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991.
本文研究涉及差分算子的亚纯函数的唯一性问题,得到一个唯一性定理:设f是一个级不小于2的有限级整函数,η是非零复数,a(z)是不恒等于0的整函数,满足ρ(a)ρ(f)和λ(f-a)ρ(f).若f-a与Δnηf-a(n=1或2)CM分担0,则f(z)是整数级的,且ρ(a)=1或ρ(a)≥ρ(f)-1,f(z)=a(z)+[Δnηa(z)-a(z)]eA(z),其中A(z)是一个次数和ρ(f)相等的多项式. 相似文献
992.
Let G be a graph with vertex set V(G) and edge set E(G). A labeling f : V(G) →Z2 induces an edge labeling f*: E(G) → Z2 defined by f*(xy) = f(x) + f(y), for each edge xy ∈ E(G). For i ∈ Z2, let vf(i) = |{v ∈ V(G) : f(v) = i}| and ef(i) = |{e ∈ E(G) : f*(e) =i}|. A labeling f of a graph G is said to be friendly if |vf(0)- vf(1)| ≤ 1. The friendly index set of the graph G, denoted FI(G), is defined as {|ef(0)- ef(1)|: the vertex labeling f is friendly}. This is a generalization of graph cordiality. We investigate the friendly index sets of cyclic silicates CS(n, m). 相似文献
993.
本文首先由超空间上Cauchy-Pompeiu公式定义了超空间上高阶Teodorescu算子,研究了此类算子的一些基本性质.其次,利用此类算子,我们得到了$k$-超正则函数的Almansi型展开. 最后运用这个展开,我们证明了$k$-超正则函数的Morera型定理、开拓定理和唯一性定理. 相似文献
994.
Yongqiang Zhang ShengzhengWang Zhenyuan Miao Jianzhong Yao Wannian Zhang Chunquan Sheng 《中国化学》2013,(9):1139-1143
Iodiconazole is a novel antifungal agent that was developed in its racemic form. In order to investigate the ef- fects of the chiral center on the antifungal activity, R- and S-isomers of iodiconazole were prepared on the basis of the asymmetric Sharpless epoxidation. (S)-Iodiconazole was proved to have better antifungal activity than the (R)- isomer. The binding modes of the two isomers with lanosterol 14~z-demethylase were clarified by molecular dock- ing. 相似文献
995.
Wei Sun Linjie Tian Hui Qi Dan Jiang Ying Wang Song Li Junhai Xiao Xiaohong Yang 《中国化学》2013,(9):1144-1152
A series of tri-substituted chiral pyrrolidin-2-one derivatives have been designed and synthesized as CC chemokine receptor 4 (CCR4) antagonists. The structure of CCR4 was built by homology modeling. Asymmetric synthesis was applied to synthesize the R,R configuration chiral pyrrolidin-2-one scaffold. The stereoisomeric con- figurations of the compounds were identified by 2D I H-~H COSY spectroscopy and 1D NOESY spectroscopy. This method was more economical and convenient than traditional X-ray single crystal diffraction. In addition, the inter- actions between these compounds and the N-terminal extracellular tail of CCR4 were studied using capillary zone electrophoresis. The CCR4 chemotaxis inhibition effect was tested in CCR4-transfected HEK293 cells. Several compounds showed potent activities as CCR4 antagonists. Among these compounds, lc is the most active one. Its apparent binding constant of CZE experiment result is (1.569±0.11)× 10s L·mol ^-1, and its percentage inhibition of the HEK293/CCR4 cells migration with the concentration of I gmol·L ^-1 in DMSO is 59%. And compound If has slightly higher affinity to N-terminal of CCR4 according to its apparent binding constant than lb because of the in- troduced ester linkage. Further studies on the mechanism of these compounds are in progress. 相似文献
996.
An effcient formal synthesis of(+)-tashiromine was achieved by employing an intermolecular asymmetric Mannich-type reaction as the key step.Concurrently,a novel approach toward the total synthesis of(+)-stemoamide through dyotropic rearrangement of 3,4-cis-b-lactone was also explored. 相似文献
997.
全面整治燃煤小锅炉是大气污染防治行动计划的主要内容之一。业界预计,未来5年该市场需求将达400亿元。全国工商联环境服务业商会秘书长骆建华表示,锅炉脱硫、燃煤改燃气、关停是整治燃煤小锅炉的主要路径。据悉,此前市场普遍认为燃煤锅炉整治的市场将面临资 相似文献
998.
999.