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The regioselective anti-carboindation of ynamides by using InBr3 and silylated nucleophiles was developed to synthesize (Z)-β-(carbonylamino)alkenylindiums. The X-ray crystallographic analysis of an alkenylindium suggested that the reaction proceeded in an anti-addition fashion. In contrast to reported syn-carbometalations of ynamides by using organometallics, a cooperation of InBr3 and silylated nucleophiles to ynamides achieved an anti-addition, which was supported by DFT calculations. The scope of substrates included various ynamides and silylated nucleophiles, such as silyl ketene acetals and silyl ketene imines. The transformation of synthesized alkenylindiums by iodination, radical coupling, and Pd-catalyzed cross-coupling successfully afforded trisubstituted enamines with high regio- and stereoselectivities.  相似文献   
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Jung  Ho Yun  Kim  Chang Heon  Kim  Kyoungmin  Kwon  Soonhak 《The Ramanujan Journal》2022,57(4):1253-1275
The Ramanujan Journal - In this article, we prove that a space of cusp forms of weight 2 with level N and real character $$\chi $$ has dimension 1 if and only if $$\chi $$ is trivial and N is in...  相似文献   
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Crosslinking can fundamentally change the mechanical properties of a linear glassy polymer. It has been experimentally observed that when lightly crosslinked, poly(methyl‐methacrylate) (PMMA) has a characteristically more ductile response to mechanical loading than does linear PMMA despite having a higher glass transition temperature. Here, molecular dynamics (MD) simulations are used to investigate conformational and energetic differences between linear PMMA and lightly crosslinked PMMA under shear deformation. As consistent with experiments, crosslinked PMMA is found to have a reduced yield stress relative to linear PMMA. Using the probing capabilities of our explicit atom MD approach, it is observed that while the crosslinks have a minimal direct energy contribution to the total system, they can alter how the main chains conform to macroscopic loading. In crosslinked PMMA, the backbone aligns more with the direction of external loading, thereby reducing the force applied to (and associated deformation of) the polymer bonds. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014 , 52, 444–449  相似文献   
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The Ramanujan Journal - Let p be a prime. We define S(p) the smallest number k such that every positive integer is a sum of at most k squares of integers that are not divisible by p. In this...  相似文献   
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Major issues in the pharmaceutical industry involve efficient risk management and control strategies of potential genotoxic impurities (PGIs). As a result, the development of an appropriate method to control these impurities is required. An optimally sensitive and simultaneous analytical method using gas chromatography with a mass spectrometry detector (GC–MS) was developed for 19 alkyl halides determined to be PGIs. These 19 alkyl halides were selected from 144 alkyl halides through an in silico study utilizing quantitative structure–activity relationship (Q-SAR) approaches via expert knowledge rule-based software and statistical-based software. The analytical quality by design (QbD) approach was adopted for the development of a sensitive and robust analytical method for PGIs. A limited number of literature studies have reviewed the analytical QbD approach in the PGI method development using GC–MS as the analytical instrument. A GC equipped with a single quadrupole mass spectrometry detector (MSD) and VF-624 ms capillary column was used. The developed method was validated in terms of specificity, the limit of detection, quantitation, linearity, accuracy, and precision, according to the ICH Q2 guideline.  相似文献   
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The facile synthesis of silica supported platinum nanoparticles with ultrathin titania coating to enhance metal-support interactions suitable for high temperature reactions is reported, as thermal and structure stability of metal nanoparticles is important for catalytic reactions.  相似文献   
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Reported here is the Pd‐catalyzed C–N coupling of hydrazine with (hetero)aryl chlorides and bromides to form aryl hydrazines with catalyst loadings as low as 100 ppm of Pd and KOH as base. Mechanistic studies revealed two catalyst resting states: an arylpalladium(II) hydroxide and arylpalladium(II) chloride. These compounds are present in two interconnected catalytic cycles and react with hydrazine and base or hydrazine alone to give the product. The selectivity of the hydroxide complex with hydrazine to form aryl over diaryl hydrazine was lower than that of the chloride complex, as well as the catalytic reaction. In contrast, the selectivity of the chloride complex closely matched that of the catalytic reaction, indicating that the aryl hydrazine is derived from this complex. Kinetic studies showed that the coupling process occurs by rate‐limiting deprotonation of a hydrazine‐bound arylpalladium(II) chloride complex to give an arylpalladium(II) hydrazido complex.  相似文献   
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