Schizophyllans carrying oligosaccharide appendages as potential candidates for cell-targeted antisense carrier

Schizophyllans carrying beta-lactoside and alpha-mannoside appendages were prepared from native schizophyllan through NaIO4 oxidation followed by reductive amination using aminoethyl-beta-lactoside and alpha-mannoside, respectively. The resulting schizophyllans form stable macromolecular complexes with polynucleotides, such as poly(C) and poly(dA). Specific affinity between these macromolecular complexes and saccharide-binding proteins was demonstrated by surface plasmon resonance and agarose gel staining assays. beta-lactoside-appended schizophyllan enhanced an antisense activity in hepatocytes which express lactoside-binding proteins on their cell surfaces.     

Oxidation of 3-hydroxypiperidines with iodosylbenzene in water: tandem oxidative Grob fragmentation-cyclization reaction

Oxidation of 3-hydroxypiperidine with iodosylbenzene in water afforded 2-pyrrolidinone directly in good yields. The reaction probably involves oxidative Grob fragmentation yielding imino aldehyde, which upon hydrolysis produces 2-pyrrolidinone via a cyclization-oxidation sequence.     

Linear programming with multiple choice constraints for single chain undiscounted Markov decision problems

This paper develops an efficient LP algorithm for solving single chain undiscounted Markov decision problems. The algorithm imposes, in the framework of the simplex method, the multiple choice constraints that exactly one basic variable be chosen from each Markov state. It is proved that the algorithm converges to an optimal solution in a finite number of steps.     

Double tracer autoradiography of bone tumor using 3H-thymidine and radionuclides for diagnostic purpose

Whole body distribution and accumulation of radionuclide for diagnostic purpose such as 99mTc-MDP (methylene diphosphonate), 67Ga-citrate (67Ga) and 201Tl-chloride (201Tl) in implanted osteosarcoma of human origin were evaluated by macroautoradiography of Balb/c nude mouse. 3H-thymidine of which uptake has a close relation to growth pattern of tumors was used for a partner of target nuclide in double tracer technique to examine the distribution characteristics. Separated distribution pattern of coupled nuclides was imaged by a difference both of half life and energy of radiation between radionuclides. The distribution pattern of each target nuclide and 3H-thymidine were compared to clarify distribution characteristics respectively in specimen. 67Ga and 201Tl were taken around the tumor and the mode of their distribution was identical to that of 3H-thymidine. Uptake of 67Ga in tumor was much higher. 99mTc-MDP accumulated in the central zone of the tumor and its pattern was quite different from that of 3H-thymidine. From above result it was demonstrated that the accumulation mechanism of 67Ga, 201Tl and 99mTc-MDP are quite different in the tumor each other. So we concluded that our method of double tracer technique was useful for evaluation of distribution pattern of radionuclides for diagnostic purpose.     

Living radical polymerizations with germanium, tin, and phosphorus catalysts--reversible chain transfer catalyzed polymerizations (RTCPs)

A novel class of living radical polymerizations with germanium, tin, and phosphorus catalysts were developed. The polymerizations are based on a new reversible activation mechanism, Reversible chain Transfer (RT) catalysis. Low-polydispersity (M(w)/M(n) approximately 1.1-1.3) polystyrene, poly(methyl methacrylate), poly(glycidyl methacrylate), and poly(2-hydroxyethyl methacrylate) with predicted molecular weight were obtained with fairly high conversion in a fairly short time. The pseudo-first-order activation rate constant kact for the styrene/GeI4 (catalyst) system was large enough, even with a small amount of GeI4, explaining why the system provides low-polydispersity polymers from an early stage of polymerization. The retardation in the polymerization rate observed for the styrene/GeI4 system was kinetically proven to be mainly due to the cross-termination between the propagating radical with GeI3*. Attractive features of the germanium, tin, and phosphorus catalysts include their high reactivity hence small amounts (1-10 mM) being required under relatively mild conditions (at 60-100 degrees C), high solubility in organic media without ligands, insensitivity to air hence sample preparation being allowed in the air, and minor color and smell. The germanium and phosphorus catalysts may also be attractive for their low toxicity. The phosphorus catalysts may also be attractive for their low cost.     

Chromonic/Silica nanohybrids: synthesis and macroscopic alignment

Some dye molecules self-aggregate to exhibit a lyotropic columnar liquid crystal state (chromonic liquid crystal) via pi stacking in relatively highly concentrated aqueous solutions. In this work, the chromonic liquid crystal structure was immobilized, for the first time, with silica networks by way of the sol-gel condensation process. The immobilization of the columnar structure was successfully attained in the presence of 2-(2-aminoethoxy)ethanol, which favorably mediates the interface between the anionic charge of the dye aggregates and the silica network. Without this molecule, the sol-gel process gave rise to a transformation from columnar to lamellar structure. Both spin-coating and dip-coating methods gave essentially the same results. In the dip-coated films, the dye molecules were aligned over a large area with orientation orthogonal to the lifting direction.     

Coordination chemistry of a kinetically stabilized germabenzene: syntheses and properties of stable eta6-germabenzene complexes coordinated to transition metals

The first stable eta6-germabenzene complexes, that is, [M(CO)3(eta6-C5H5GeTbt)] {M=Cr (2), Mo (3), and W (4); Tbt=2,4,6-tris[bis(trimethylsilyl)methyl]phenyl}, have been synthesized by ligand-exchange reactions between [M(CO)3(CH3CN)3] (M=Cr, Mo, and W) and the kinetically stabilized germabenzene 1 and characterized by 1H and 13C NMR, IR, and UV/Vis spectroscopy. In the 1H and 13C NMR spectra of 2-4, all of the signals for the germabenzene rings were shifted upfield relative to their counterparts in the free germabenzene 1. X-ray crystallographic analysis of 2 and 4 revealed that the germabenzene ligand was nearly planar and was coordinated to the M(CO)3 group (M=Cr, W) in an eta6 fashion. The formation of complexes 2-4 from germabenzene 1 should be noted as the application of germaaromatics as 6pi-electron ligands toward complexation with Group 6 metals. On the other hand, treatment of 1 with [{RuCp*Cl}4] (Cp*=C5Me5) in THF afforded a novel eta5-germacyclohexadienido complex of ruthenium-[RuCp*{eta5-C5H5GeTbt(Cl)}] (9)-instead of the expected eta6-germabenzene-ruthenium cationic complex [RuCp*{eta6-C5H5GeTbt}]Cl (10). Crystallographic structural analysis of 9 showed that the five carbon atoms of the germacyclohexadienido ligand of 9 were coordinated to the Ru center in an eta5 fashion.     

Copper-mediated intermolecular direct biaryl coupling

Copper-mediated intermolecular direct biaryl coupling of arylazines and azoles via dual C-H bond cleavage proceeds even without palladium catalysts. The reaction system shows the high potential of copper salts in direct C-H arylation chemistry and provides a new approach to biaryl motifs, which are ubiquitous in pharmaceuticals and functional materials.     

Lasing of middle-infrared free-election lasers using the storage ring NIJI-IV

We report for the first time to our knowledge the experimental realization of a storage ring free-electron laser (FEL) in the middle-infrared (MIR) region. A technique to adjust the optical cavity using higher harmonic FELs was developed for a fundamental FEL in the MIR region. The MIR FELs were oscillated in the wavelength region of 2475 to 2673 nm, and the relative linewidth was 5×10??. A quasi-monochromatic x-ray beam with an energy of 700 keV was generated using FEL Compton backscattering. We were able to realize a quasi-monochromatic x-ray beam, whose energy is difficult to generate even in advanced synchrotron radiation facilities.