A new projection and contraction method for linear variational inequalities

In this paper, we presented a new projection and contraction method for linear variational inequalities, which can be regarded as an extension of He's method. The proposed method includes several new methods as special cases. We used a self-adaptive technique to adjust parameter β at each iteration. This method is simple, the global convergence is proved under the same assumptions as He's method. Some preliminary computational results are given to illustrate the efficiency of the proposed method.     

Pyrrolothieno[1,4]diazepines part III: Synthesis of amino,hydrazino and mercapto derivatives

Treatment of 2-(2-formyl-1H-pyrrol-1-yl)-3-thiophenecarbonitrile by sodium percarbonate afforded, in a one-pot sequence and on a multigram scale, 5,6-dihydro-6-hydroxy-4H-pyrrolo[1,2-a]thieno-[3,2-f][1,4]diazepin-4-one whose reactivity towards various nucleophiles like amines, hydrazines and thiols was evaluated.     

An expeditious hydroxyamidation of carboxylic acids

Capitalizing on in situ activation with the cyclic phosphonic anhydride PPAA (1), the conversion of carboxylic acids into hydroxamic acids has been reduced to an experimentally simple one-pot operation that addresses the issue of polyacylation without resorting to a large excess of hydroxylamine or to protection. Scope and selectivity were satisfactory with a wide range of substrates, including α,β-unsaturated acids and hydroxyacids.     

A modified inexact operator splitting method for monotone variational inequalities

The Douglas–Peaceman–Rachford–Varga operator splitting methods (DPRV methods) are attractive methods for monotone variational inequalities. He et al. [Numer. Math. 94, 715–737 (2003)] proposed an inexact self-adaptive operator splitting method based on DPRV. This paper relaxes the inexactness restriction further. And numerical experiments indicate the improvement of this relaxation.      

Synthesis and Characterization of New Thiacalix[4]arenes Bearing Semicarbazide and Thiosemicarbazide Fragments at the Lower Rim

Starting from thiacalixarene tetraacetates, tetraacetohydrazides have been prepared and then used for the introduction of semicarbazide and thiosemicarbazide fragments into the lower rim by the reaction with phenyl isocyanate and phenyl isothiocyanate in dry toluene. The structures of the prepared compounds were investigated by FT‐IR, FAB‐MS, ¹H NMR, and X‐ray crystallography, and their receptor properties were examined by liquid liquid extraction of dichromate anions.     

A New Inexactness Criterion for Approximate Logarithmic-Quadratic Proximal Methods

Recently,a class of logarithmic-quadratic proximal(LQP)methods was intro- duced by Auslender,Teboulle and Ben-Tiba.The inexact versions of these methods solve the sub-problems in each iteration approximately.In this paper,we present a practical inexactness criterion for the inexact version of these methods.     

An MEDT study of the mechanism and selectivities of the [3+2] cycloaddition reaction of tomentosin with benzonitrile oxide

The [3+2] cycloaddition (32CA) reaction of tomentosin with benzonitrile oxide yielding a spiro-isoxazoline has been studied within the Molecular Electron Density Theory at the B3LYP/6-31(d,p) computational level. Given the multifunctionality of tomentosin, this 32CA reaction can take place along 16 competitive reaction paths. The chemo-, regio-, and stereoisomeric reaction paths involving the two C C double bonds of tomentosin have been studied. Density functional theory (DFT) calculations account for the total chemo- and regioselectivity, in complete agreement with the experimental outcomes, being suggestive of low diastereofacial selectivity. Analysis of the conceptual DFT indices accounts for the nonpolar character of this 32CA reaction. On the other hand, the topological analysis of the electron localization function of the selected points of the intrinsic reaction coordinate associated with the formation of the C C and C O single bonds emphasizes the zw-type reactivity of the phenyl nitrile oxide; the reaction taking place through a non-concerted two-stage one-step mechanism initialized with the formation of the C C single bond involving the β-conjugated carbon of tomentosin.