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261.
在α次积分半群的扰动理论的基础上,讨论了α次积分C-半群的可交换扰动问题,得到了α次积分D半群的扰动定理. 相似文献
262.
《Analytical letters》2012,45(14):1185-1189
Abstract A specific and non-destructive test for basic esters of benzilic and α-glycolic acids in water is described. The compounds are collected on a glass fiber filter as water insoluble complexes with sodium tetraphenylboron. The filter is dried and sprayed with a 2-diphenylacetyl-l, 3-indandione-l-imine derivative. A positive test is the visual observation of fluorescence. 相似文献
263.
Alexandre Lumbroso Isabelle Beaudet Thierry Besson Erwan Le Grognec 《Tetrahedron》2009,65(45):9180-45
An efficient and reproducible synthesis of various α-ethoxycarbamates is described via a microwave heating mode. Compared to the thermal process, the microwave dielectric heating induces a dramatic reduction of the reaction time and the improvement of the yields. The reaction is general since applicable to aromatic and aliphatic aldehydes with various primary amines. Several examples involving chiral aldehydes have also been considered. 相似文献
264.
《Green Chemistry Letters and Reviews》2013,6(3):205-208
Abstract An efficient and convenient procedure for the synthesis of thiazole derivatives from α-haloketone, thiourea and substituted acetophenones using polyethylene glycol-400 as a green and recyclable solvent is described. Significant rate enhancement and improved yields have been observed. 相似文献
265.
《Green Chemistry Letters and Reviews》2013,6(3):213-216
Abstract A simple, efficient, and practical procedure for the synthesis of various substituted 2,3-dihydro-2-phenyl-1H-naphtho[1,2-e][1,3]oxazines and 3,4-dihydro-3-phenyl-2H-naphtho[2,1-e][1,3]oxazines using KAl(SO4)2 12H2O (alum) as a non-toxic, reusable, inexpensive, and easily available catalyst is described using water as a solvent. These improved reaction conditions allow the preparation of a wide variety of substituted [1,3]oxazines in high yields and purity under mild reaction conditions. 相似文献
266.
Maria Carmelita Z. Kasuya Maki Ikeda Kazuhiko Hashimoto Toshinori Sato 《Journal of carbohydrate chemistry》2013,32(7):705-715
The synthesis of sialylated glycosides using saccharide primers and cells was investigated. α · and β · Saccharide primers were chemically synthesized and introduced into B16 melanoma cells to prime oligosaccharide synthesis. Incorporation of α‐ and β‐dodecyl lactosides into B16 cells resulted in the sialylation of the galactose residue to give GM3‐type oligosaccharides. The β‐dodecyl galactoside primer was sialylated but the α‐dodecyl galactoside primer was not. Both the α‐ and β‐dodecyl glucoside primers were not elongated. In the glycosylation of primers by cells, this research confirmed that sialyl transferases tolerate acceptor modifications and are permissive to primer elongation regardless of the α‐ or β‐linkage to the aglycon unit. However, the presence of the terminal galactose residue that is β‐linked to the adjacent saccharide or aglycon unit is essential for sialylation by cellular enzymes to occur. 相似文献
267.
Renaud Beaudegnies Alain De Mesmaeker Aurélie Mallinger Myriam Baalouch André Goetz 《Tetrahedron letters》2010,51(20):2741-3222
We report the design and the efficient synthesis of novel spirocyclopropyl cyclohexane-1,3-dione and -1,3,5-trione units to be incorporated into potent HPPD inhibitors. New routes involving original combinations of synthetic equivalents of α-cyclopropyl ketone-α-anion and α-cyclopropyl ester-β-cation are described. 相似文献
268.
V. Bernabé-Zafón M. Beneito-CambraE.F. Simó-Alfonso J.M. Herrero-Martínez 《Journal of chromatography. A》2010,1217(19):3231-3237
The synthesis of lauryl methacrylate monoliths for capillary electrochromatography by UV polymerization using several free-radical initiators (α,α′-azobisisobutyronitrile, 2,2-dimethoxy-2-phenylacetophenone, dibenzoyl peroxide (BPO) and lauroyl peroxide (LPO)) has been investigated. Using a 1,4-butanediol/1-propanol mixture as porogenic solvent, the influence of each initiator and its content on the morphological and electrochromatographical properties of beds was evaluated. Under their respective optimum content, satisfactory separations of a test mixture of PAHs with similar efficiencies (minimum plate heights of 8.0–12.7 μm obtained from Van Deemter plots) were achieved for the four investigated photo-initiators. The columns photo-polymerized with LPO provided the best compromise between chromatographic performance and analysis time. Moreover, this initiator showed a fine control in the column retention properties. The resulting monolithic columns exhibited a good run-to-run repeatability in the tested chromatographic parameters (RSD < 2.4%) for all initiators investigated; and satisfactory column-to-column repeatability (RSD < 6.0%), except for beds photo-polymerized with BPO (RSD < 10.8%). 相似文献
269.
α-Actinin has been shown to be capable of interacting with some special membrane phospholipids directly, which is important for its function. In this study, hybrid bilayer membranes composed of negatively charged lipids are constructed on the surface plasmon resonance gold substrate and on the gold electrode, respectively, and the interaction between α-actinin and negatively charged lipids membrane is investigated by surface plasmon resonance, cyclic voltammetry and electrochemical impedance spectroscopy methods. α-Actinin is proved to be able to interact with the negatively charged lipids membrane directly. It can also insert at least partly into the membrane or lead to some defect or lesion in the membrane, which increase the permeability of the membrane. This study would bring some insight on the interaction between the α-actinin and the cell membranes in vivo. 相似文献
270.
The behavior of (ferrocene)amylose (FA), in the presence of amylolytic depolymerases (α-amylase from Aspergillus oryzae and human saliva), has been investigated by cyclic voltammetry at a rotating disk electrode (CVA/RDE). Growth of the limiting current with time in the presence of the enzymes is proportional to the amount of enzyme introduced. The quantitative data treatment to assay the endoamylolytic activity of enzymes at CVA/RDE involves plotting (idt/id0)4.5 against time; the slope of the linear plot being equal to (rate) Mn0C−1, where idt and id0 are the limiting currents at time t and 0, respectively, (rate) is the enzymatic activity, Mn0 is the number averaged molecular weight of FA at t = 0, and c is its concentration. The comparison of CVA/RDE with the 3,5-dinitrosalicylic acid and the Somogyi–Nelson reducing saccharides procedures shows advantages of the former, especially in assaying small quantities of enzymes. Also the CVA/RDE approach is simpler and takes place under much milder conditions. The main disadvantage of CVA/RDE is the inhibiting effect of Triton X-100 in the reaction between FA and the amylases which is not observed in the case of native, ferrocene-free amylose. In general, CVA/RDE appears to be an attractive analytical method for monitoring diverse enzymatic depolymerization reactions. 相似文献