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排序方式: 共有133条查询结果,搜索用时 15 毫秒
131.
Tokuyuki Kuroda Koji Hisamura Ikuo Matsukuma Yutaka Osawa Toru Sugaya Hiroshi Nishikawa Makoto Morimoto Tadashi Ashizawa Nobuhiro Nakamizo Yoshio Otsuji 《Journal of heterocyclic chemistry》1994,31(1):113-119
A variety of mitomycin C analogs were synthesized from mitomycin A and their biological activities were studied. Mitomycin A ( 1 ) underwent nucleophilic displacement reactions involving intramolecular hydrogen migrations upon treatment with nitrogen nucleophiles bearing mobile hydrogens, but the mode of hydrogen migration depended on the nature of the nucleophiles. The reaction with alkoxyamines gave compounds 6 and 7 which have the 5H-6-alkoxyimino-4,7-dione structure in ring A of 1 . However, the reaction with hydroxylamine and benzoylhydrazine afforded compounds 11 and 13 which have the 4-hydroxy-6-hydroxyimino-7-one structure and the 4-hydroxy-6-hydrazono-7-one structure, respectively, in ring A of 1 . These products were converted into various types of mitomycin C derivatives by methylation with methyl iodide or dimethyl sulfate. The mechanistic features of these reactions are discussed. The in vitro and in vivo biological activities were tested by using P388 leukemia and Sarcoma 180 tumor cells. Several of the synthesized compounds exhibited better activity than that of mitomycin C. 相似文献
132.
Takuya Mabe Fumiaki Doseki Takeyoshi Yagyu Koji Ishihara Masahiko Inamo Hideo D. Takagi 《Journal of solution chemistry》2018,47(6):993-1020
The second-order electron transfer reaction between the photo-excited triplet state of [Zn(TPP)]* (TPP?=?5,10,15,20-tetraphenylporphyrin) and [Co(sep)]3+ (sep?=?sepulchrate?=?1,3,6,8,10,13,16,19-octaazabicyclo[6.6.6]eicosane) was investigated in three ionic liquids (ILs, 1-R-3-methylimidazolium bis(trifluoromethylsulfonyl)imide with R?=?butyl, pentyl, and hexyl) and in acetonitrile. Results of electrochemical and kinetic measurements indicated that ILs dissociate in the vicinity of charged metal complexes and at electrodes, although the dissociated anionic and cationic components of the ILs seem to exist as pairs around the metal complexes. Second-order rate constants for the electron transfer reaction are 1.88?×?109, 3.65?×?107, 2.63?×?107, and 2.01?×?107 kg·mol?1·s?1 in acetonitrile and in the butyl, pentyl and hexyl ILs, respectively, at 298 K, after correction of the contribution of diffusion. The average slope of the plot of the logarithmic second-order rate constants observed in acetonitrile and ILs against the logarithmic viscosity of each solvent was ??0.84. However, the slope of the same plot was much steeper (??4.1) when data for only the three ILs were used. Detailed analyses of the experimental results on the basis of the Latner–Levin cross relation and the Marcus theory lead to the conclusion that the solvent properties such as the dielectric constant and refractive index around the polarized/charged transition states are different from those for the bulk ILs: observed self-exchange rate constants did not exhibit the Pekar factor dependence when dielectric constants and refractive indices for bulk ILs are used. 相似文献
133.
Ahmed I. Abdelrahman Ahmad M. Mohammad Mohamed S. El-Deab Takeyoshi Okajima Takeo Ohsaka 《Macromolecular Symposia》2008,270(1):74-81
The layer-by-layer (LBL) approach has been utilized to self-assemble multilayers films of citrate-stabilized gold nanoparticles (AuNPs) on polycrystalline gold (poly-Au) substrates. 1,4-benzenedimethanethiol (BDMT) was used as a cross linker to bind every two successive AuNPs layers. The transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) techniques were employed to confirm the existence of the alternative layers of AuNPs and BDMT in the self-assembled multilayers film. The AuNPs modified poly-Au electrode showed a significant electrocatalysis towards the reduction of oxygen (a positive potential shift of about 100 mV was observed in the reduction peak potential compared to that obtained at the bare poly-Au electrode). The AuNPs tend to aggregate during their assembling to different extent which markedly depends on the substrate geometry and roughness. An effort was dedicated to understand and control the aggregation phenomenon. 相似文献