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81.
In this paper,we study Tingley's problem on symmetric absolute normalized norms on R2.We construct new methods for Tingley's problem on two-dimensional spaces by using isosceles orthogonality,which does not make use of the notion of natural extension.Furthermore,using our methods,several sufficient conditions for Tingley's problem on symmetric absolute normalized norms on R2 are given.As applications,we present various new examples including the two-dimensional Lorentz sequence space d(2)(ω,q) and its dual d(2)(ω,q)*by simple arguments.  相似文献   
82.
A bio‐inspired cascade reaction has been developed for the construction of the marine natural product ageladine A and a de novo array of its N1‐substituted derivatives. This cascade features a 2‐aminoimidazole formation that is modeled after an arginine post‐translational modification and an aza‐electrocyclization. It can be effectively carried out in a one‐pot procedure from simple anilines or guanidines, leading to structural analogues of ageladine A that had been otherwise synthetically inaccessible. We found that some compounds out of this structurally novel library show a significant activity in modulating the neural differentiation. Namely, these compounds selectively activate or inhibit the differentiation of neural stem cells to neurons, while being negligible in the differentiation to astrocytes. This study represents a successful case in which the native biofunction of a natural product could be altered by structural modifications.  相似文献   
83.
New iodotriptycenes, including some chiral derivatives, have been synthesised, and their catalytic potential towards oxidative transformations has been investigated. The enantioselectivities observed in the products using chiral iodotriptycene catalysts are low, probably owing to the large distances between the coordinating groups and the iodine moieties in these compounds.  相似文献   
84.
Sequential sigmatropic rearrangements (Claisen/Claisen and Claisen/Overman) of enantiopure allylic diols are described. The reactions proceeded in complete diastereoselectivity without protecting group manipulations. The sequential Claisen/Overman rearrangement was successfully applied to the total synthesis of (-)-kainic acid.  相似文献   
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Acceleration of Cu(I)-mediated Huisgen 1,3-dipolar cycloaddition (Sharpless ‘click reaction’) by non-basic histidine derivatives was found. An efficient ‘self-activating’ click reaction between the azide- and acetylene-containing peptides on the solid-phase has also been achieved by introducing the Nim-benzylhistidine residue on the reacting peptides.  相似文献   
88.
In discrete Burgers’ equation, time is discretized but space remains continuous. Reduction modulo 2 of discrete Burgers’ equation discretizes also space. This dynamical system generates an elegant pattern known since long time ago. We also propose to show that the Galois groups of particular solutions of Burgers’ equation are abelian. It would imply that the dynamical systems are integrable.  相似文献   
89.
This paper stresses the importance of focusing on the modeling process of computational models for precisely understanding a complex organization and for solving given problems in the organization. Based on our claim, we proposes a method of interpretation by implementation (IbI), which explores factors that drastically change simulation results through an investigation on the modeling process of computational models. A careful investigation on the capabilities of the IbI approach, which comprises the three methods of (a) breakdown and representation, (b) assumption or premise modification, and (c) layer change investigation, derives the following conclusions: (1) the IbI approach has the potential of finding underlying factors that determine the characteristics of an organization; (2) the IbI approach can specify points of attention at necessary levels when analyzing an organization; and (3) the IbI approach has suchadvantages as wide applicability, the effective use of employed models, and KISS principle support.  相似文献   
90.
Novel disilene-iron complexes [(E)- (1E) and (Z)-(eta2-R3SiClSi=SiClSiR3)Fe(CO)4 (1Z), SiR3 = tBu2MeSi] were synthesized by the reaction of the corresponding tetrachlorodisilane with an excess amount of K2Fe(CO)4, and the structures of 1E and 1Z were determined by X-ray crystallography. These complexes constitute not only the first transition-metal complexes with E,Z-isomerism but also the first complexes with halogen-substituted disilene ligands. The initial formation of 1Z during the synthetic reaction and the slow one-way isomerization of 1Z to 1E are rationalized by the intervention of the corresponding silylene complex (R3SiCl2Si)(R3Si)Si=Fe(CO)4.  相似文献   
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