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51.
Brahim Lakhrissi Mohamed Massoui El Mokhtar Essassi Vincent Lequart Nicolas Joly Patrick Martin Grard Goethals 《Journal of heterocyclic chemistry》2004,41(6):1011-1014
Reaction of 1,5‐benzodiazepin‐2,4‐dione with 3‐O‐substituted‐5,6‐anhydro‐1,2‐isopropylidene‐α‐D‐glucofuranose gave the unexpected N,N'‐di‐glucofuranosyl benzimidazol‐2‐one by a novel rearrangement and ring closure reaction. A mechanism is proposed. 相似文献
52.
Peptide-based reversible and irreversible cysteine proteases inhibitors are well reported in the literature. Many of these compounds have an electrophilic carbonyl group as a cysteine trap in the place of a scissile amide moiety of the natural substrate. As a common mechanism strategy, we have designed a probe library of a cysteine trap for rapid optimization of P1-P1' pockets of different cysteine proteases. The synthesis of this library using a straightforward methodology based on polymer-supported reagents and scavengers to avoid tedious purification steps has been achieved. For the selective monobromination of diazo ketones, preparation of a new supported reagent, piperidinoaminomethylpolystyrene hydrobromide, is also described. 相似文献
53.
Patricia MerdyEmmanuel Guillon Jacques DumonceauMichel Aplincourt 《Analytica chimica acta》2002,459(1):133-142
Comparative studies using various analytical and spectroscopic techniques have been carried out on three samples of lignin: two samples of natural lignin that have been extracted using different processes, and one sample of synthetic lignin. This paper discusses the general features common to all three kinds of lignin, as well as the differences between, on one hand, the two natural lignins coming from different extraction processes, and, on the other hand, the natural lignins and the synthetic one. The advantages of each technique in explaining the structure of these three different lignins are emphasised. 相似文献
54.
M. Nicolas 《Journal of Electroanalytical Chemistry》1985,185(2):365-378
Hydrogen adsorption on plantinum polycrystalline films in methanolic medium has been studied between 293 and 163 K by cyclic voltammetry. At the same time, the electrooxidation of the solvent was followed down to the solidification point of the electrolyte. The oxidation reactions of the residues coming from methanol adsorption on platinum are thermally activated phenomena which are controlled by diffusion at very low temperature, whereas the mechanism of hydrogen adsorption does not seem to be thermally activated. The adsorption of hydrogen on Pt in methanolic medium is not all “blocked” below T = 243 K. Moreover, at low temperature, it seems to be stronger than that at room temperature. 相似文献
55.
Choua S Dutan C Cataldo L Berclaz T Geoffroy M Mézailles N Moores A Ricard L Le Floch P 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(16):4080-4090
EPR spectra show that one-electron reduction of bis(3-phenyl-6,6-(trimethylsilyl)phosphinine-2-yl)dimethylsilane (1) on an alkali mirror leads to a radical anion that is localized on a single phosphinine ring, whereas the radical anion formed from the same reaction in the presence of cryptand or from an electron transfer with sodium naphthalenide is delocalized on the two phosphinine rings. Density functional theory (DFT) calculations show that in the last species the unpaired electron is mainly confined in a loose P-P bond (3.479 A), which results from the overlap of two phosphorus p orbitals. In contrast, as attested by X-ray spectroscopy, the P-P distance in neutral 1 is large (5.8 A). As shown by crystal structure analysis, addition of a second electron leads to the formation of a classical P-P single bond (P-P 2.389 A). Spectral modifications induced by the presence of cryptand or by a change in the reaction temperature are consistent with the formation of a tight ion pair that stabilizes the radical structure localized on a single phosphinine ring. It is suggested that the structure of this pair hinders internal rotation around the C-Si bonds and prevents 1 from adopting a conformation that shortens the intramolecular P-P distance. The ability of the phosphinine radical anion to reversibly form weak P-P bonds with neutral phosphinines in the absence of steric hindrance is confirmed by EPR spectra obtained for 2,6-bis(trimethylsilyl)-3-phenylphosphinine (2). Moreover, as shown by NMR spectroscopy, in this system, which contains only one phosphinine ring, further reduction leads to an intermolecular reaction with the formation of a classical P-P bond. 相似文献
56.
P Leroy A Nicolas C Gavriloff M Matt P Netter B Bannwarth B Hercelin M Mazza 《Journal of chromatography. A》1991,564(1):258-265
A simple and fast high-performance liquid chromatographic method was developed for the simultaneous measurement of 2-mercaptopropionylglycine (Tiopronine) and its metabolite (2-mercaptopropionic acid) in human plasma after the administration of a pharmaceutical dosage form (Acadione). The sample treatment before high-performance liquid chromatographic analysis consisted of the reduction of the corresponding disulphides by tri-n-butylphosphine and protein precipitation with ethanol. Separation was achieved by ion-pair high-performance liquid chromatography on a reversed-phase column (LiChrospher RP 18e) with cetrimonium bromide as counter ion and detection by fluorimetry after post-column derivatization with a selective thiol reagent, i.e. pyrenemaleimide. The high frequency of the analyzed samples and validation results make the method suitable for pharmacokinetic studies, and this was demonstrated by the first results obtained after the administration of an oral dose of 500 mg of Tiopronine to two healthy subjects. 相似文献
57.
The Ramanujan Journal - Let $$\sigma (n)=\sum _{d\mid n}d$$ be the sum of divisors function and $$\gamma =0.577\ldots $$ the Euler constant. In 1984, Robin proved that, under the Riemann... 相似文献
58.
We consider a model of spinless fermions on a lattice, interacting through a nearest neighbor repulsion. In the half-filled band case and for dimensionsd 2, we rigorously prove that there is long-range order in some domain of the parameters=(k
B
T)–1 andt/U, wheret is the hopping amplitude of the particles,U the strength of their repulsion, and the inverse temperature. Our technique is based on the usual Peierls argument of classical statistical mechanics but fails for the groundstate. We discuss the specific difficulties introduced by the Fermi statistics.Work supported in part by U.S. NSF grant PHY 90-19433-A02. 相似文献
59.
Chevallier Nicolas 《Potential Analysis》1993,2(2):187-194
LetP be a positive contraction ofL 1, we say that a sequence (Q n ) n of positive operators is subordinated toP if $$Q_0 = Id, \forall n \in \mathbb{N} Q_n P \geqslant Q_{n + 1} .$$ Let (Q n,k ) be a double sequence of operators such that for each integerk the sequence (Q n,k ) n is subordinated toP. We prove a result of almost everywhere convergence for the quotientsW k f/W k g, whereW k f=∑ n=0 ∞ Q n,k f. 相似文献
60.