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1.
Alex F. Meindertsma Michael M. Pollard Ben L. Feringa Johannes G. de Vries Adriaan J. Minnaard 《Tetrahedron: Asymmetry》2007,18(24):2849-2858
This paper describes the enantioselective hydrogenation of vinylthioethers. We show that thioether derivatives of maleic esters can be hydrogenated with full conversion and up to 60% ee, and that α-thioether cinnamic acids can be hydrogenated in 51% ee with modest conversion. 相似文献
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The complex forming properties of the thiazole azo dyestuffs and related compounds have been studied in order to try to ascertain the role of importance of the donor atoms present in thiazolylazo-resorcinol. Potentiometric titrations were employed for these determinations, although in many cases meaningful stability constants could not be obtained because of reagent instability or insolubility of the complexes formed on chelation. 相似文献
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Mixtures of cis and trans 1,3-oxazolidin-4-ones were obtained by cyclodehydration, in the presence of p-toluenesulfonic acid or boron trifluoride etherate, of lactamide and N-methyl-lactamide with aromatic and aliphatic aldehydes. The products were separated by column (silica) chromatography and their configurations were determined. 相似文献
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P. M. Pollard J. W. McMillan D. J. Malcolme-Lawes 《Journal of Radioanalytical and Nuclear Chemistry》1982,70(1-2):349-370
Sensitive and selective nuclear reaction methods have been sought for the nuclear microprobe measurement of the spatial distributions
of13C and13C/12C ratios. The13C(α, n)16O reaction, with neutron detection, is the most selective for13C, and has a sensitivity of ca. 100 ppm. The reactions13C(d, p)14C and12C(d, p)13C, with proton detection, are the most sensitive for the simultaneous measurement of13C and12C, with detection limits of 30 and 2 ppm respectively. Less sensitive alternative reaction pairs are;13C(3He, p)15N and12C(3He, p)14N;13C(d, nγ)14N and12C(d, pγ)13C;13C(3He, pγ)15N and12C(3He, pγ)14N. The conditions governing their use, particularly light element interferences, are detailed. 相似文献
8.
An experimental study of the thermal decomposition of a β‐hydroxy alkene, 3‐methyl‐3‐buten‐1‐ol, in m‐xylene solution, has been carried out at five different temperatures in the range of 513.15–563.15 K. The temperature dependence of the rate constants for the decomposition of this compound in the corresponding Arrhenius equation is given by ln k (s?1) = (25.65 ± 1.52) ? (17,944 ± 814) (kJ·mol?1)·T?1. A computational study has been carried out at the M05–2X/6–31+G(d,p) level of theory to calculate the rate constants and the activation parameters by the classical transition state theory. There is a good agreement between the experimental and calculated rate constants and activation Gibbs energies. The bonding characteristics of reactant, transition state, and products have been investigated by the natural bond orbital analysis, which provides the natural atomic charges and the Wiberg bond indices. Based on the results obtained, the mechanism proposed is a one‐step process proceeding through a six‐membered cyclic transition state, being a concerted and slightly asynchronous process. The results have been compared with those obtained previously by us (Struct Chem 2013, 24, 1811–1816) for the thermal decomposition of 3‐buten‐1‐ol, in m‐xylene solution. We can conclude that in the compound studied in this work, 3‐methyl‐3‐buten‐1‐ol, the effect of substitution at position 3 by a weakly activating CH3 group is the stabilization of the transition state formed in the reaction and therefore a small increase in the rate of thermal decomposition. 相似文献
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Abstract Due to the wide use of polymers in medicine, researchers are required to solve a very important problem–to understand the interaction between materials of nonphysiological origin and the surrounding biological liquids, and tissues, particularly blood. 相似文献
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David Pollard 《Annales de l'Institut Henri Poincaré (B) Probabilités et Statistiques》2002,38(6):1039
The paper provides a recursive interpretation for the technique known as bracketing with adaptive truncation. By way of illustration, a simple bound is derived for the expected value of the supremum of an empirical process, thereby leading to a simpler derivation of a functional central limit theorem due to Ossiander. The recursive method is also abstracted into a framework that consists of only a small number of assumptions about processes and functionals indexed by sets of functions. In particular, the details of the underlying probability model are condensed into a single inequality involving finite sets of functions. A functional central limit theorem of Doukhan, Massart and Rio, for empirical processes defined by absolutely regular sequences, motivates the generalization. 相似文献