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51.
cis-2-Oxo-5-hydroxymethyl-1,3,2-dioxathiolane 2a can be efficiently resolved by a lipase from Pseudomonas cepacia-catalysed acylation reaction with vinylbutyrate. Compound 2a was directly prepared from glycerol in one step. This first lipase-catalysed resolution of a cyclic sulphite derivative provides a potentially useful activated chiral synthon. 相似文献
52.
A. De Giacomo M. Dell’Aglio O. De Pascale 《Applied Physics A: Materials Science & Processing》2004,79(4-6):1035-1038
In this paper the flexibility of Laser Induced Breakdown Spectroscopy (LIBS) has been proved for the analysis of water solutions. The plasma is generated directly in the bulk of a water solution by a Q-switched Nd:YAG laser (1064). The emission signal of four different solutions has been studied: AlCl3, NaCl, CaCO3 and LiF. The basic mechanisms influencing the emission signal and the experimental tricks for the optimization of the detection mode have been pointed out. PACS 52.70.Kz; 52.80.Wq; 39.30.+p 相似文献
53.
We establish a duality formula for the problem Minimize f(x)+g(x) for h(x)+k(x)<0 where g, k are extended-real-valued convex functions and f, h belong to the class of functions that can be written as the lower envelope of an arbitrary family of convex functions. Applications in d.c. and Lipschitzian optimization are given. 相似文献
54.
55.
The stochastic finite element method presented in this Note consists in representing in a probabilistic form the response of a linear mechanical system whose material properties and loading are random. Each input random variable is expanded into a Hermite polynomial series in standard normal random variables. The response (e.g., the nodal displacement vector) is expanded onto the so-called polynomial chaos. The coefficients of the expansion are obtained by a Galerkin-type method in the space of probability. To cite this article: B. Sudret et al., C. R. Mecanique 332 (2004). 相似文献
56.
To allow for a reliable examination of the interaction between velocity fluctuations, acoustics and combustion, a novel numerical procedure is discussed in which a spectral solution of the Navier–Stokes equations is directly associated to a high-order finite difference fully compressible DNS solver (sixth order PADE). Using this combination of high-order solvers with accurate boundary conditions, simulations have been performed where a turbulent premixed V-shape flame develops in grid turbulence. In the light of the DNS results, a sub-model for premixed turbulent combustion is analyzed. To cite this article: R. Hauguel et al., C. R. Mecanique 333 (2005). 相似文献
57.
A simple and practical procedure for the reduction of acetals to ethers is described. It is based on the use of a 1,1,3,3-tetramethyldisiloxane (TMDS)-Pd/C system in the presence of a Brønsted acid as the co-catalyst. The reaction occurs under mild conditions and ethers are obtained in high yields. 相似文献
58.
The synthesis of a generation 5 (G5) poly(amidoamine) (PAMAM) dendrimer platform having cyclooctyne ligands that were subsequently be used for a copper-free Huisgen 1,3-dipolar cycloaddition (click reaction) with azido modified methotrexate is described. The G5 PAMAM dendrimer was first partially (70%) acetylated and then coupled with 20 cyclooctyne ligands through amide bonds. The remaining primary amine groups on the dendrimer surface were neutralized by acetylation. The platform was then ‘clicked’ with different numbers (5, 10, and 17) of γ-azido functionalized methotrexate. The copper-free click reactions were stoichiometric with excellent yields. 相似文献
59.
The synthesis of a series of novel indazole-5,6-diamine derivatives is described. This indazole ring system was incorporated in an octahydropyrrolo[3,4-b]phenazine scaffold and was diversely and regioselectively substituted on the nitrogen atoms at the 5- and 10-positions. Thus, the nitrogen atom at the 5-position was found to be more reactive toward electrophiles than the one at the 10-position. This difference of reactivity could be attributed to the electronic effect of the pyrazole moiety. Moreover, an unexpected tetrahydropyran protecting group migration was observed from the N-1 atom to the C-11 position of the octahydropyrrolo[3,4-b]phenazine scaffold. 相似文献
60.