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41.
Kittaka A Kurihara M Peleg S Suhara Y Takayama H 《Chemical & pharmaceutical bulletin》2003,51(3):357-358
Hereditary vitamin D-resistant rickets (HVDRR) is a genetic disorder caused by mutations in the vitamin D receptor, which lead to resistance to 1alpha,25-dihydroxyvitamin D(3) [1alpha,25(OH)(2)D(3)]. We found that the A ring-modified analogues, 2alpha-(3-hydroxypropyl)- and 2alpha-(3-hydroxypropoxy)-1alpha,25(OH)(2)D(3), (O1C3 and O2C3) can bind better than the natural hormone to the mutant VDR (R274A), which similar to the HVDRR mutant, R274L, had lost the hydrogen bond to the 1alpha-hydroxyl group of 1alpha,25(OH)(2)D(3). 相似文献
42.
Barbier-type Zn and In-mediated allylations of an N,N-(dimethylsulfamoyl)-protected aldimine with different allyl bromides were investigated for the preparation of N-homoallylic sulfamides. The desired N,N-(dimethylsulfamoyl)-protected products were obtained in moderate to high yields in THF as the optimal solvent. Their further derivatization was demonstrated by a facile preparation of a functionalized dehydropiperidine by an allylation/olefin metathesis reaction sequence. A high yielding deprotection of the N,N-dimethylsulfamoyl group was likewise demonstrated. 相似文献
43.
Muñoz-Hernández MA Montiel-Palma V Huitrón-Rattinger E Cortés-Llamas S Tiempos-Flores N Grevy JM Silvestru C Power P 《Dalton transactions (Cambridge, England : 2003)》2005,(1):193-199
Dichloro and chloromethyl Ga(III) complexes of general formulae [XClGa-eta2-{R2P(E)NP(E'R'2-E,E'}](X = Cl, R, R'= Ph, E, E'= O (1), S (2), Se (3); R = Ph, R'= OEt, E = O, E'= S (4); R = Me, R'= Ph, E, E'= S (5) and X = Me, E, E'= O (6), S (7), Se (8)) were synthesised by either metathesis reactions between GaCl3 and the potassium salt of the ligand (X = Cl) or by methane eliminations from in situ prepared GaMe2Cl and the protonated ligands LH (X = Me). Redistribution reaction of (3) in either CDCl3 or THF afforded the solvent-free tetracoordinate gallium spirocycle cation [Ga-{eta2-{Ph2P(Se)NP(Se)Ph2-Se,Se'})2]+ (9+). The molecular structures of complexes 2, 4, 5, 7 and 9(+) show non-planar gallacycle rings. 相似文献
44.
Cozzolino S Galantini L Leggio C Pavel NV 《The journal of physical chemistry. B》2005,109(13):6111-6120
Small-Angle X-ray Scattering (SAXS) and Dynamic Light Scattering (DLS) measurements were carried out on aqueous micellar solutions of the ionic biological detergent sodium taurodeoxycholate (NaTDC). Apparent diffusion coefficients (D(app)) and SAXS spectra of NaTDC 0.1 M solutions at different ionic strengths (0.1-0.3 M NaCl) were reported. A comparative analysis of SAXS spectra and D(app) data was performed to infer information on particle structure and interaction potential. Uniform particles with a spherical, an oblate, and a prolate symmetry were used to model the micelles in the data interpretation. A hard-core interaction shell of suitable thickness and a screened Coulomb potential of the electric double layer (EDL potential) were alternatively used to represent the long-range repulsive tail of the interaction potential. The Percus Yevick and the Rescaled Mean Spherical Approximation were applied. To compare the data of the two techniques, for each sample, a D(app) was calculated from the SAXS best-fitting geometrical parameters and interparticle structure factor of the micelles. Hence, a fitting procedure involving both the scattering and D(app) data was performed. The interpretation of SAXS spectra does not allow the discrimination between the oblate and the prolate symmetries of the aggregates. On the other hand, the comparison of calculated and experimental D(app) values indicates that the prolate ellipsoid is better suited to represent the micelle shape. Moreover, the agreement between calculated and experimental D(app) values is sensitively better at the lowest NaCl concentration when the EDL potential is used. A rodlike micellar growth and a progressive screening of the electrostatic interactions is testified by the trends of best-fitting parameters as a function of the added electrolyte. 相似文献
45.
R. W. Reiser 《Journal of mass spectrometry : JMS》1969,2(5):467-479
The mechanisms for the major fragmentations obtained with selected substituted uracils are discussed. Interpretation of data was facilitated by use of metastable peaks, high-resolution data, and low-voltage spectra. The major fragmentation obtained with N-alkyl substituted uracils, when the alkyl group contains 2 or more carbons, is due to cleavage of the alkyl substituent. This cleavage is accompanied by a rearrangement of 1 or 2 hydrogens from the alkyl group to the uracil ring. Possible mechanisms for the rearrangements are discussed. It was found that the molecular ion of 1- and 3-alkyl substituted uracils (where the alkyl group has 2 or more carbons) does not undergo the expected ‘retro Diels-Alder Reaction’. Instead, the odd-electron ion formed by loss of the alkyl substituent with a single hydrogen rearrangement undergoes this reaction (loses HNCO). Since it is formed as a secondary reaction product, the relative abundance of the ‘retro Diels-Alder’ fragment is low compared to what is obtained in the spectra of the simple uracils. The ‘retro Diels-Alder Reaction’ can be used to differentiate between 2- and 4-thiouracils, and between 1- and 3-methyl and phenyl substituted uracils. It was found that 1- and 3-alkyl substituted uracils (alkyl group of 2 or more carbons) can be differentiated by the mass of the M-alkyl fragment since the 3-substituted compounds give predominantly a double hydrogen rearrangement and the 1-substituted compound gives mainly a single hydrogen rearrangement. In addition the intensity of the molecular ion, relative to the M-alkyl ion, is considerably stronger in the 1-substituted uracils. 相似文献
46.
Frank J. Millero Sara Sotolongo David J. Stade Carmen A. Vega 《Journal of solution chemistry》1991,20(11):1079-1092
The oxidation of Fe(II) with H2O2 has been measured in NaCl and NaClO4 solutions as a function of pH, temperature T (K) and ionic strength (M, mol-L–1). The rate constants, k (M–1-sec–1), d[Fe(II)]/DT=-k[Fe(II)][2O2]at pH=6.5 have been fitted to equations of the formlog k = log k0+ AI
1/2+BI+CI
1/2/T
Where log k0=15.53-3425/T in water; A=–2.3, –1.35; B=0.334, 0.180; and C=391, 235, respectively, for NaCl (=0.09) and NaClO4 ( =0.08). Measurements made in NaCl solutions with added anions yield rates in the order B(OH)
4
–
>HCO
3
–
>ClO
4
–
>Cl–>NO
3
–
>SO
4
2–
and are attributed to the relative strength of the interactions of Fe2+ or FeOH+ with these anions. The FeB(OH)
4
+
species is more reactive while the FeCO
3
0
, FeCl+, FeNO
3
+
and FeSO
4
0
species are less reactive than the FeOH+ ion pair. The general trend is similar to our earlier studies of the oxidation of Fe(II) with O2 except for B(OH)
4
–
. The effect of pH on the logk was found to be a quadratic function of the concentration of H+ or OH– from pH=4 to 8. These results have been attributed to the different rate constants for Fe2+ (k0) and FeOH+ (k1) which are related to the measured k by, k=k0Fe + k1FeOH, where i is the molar fraction of species i. The rates increase due to the greater reactivity of FeOH+ compared to Fe2+. k0 is independent of composition and ionic strength but k1 is a function of ionic strength and composition due to the interactions of FeOH+ with various anions. 相似文献
47.
Zusammenfassung Mit der beschriebenen gaschromatographischen Anlage kann CS2 in CO2 und inerten Gasen bis zu 1,5 mg CS2/Nm3 (= 0,00002 Vol.-% CS2) quantitativ bestimmt werden. Die Identifizierung erfolgt hierbei über das Durchbruchsvolumen der CS2-Zacke, die quantitative Auswertung über die Fläche der CS2-Zacke, die, mit dem Volumenmaßstab der Abszisse und der reziproken Galvanometerempfindlichkeit multipliziert, der CS2-Menge direkt proportional ist. Der Proportionalitätsfaktor wurde hierbei durch Analysen von CS2-Gasgemischen mit zirka 350 g CS2/Nm3 und einer entsprechenden Verdünnungsreihe ohne Verwendung des Anreicherungssystems erstellt. Die Genauigkeit beträgt bei 5 mg CS2/Nm3 etwa ± 5 Rel.-%.In dem beschriebenen System erfolgt eine Anreicherung auf die etwa 100fache Eingangskonzentration. Diese Anreicherungsmethode könnte auch zur Erhöhung der Empfindlichkeit anderer CS2-Bestimmungsmethoden herangezogen werden.
Summary The gas chromatic apparatus described here permits the quantitative determination of CS2 in CO2 and inert gases down to 1.5 mg CS2/Nm3 (= 0.00002 vol.-% CS2). The identification is accomplished by means of the break-through volume of the CS2 jag, the quantitative measurement through the area of the CS2 jag, which, multiplied by the volume scale of the abscissae and the reciprocal galvonometer sensitivity, is directly proportional to the quantity of CS2. The proportionality factor was plotted through analyses of CS2-gas mixtures with around 350 mg CS2/Nm3 without use of the accumulating system. The accuracy is approximately ± 5 rel.-% at 5 mg CS2/Nm3.
Résumé L'appareillage de chromatographie en phase gazeuse décrit par Les auteurs permet de déterminer le sulfure de carbone dans l'anhydride carbonique et les gaz inertes jusqu'à une teneur de 1,5 mg CS2/Nm3 (soit 0,0002 vol.-% CS2). L'identification résulte de l'évaluation du volume moyen qui correspond au pic du sulfure de carbone et la détermination quantitative est effectuée à l'aide de la surface de ce pic qui, multipliée par le coefficient de volume des abscisses et l'inverse de la sensibilité du galvanomètre est proportionnelle à la quantité de sulfure de carbone. Le facteur de proportionalité est établi par analyse de mélanges gazeux de sulfure de carbone contenant environ 350 g CS2/Nm3 sans utiliser le dispositif d'enrichissement. Pour 5mg CS2/Nm3 la sensibilité atteint environ ± 5% rel.相似文献
48.
Kyle Clagg Sara Hold Archana Kumar Stefan G. Koenig Remy Angelaud 《Tetrahedron letters》2019,60(1):5-7
The direct application of Knochel-Hauser derivative arylmagnesium halides in Kumada-Corriu couplings is described. By utilizing the in situ-generated Grignard reagents, the transmetalation with stoichiometric zinc salts to known Negishi coupling conditions is avoided, thereby streamlining the transformation. Several aromatic hetereocycles participate in the deprotonation and couple with a variety of phenyl iodides and bromides in isolated yields up to 81%. The parent system is demonstrated on 6?g scale with 79% yield, and monitored via ReactIR to show the stability of the Grignard and progression of the deprotonation/CC coupling reaction. 相似文献
49.
Twenty-one R2R′2N+X− -type (R=methyl or ethyl, R′=alkyl, X=Br or I) quaternary ammonium (QA) halides have been prepared by using a novel one-pot synthetic route in which a formamide (dimethyl-, diethylformamide, etc.) is treated with alkyl halide in the presence of sodium or potassium carbonate. The formation of QA halides was verified with 1H-NMR, 13C-NMR, MS and elemental analysis. The crystal structures of four QA halides (two bromide and two iodide) were determined using X-ray single crystal diffraction, and the powder diffraction method was used to study the structural similarities between the single crystal and microcrystalline bulk material. The thermal properties of all compounds were studied using TG/DTA and DSC methods. The smallest compounds decomposed during or before melting. The decreasing trend of melting points was observed when the alkyl chain length was increased. The liquid ranges of 120-180 °C were observed for compounds with 5-6 carbon atoms in the alkyl chain. The low melting points and wide liquid ranges suggest potential applicability of these compounds for example as ionic liquids precursors. 相似文献
50.
A novel procedure for immobilization of liposomes inside fused-silica capillaries is demonstrated. First, the inner wall of the capillaries was coated with a positively charged polymer, composed of derivatized agarose. Subsequently, negatively charged liposomes were immobilized by electrostatic interaction on the polymer coating. The developed liposome coated capillaries were used as a nanoseparation tool for studying interactions between small drug compounds and liposomes. Part of this work was presented at the 15th International Symposium on Microscale Separations and Analysis, HPCE 2002, Stockholm, Sweden, April 2002. 相似文献