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51.
W. Clark Still Lawrence J. Macpherson Toshiro Harada James F. Callahan Arnold L. Rheingold 《Tetrahedron》1984,40(12):2275-2281
The conformations of macrocyclic intermediates provide a useful medium through which distant chiral centers may control chemical reactions. In this paper, we show that macrocycles made by cyclization of simple acyclic starting materials with an auxiliary spacer may be used to prepare stereochemically complex acyclic products. 相似文献
52.
Concanavalin A (Con A) was biotinylated to various degrees using N-biotinyl-omega-aminocaproic-acid-N-hydroxy succinimide ester as the biotinylation reagent, and then analyzed by isoelectric focusing using PhastGel IEF 3-9. The isoelectric points of biotinylated ConAs were found to decrease with increasing concentration of the biotinylation reagent. Analysis by isoelectric focusing followed by dot blotting clearly indicated that the biotinylated ConA with an isoelectric point lower than that of the original ConA by 2.2 +/- 0.6 had the strongest binding activity for ovalbumin. 相似文献
53.
Tamás Veszprémi Yoshiya Harada Koichi Ohno Hideki Mutoh 《Journal of organometallic chemistry》1983,252(2):121-125
Penning ionization electron spectroscopy and CNDO/S calculations have been successfully applied to the analyses of the UV photoelectron spectra of 2- and 2,5-bistrimethylsilylthiophene and 2-t-butylthiophene. The relative intensities of the π type bands are greatly enhanced in the Penning spectra compared with those of the UV photoelectron spectra. 相似文献
54.
Ichimin Shirotani Yousuke Shimaya Chihiro Sekine 《Journal of solid state chemistry》2003,174(1):32-34
New filled skutterudites with heavy lanthanide, LnFe4P12 (Ln=Tb, Dy, Ho, Er, Tm, Yb, Lu and Y) have systematically been prepared for the first time by the high-pressure technique. The relationship between lattice constants and atomic numbers of lanthanide (including Y) is established for LnFe4P12. Electrical and magnetic properties of several new filled skutterudites with heavy lanthanide have been studied at low temperatures; YFe4P12 shows a superconducting transition at around 7 K, and DyFe4P12 behaves as a ferromagnet below 10 K. Electrical and magnetic anomalies in DyFe4P12 and YFe4P12 are mainly discussed. 相似文献
55.
Choji Kashima Shigeki Hibi Tatsuya Maruyama Kazuo Harada Yoshimori Omote 《Journal of heterocyclic chemistry》1987,24(3):637-639
The relative reaction rate of five-membered heterocycles with ozone was evaluated. These relative rates were correlated to the highest bond order value in the corresponding ring, calculated by the convenient HMO method. From this correlation, the reactivity of heterocycles with ozone was able to be predicted. Also it was concluded that the predominant product in the ozonolysis of five-membered heterocycles containing an oxygen atom was the corresponding carboxylic acid, while nitrogen heterocycles gave the corresponding amide. 相似文献
56.
Tetsuro Kato Ryosuke Nemoto Hisashi Mori Ryoetsu Abe Katsuo Unno Akio Goto Hideyuki Murota Masaoki Harada Motofumi Homma 《Applied biochemistry and biotechnology》1984,10(1-3):199-211
To achieve targeted distribution of anticancer drugs with sustained activity, ferromagnetic ethylcellulose microcapsules containing
an anticancer drug, mitomycin C (FM-MMC-mc), were prepared by a method based on phase separation principles. Two prototypes
of FM-MMC-mc were made: one with the drug as the core and zinc ferrite on its capsular surface (outer type); the other with
both the drug and zinc ferrite as the core (inner type). Both preparations provided a sustained-release property and a sensitive
response to conventional magnetic force, although certain differences in the release rate of drug, magnetic responsiveness,
and particle size were found between the two dosage forms. Animal studies showed that the magnetic microcapsules could be
magnetically controlled in the artery and urinary bladder. VX2 tumors in the rabbit hind limb and urinary bladder were successfully
treated with magnetic control of FM-MMC-mc. Pharmacokinetic study revealed that the targeting of the microcapsules markedly
enhanced the drug absorption into the surrounding tissues for a prolonged period of time. The results indicate the feasibility
and effectiveness of the magnetic microcapsules as a targeted drug delivery system. 相似文献
57.
Satoshi Takamizawa Dr. Chihiro Kachi‐Terajima Dr. Masa‐aki Kohbara Takamasa Akatsuka Tetsuro Jin Dr. 《化学:亚洲杂志》2007,2(7):837-848
The vapor absorbency of the series of alcohols methanol, ethanol, 1‐propanol, 1‐butanol, and 1‐pentanol was characterized on the single‐crystal adsorbents [MII2(bza)4(pyz)]n (bza=benzoate, pyz=pyrazine, M=Rh ( 1 ), Cu ( 2 )). The crystal structures of all the alcohol inclusions were determined by single‐crystal X‐ray crystallography at 90 K. The crystal‐phase transition induced by guest adsorption occurred in the inclusion crystals except for 1‐propanol. A hydrogen‐bonded dimer of adsorbed alcohol was found in the methanol‐ and ethanol‐inclusion crystals, which is similar to a previous observation in 2 ?2EtOH (S. Takamizawa, T. Saito, T. Akatsuka, E. Nakata, Inorg. Chem. 2005 , 44, 1421–1424). In contrast, an isolated monomer was present in the channel for 1‐propanol, 1‐butanol, and 1‐pentanol inclusions. All adsorbed alcohols were stabilized by hydrophilic and/or hydrophobic interactions between host and guest. From the combined results of microscopic determination (crystal structure) and macroscopic observation (gas‐adsorption property), the observed transition induced by gas adsorption is explained by stepwise inclusion into the individual cavities, which is called the “step‐loading effect.” Alcohol/water separation was attempted by a pervaporation technique with microcrystals of 2 dispersed in a poly(dimethylsiloxane) membrane. In the alcohol/water separation, the membrane showed effective separation ability and gave separation factors (alcohol/water) of 5.6 and 4.7 for methanol and ethanol at room temperature, respectively. 相似文献
58.
[reaction: see text] The enantioselective total syntheses of (+)-azimine and (+)-carpaine have been developed, starting with (S)-1,2,4-butanetriol as a single source of chirality. The key common feature in these syntheses involves stereoselective intramolecular hetero-Diels-Alder reaction of an acylnitroso compound. The critical macrocyclic dilactonization of the N-Cbz derivatives of azimic acid and carpamic acid was efficiently achieved by using the Yamguchi macrocyclization conditions. 相似文献
59.
Harada H Kazami J Watanuki S Tsuzuki R Sudoh K Fujimori A Tanaka A Tsukamoto S Yanagisawa I 《Chemical & pharmaceutical bulletin》2001,49(5):606-612
In the present article we wish to report the discovery of a novel class of ET(A)-selective endothelin (ET) receptor antagonists through the modification of the ET(A)/ET(B) non-selective antagonist, Ro47-0203 (Bosentan, 1). Replacement of the benzenesulfonamide group of 1 with a 2-phenylethenesulfonamide group gave compound 5a and resulted in improvement in ET(A)-selectivity. Optimization of the alkoxy side chain attached to the core pyrimidine ring yielded the 2-fluoroethoxy derivative (5n) with further improvement of ET(A)-selectivity. [IC50=2.1 nM for ET(A) receptor, ET(B)/ET(A) ratio=1200]. After oral administration, compound 5n inhibited the big ET-1 induced pressor response in pithed rats with a DR2 value of 2.6 mg/kg and also exhibited a potent antagonistic activity in conscious rats. 相似文献
60.
Kubo M Takizawa T Wakai C Matubayasi N Nakahara M 《The Journal of chemical physics》2004,121(2):960-969
The site-selective H/D exchange reaction of phenol in sub- and supercritical water is studied without added catalysts. In subcritical water in equilibrium with steam at 210-240 degrees C, the H/D exchange proceeds both at the ortho and para sites in the phenyl ring, with no exchange observed at the meta site. The pseudo-first-order rate constants are of the order of 10(-4) s(-1); 50% larger for the ortho than for the para site. In supercritical water, the exchange is observed also at the meta site with the rate constant in the range of 10(-6)-10(-4) s(-1). As the bulk density decreases, the exchange slows down and the site selectivity toward the ortho is enhanced. The enhancement is due to the phenol-water interaction preference at the atomic resolution. The site selectivity toward the ortho is further enhanced when the reaction is carried out in benzene/water solution. Using such selectivity control and the reversible nature of the hydrothermal deuteration/protonation process, it is feasible to synthesize phenyl compounds that are deuterated at any topological combination of ortho, meta, and para sites. 相似文献