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排序方式: 共有3396条查询结果,搜索用时 640 毫秒
991.
992.
A wide range of diffractive elements have been used to evaluate the topological charge of Laguerre–Gaussian beams. Here, we show theoretically and experimentally that this charge can be simply and readily measured from the interference pattern in Young’s double-slit experiment. It can be evaluated from the twisting order of the interference. The results are confronted with previously published studies. The potentialities of the method are then compared with existing techniques. 相似文献
993.
994.
Inhibition of Cu‐Amyloid‐β by using Bifunctional Peptides with β‐Sheet Breaker and Chelator Moieties
995.
We consider scattering of a pulse propagating through a three-dimensional random media and study the shape of the pulse in the parabolic approximation. We show that, similarly to the one-dimensional O’Doherty–Anstey theory, the pulse undergoes a deterministic broadening. Its amplitude decays only algebraically and not exponentially in time, due to the signal low/midrange frequency component. We also argue that the parabolic approximation captures the front evolution (but not the signal away from the front) correctly even in the fully three-dimensional situation. 相似文献
996.
997.
David Dailler Dr. Grégory Danoun Benjamin Ourri Prof. Dr. Olivier Baudoin 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(26):9370-9379
A general and scalable access to the aeruginosin family of marine natural products, exhibiting potent inhibitory activity against serine proteases, is reported. This was enabled by the strategic use of two recently implemented Pd‐catalyzed C(sp3)?H activation reactions. The first method allowed us to obtain the common 2‐carboxy‐6‐hydroxyoctahydroindole (Choi) core of the target molecules on a large scale, whereas the second method provided a rapid and divergent access to various hydroxyphenyllactic (Hpla) subunits, including halogenated ones. This unique strategy, together with an optimization of the fragment coupling sequence allowed the synthesis of four aeruginosins, that is, 98A–C and 298A from the chiral pool. Among them, aeruginosin 298A was synthesized on an unprecedentedly large scale. In addition, halogenated aeruginosins 98A and 98C were synthesized for the first time, thanks to a fine‐tuning of the final hydrogenation step. 相似文献
998.
Evelia RasolofonjatovoBret Tréguier Olivier ProvotAbdallah Hamze Estelle MorvanJean-Daniel Brion Mouad Alami 《Tetrahedron letters》2011,52(9):1036-1040
A convenient and efficient procedure for the synthesis of 4-arylchromenes, thiochromenes, and related heterocycles via a four step-sequence has been developed. The first three steps, which involve hydration of alkynes, hydrazones formation, and their Pd-coupling with ortho substituted aryl halides, furnished stereoselectively Z-trisubstituted olefins without any purification of the intermediates generated in each stage. These latter proved to be suitable precursors, in the last step, for the synthesis of the desired heterocycles of biological interest. 相似文献
999.