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21.
[formula: see text] The generation of (2-PyMe2Si)2CHLi was easily accomplished by the deprotonation of (2-PyMe2Si)2CH2 using n-BuLi in Et2O. Thus generated (2-PyMe2Si)2CHLi was found to react with a variety of aldehydes and ketones to give the corresponding vinylsilanes in extremely high yields with complete stereoselectivities. 相似文献
22.
An attempt to estimate the thermal decomposition mechanism of polymers using the simultaneous TG-DTA/FT-IR system was summarized. The library search of FT-IR spectra at various temperatures and of the subtraction spectrum obtained by subtracting the spectra at different temperatures were used to determine the types of evolved gases from poly(ethylene terephthalate) and poly(butylene terephthalate) at given stages of decomposition. The quantitative analysis of evolved gases was carried out using the specific gas profiles at the specific absorption band. The kinetic parameters were estimated from both TG and spectroscopic curves measured at various heating rates. 相似文献
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H. Yoshida 《Israel Journal of Mathematics》1986,54(3):366-380
Given two kinds of functionsf(X) andh(y) defined on them-dimensional Euclidean spaceR m (m≧1) and the set of positive real numbers respectively, we give an estimation of growth of subharmonic functionsu(P) defined onR m+n (n≧1) such that $$u(P) \leqq f\left( X \right)h\left( {\left\| Y \right\|} \right)$$ for anyP=(X, Y),X ∈R m, Y ∈R n, where ‖Y ‖ denotes the usual norm ofY. Using an obtained result, we give a sharpened form of an ordinary Phragmén-Lindelöf theorem with respect to the generalized cylinderD ×R n, with a bounded domainD inR m. 相似文献
25.
Flameless atomic absorption spectrometry (flameless a.a.s.) was applied to study the state of mercury deposited on a gold plate electrode from very dilute mercury(II) solution by controlled-potential electrolysis. A stable monolayer is formed on the gold electrode by the electrolysis at a potential about 200 mV more positive than the reversible Nernst potential for the reduction of mercury(II) to mercury(0). After the monolayer formation, bulk mercury is deposited on the monolayer at the reversible potential and an adatom layer is also found. The difference of activation free energies between the evaporation of mercury from the monolayer and that from bulk mercury corresponds to the underpotential shift for the electrodeposition of mercury on the gold electrode. 相似文献
26.
Very recently, we[1] found that L-proline amides and dipeptides acted as efficient catalysts for the asymmetric direct aldol reaction. We report here that L-proline-based peptides 1~5 can catalyze the aldol reactions of hydroxyacetone with aldehydes 6 in aqueous media, to give 1,4-diols (7), the disfavored products with either aldolase or L-proline. Both peptides 3 and 4 give good results. 相似文献
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Structure-activity relationships of a new antifungal imidazole, AFK-108, and related compounds 总被引:1,自引:0,他引:1
Hori K Sakaguchi A Kudoh M Ishida K Aoyama Y Yoshida Y 《Chemical & pharmaceutical bulletin》2000,48(1):60-64
Fungicidal activity of widely used imidazole antifungal drugs in topical applications is not so strong in spite of their fungistatic activities against dermatophytes and pathogenic yeasts. In order to improve fungicidal activity of imidazole antifungal agents, a series of novel imidazole derivatives having a hydrophobic substituent derived from isoprenoid were synthesized. The efficacy of these compounds was evaluated with respect to direct cell-membrane damaging activity, ergosterol biosynthesis inhibition, minimum growth-inhibitory concentration (MIC) and therapeutic effect for experimental dermatophytosis of guinea pigs. Among the newly synthesized compounds, the geranyl derivative named AFK-108 (2a) showed the highest in vivo fungicidal activity with both cell membrane damaging activity and ergosterol biosynthesis inhibition in vitro. 相似文献
29.
Chesney A Bryce MR Yoshida S Perepichka IF 《Chemistry (Weinheim an der Bergstrasse, Germany)》2000,6(7):1153-1159
Two conceptually different routes to transient 1,2-diselones are reported: 1) via ring fragmentation of the 1,4,2-diselenazine system 6, and 2) by the tributylphosphane-induced depolymerisation of the shelf-stable organoselenium polymer 15. Evidence for the intermediacy of 1,2-diselone species 7 and 16 is provided in both cases by in situ trapping with dimethyl acetylenedicarboxylate (DMAD) to yield 1,4-diselenin derivatives. The route via 15 is especially expedient and trapping of 16 is efficient. Subsequent reactions of adduct 17 afford [1,2-ethanediylbis(diphenylphosphane)] [5,6-bis(methoxycarbonyl)-1,4-diselenin-2,3-dithiolato]nickel(IV) (20). Theoretical calculations at Hartree-Fock (HF) and Moller-Plesset electron-correlated levels (MP2) suggest that the cyclic 1,2-diselenete structure 7c is significantly more stable than the acyclic 1,2-diselone structure 7a. For the bicyclic system 16, the difference in energy between the cyclic and acyclic structures is considerably reduced due to the conformational rigidity imposed by the fused 1,3-dithiole ring. In contrast, the acyclic structures of the 1,2-dithione analogues 13a and 25a are computed to be more stable than their corresponding cyclic 1,2-dithiete structures 13c and 25c. 相似文献
30.