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91.
Nicholas A. Weires Yuriy Slutskyy Larry E. Overman 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(25):8649-8653
An alkoxycarbonyl radical cyclization–cross‐coupling cascade has been developed that allows functionalized γ‐butyrolactones to be prepared in one step from simple tertiary alcohol‐derived homoallylic oxalate precursors. The reaction succeeds with aryl and vinyl electrophiles and is compatible with heterocyclic fragments in both coupling partners. This chemistry allows for the rapid construction of spirolactones, which are of interest in drug discovery endeavors. 相似文献
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Ewa Szajdzinska-Pietek Ren Maldonado Larry Kevan Richard R. M. Jones 《Journal of colloid and interface science》1986,110(2)
Electron spin echo modulation studies with a series of x-doxylstearic acids (x = 5, 7, 10, 12, and 16) have been carried out for sodium- and tetramethylammonium dodecylsulfate and dodecyltrimethylammonium chloride frozen micellar solutions containing protiated and perdeuterated 1-butanol. Modulation effects due to nitroxide interactions with deuterium in water and butanol have been measured versus doxyl group position. The effect of 1-butanol on the micellar surface and internal micellar structure has been evaluated and the average location of 1-butanol in these micelles has been deduced to be in the outer annulus of the micelle core. 相似文献
94.
Jiaxin Han Dr. Larry Hoteite Prof. Dr. Joseph P. A. Harrity 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(56):e202201595
The first useful enantioselective Pd-catalyzed asymmetric allylic alkylation of α-fluoro-β-ketoesters has been achieved using the Trost family of chiral ligands yielding products in up to 92 % ee. This work provides new insights regarding the typically modest selectivities associated with acyclic α-fluoroenolates and shows experimental evidence that the typically poor levels of enantiocontrol associated with these systems are not necessarily due to the presence of E/Z enolate mixtures. Finally, this methodology allows the easy preparation of useful 3-fluoropiperidine intermediates, and it is demonstrated that these systems are applicable to a range of functionalization reactions leading to new building blocks for the discovery of bioactive products. 相似文献
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The sensitive detection of sulfur-containing analytes is of interest in many industrial applications; selective detection is also desirable since these compounds are usually present at trace levels in difficult matrixes. The purpose of this article is to review the use of the Sievers® ozone-based sulfur chemiluminescence detector, and its coupling with gas chromatography, supercritical fluid chromatography, and high performance liquid chromatography. Detection limits, linearity, response factors, and selectivity are discussed for each of these techniques. Critical operational parameters for the SCD are also described. The use of other sulfur selective detectors for SFC and HPLC is also briefly summarized. 相似文献
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Moon G. Kim Yimin Wu Larry W. Amos 《Journal of polymer science. Part A, Polymer chemistry》1997,35(15):3275-3285
A wood adhesive-type phenol–formaldehyde (PF) resol resin synthesized with a typical formaldehyde to phenol mol ratio of 2.10 was thoroughly cured and studied by the solid-state crosspolarization/magic angle spinning 13C nuclear magnetic resonance (CP/MAS NMR) spectroscopy. The methylene group/phenol mol ratio values found were between 1.35 and 1.46, close to the value of a completely cured PF polymer structure. The amount of formaldehyde emitted during resin curing was very small. Other formaldehyde-derived groups determined from CP/MAS NMR spectra and relatively high levels of oxidation products of formaldehyde determined from water extracts of cured resin raised the total formaldehyde-derived groups/phenol mol ratio value to close to that of the synthesis mol ratio. Technological implications of these findings are discussed. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 3275–3285, 1997 相似文献