolon‐2‐yl)carbamates 10a , 10b via 4‐quinolone‐2‐carbonylazide 7a . The 4‐methoxyquinoline‐2‐carbohydrazide 6b was also transformed into 1‐aryl‐3‐(4‐methoxyquinolin‐2‐yl)ureas 11a , 11b , 11c , 11d , 1‐aryl‐3‐(4‐methoxyquinolin‐2‐yl)imidazolidine‐2,4‐diones 12a , 12b , and N‐(4‐methoxyquinolin‐2‐yl)carbamates 13a , 13b via 4‐methoxyquinoline‐2‐carbonylazide 7b . Some of the 1‐aryl‐3‐(4‐quinolon‐2‐yl)ureas 5a , 5b , 5c , 5d , 5e showed the in vitro antimalarial activity to chloroquine‐resistant Plasmodium falciparum, wherein IC50 was 0.93 to 4.00 μM. 相似文献
75.
76.
Youko Tamura Li Sheng Satoshi Nakazawa Tomoya Higashihara Mitsuru Ueda 《Journal of polymer science. Part A, Polymer chemistry》2012,50(20):4334-4340
A series of polystyrenes with phosphonic acid ( 5 ) via long alkyl side chains (4, 6, and 8 methylene units) were prepared by the radical polymerization of the corresponding diethyl ω‐(4‐vinylphenoxy)alkylphosphonates, followed by the hydrolysis with trimethylsilyl bromide. The resulting phosphonated polystyrene membranes had a high oxidative stability against Fenton's reagent at room temperature. The membranes prepared from 5 exhibited a very low water uptake, similar to that of Nafion 117 over the wide range of 30 to 80% relative humidity (RH). The proton conductivities of these membranes are lower than that of Nafion 117 in the range of 30 to 90% RH, but comparable or higher than those of the reported phosphonated polymers with higher IEC values, such as the phosphonated poly(N‐phenylacrylamide) (PDPAA, IEC: 6.72 mequiv/g) and fluorinated polymers with pendant phosphonic acids (M47, IEC: 8.5 mequiv/g), at low RH conditions despite the much lower IEC values (3.0–3.8 mequiv/g) of these membranes. These results suggest that the flexible pendant side chains of 5 would contribute to the formation of hydrogen‐bonding networks by considering the very low water uptake of these polymers. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012 相似文献
77.
Y. Leon P. Sciau P. Goudeau N. Tamura S. Webb A. Mehta 《Applied Physics A: Materials Science & Processing》2010,99(2):419-425
In addition to the red terra sigillata production, the largest Gallic workshop (La Graufesenque) made a special type of terra sigillata, called “marbled” by the archaeologists. Produced exclusively at this site, this pottery is characterized by a surface finish
made of a mixture of yellow and red slips. Because the two slips are intimately mixed, it is difficult to obtain the precise
composition of one of the two constituents without contamination from the other. In order to obtain very precise correlation
at the appropriate scale between the color aspect and the elemental and mineralogical phase distributions in the slip, combined
electron microprobe, X-ray micro spectroscopies and micro diffraction on cross-sectional samples were performed. The aim of
this study is to discover how potters were able to produce this unique type of terra sigillata and especially this particular slip of an intense yellow color. Results show that the yellow component of marbled sigillata was made from a titanium-rich clay preparation. The color is due to the formation of a pseudobrookite (TiFe2O5) phase in the yellow part of the slip, the main characteristics of that structure being considered nowadays as essential
for the fabrication of stable yellow ceramic pigments. Its physical properties such as high refractive indices and a melting
point higher than that of most silicates widely used as ceramic colorants are indeed determinant for this kind of application.
Finally, the red parts have a similar composition (elementary and mineralogical) to the one of standard red slip. 相似文献
78.
Akagi M Omae D Tamura Y Ueda T Kumashiro T Urata H 《Chemical & pharmaceutical bulletin》2002,50(6):866-868
L-Ribose was synthesized by a simple four-step method with overall yield of 76.3% from a protected L-arabinose derivative, which is a compatible intermediate for the synthesis of L-deoxyribose. The key step of this strategy is the Swern oxidation and subsequent stereoselective reduction accompanied by inversion of the 2-hydroxy group of protected L-arabinose. 相似文献
79.
Toriya S Tamura Y Takei T Fuji M Watanabe T Chikazawa M 《Journal of colloid and interface science》2002,255(1):171-176
The silica-pillared derivatives from kanemite (NaHSi(2)O(5).3H(2)O) were prepared by intercalation of dialkyldimethylammonium (DADMA) ion and pillaring with tetraethylorthosilicate. The formation of silica pillars between the silicate sheets was demonstrated by X-ray diffraction, (29)Si CP/MAS NMR, and TEM observation. The basal spacing depended on the chain length of DADMA. Nitrogen adsorption study showed that the specific surface area was enlarged over 1000 m(2) g(-1) by the pillaring and that the pore size was in the micropore region. Water and benzene adsorption isotherms revealed that the surface properties of the pillared derivatives show hydrophobic character. 相似文献
80.
Treatment of O-tert-butyldimethylsilyloximes having olefin moieties in the molecules with BF3.OEt2 results in efficient generation of N-borano-nitrones, which undergo intramolecular cycloaddition at room temperature to afford N-nonsubstituted cycloadducts after work-up. 相似文献