Rigid tetranitroresorcinarenes

[reaction: see text]. o-alkylation of C2V-symmetrical resorcinarene tetraesters 2 with 2 equiv of 1,3-difluoro-4,6-dinitrobenzene readily affords conformationally rigid octanitro resorcinarene 3, which is a potential scaffold for the design of supramolecular structures.     

Diaza crown ethers bearing heterocyclic ligating groups on nitrogen atoms and their complexing properties with divalent inorganic cations

Two nitrogen-substituted 4,13-diaza-I8-crown-6 compounds, bearing 2-methylquinolyl and 2-methylquinolyl-1-oxide groups, have been prepared. Ionophore-cation selectivities with a range of inorganic divalent cations have been investigated by means of membrane techniques, demonstrating their high selectivity for the Hg(II) cation.     

14-Noreudesmanes and a phenylpropane heterodimer from sea buckthorn berry inhibit Herpes simplex type 2 virus replication

Two new 14-noreudesmane sesquiterpenes, one new phenylpropane heterodimer, caulilexin C, and uvaol were isolated from the 70% MeOH extract of the fruit peel of Elaeagnus rhamnoides. The structures of the compounds were elucidated by HRESIMS and advanced NMR methods. The absolute configuration of (R)-6,9-dihydroxy-1-oxo-14-noreudesm-5,7,9-triene was determined by the TDDFT-ECD method. The new compounds, together with structurally similar naphthalenes (musizin, musizin-8-O-glucoside, torachrysone-8-O-glucoside) and 1,4-naphthoquinone (2-methylstipandrone), isolated previously from Rumex aquaticus, were investigated for their antiviral activity against Herpes simplex virus type 2 (HSV-2) using two different methods. Applying the traditional virus yield reduction test, (R)-6,9-dihydroxy-1-oxo-14-noreudesm-5,7,9-triene, 1-[3-methoxy-4-(2-methoxy-4-(1E)-propenyl-phenoxy)-phenyl]-propane-1,2-diol, and musizin caused a 2.00 log₁₀, 3.49 log₁₀, and 2.33 log₁₀ reduction of HSV-2 yield, respectively, at a concentration of 12.5?μM. 2-Hydroxy-1-methoxy-6,9-dioxo-14-noreudesm-1,3,5(10),7-tetraene exhibited an antiviral effect at concentration of 50?μM only. Similar results were obtained when the qPCR method was used to test the antiviral activity of the compounds.     

Propriétés de l'EDM pour un processus de Poisson d'intensité discontinue

The problem considered is a problem parameter estimation of a 2d-dimensional parameter of a Poisson process. The intensity function of the process is a smooth function with respect to first d variables and is discontinuous function of d other variables. We show the consistency and asymptotic normality of the minimum distance estimator. To cite this article: A.S. Dabye, C. R. Acad. Sci. Paris, Ser. I 342 (2006).     

A synthetic receptor for choline and carnitine

A synthetic receptor is described with the appropriate shape and size for alkylated trimethylammonium ions such as choline and carnitine. The structure features a deep, concave binding site, lined with aromatic walls that provide cation-pi interactions between host and guest. Molecular mechanic calculations suggest that the host's shape is maintained through intermolecular hydrogen bonding with DMSO solvent molecules. The cavity is too small to accommodate larger ions. Choline and carnitine are recognized and bound with high affinity even though no complementary charges are involved in the process.     

New linear integral kinetic parameters assessment method based on an accurate approximate formula of temperature integral

This work concerns a proposition of a new assessment method to obtain kinetic parameters from nonisothermal solid-state kinetics, based on a new and accurate approximate formula of temperature integral. The new formula was derived numerically by a two-step linearly fitting process without using any further approximating series. The relative error involved in the activation energy has been estimated and found to be less than 0.001% in the practical range of 15 < x < 60. A comparison of the suggested approximations to published approximates has shown significant improvements in terms of accuracy at high and low x values. The validity of the new method has been confirmed by computing activation energy from experimental data. Moreover, two approaches have been proposed to determine the kinetic reaction model and preexponential factor based on the new approximate formula. The comparison of the obtained results arising from the application of the present method to others obtained by the most widely reported methods in the literature shows a remarkable preeminence of the new method.     

Water-stabilized cavitands

Tetrabenzimidazole cavitands 4 were prepared by condensation of ortho esters with octaamino cavitand 3 in 70-80% yield. Molecular modeling predicted that no intramolecular hydrogen bonds are possible between the imidazole fragments in the vase conformation of 4. Instead, this conformation provides four perfect binding sites for hydroxyl-containing molecules through an N-H---O-H---N pattern. Such interactions provide the means for sealing the cavitand's cavity. Accordingly, dry compounds 4 are not soluble in dry CDCl3 but readily dissolve upon addition of small amounts of alcohols or by saturation of the solution with water. 1H NMR spectroscopy revealed that in these solutions molecules 4 adopt a vase conformation while 1D GOESY experiments revealed their monomeric nature. In water-saturated CDCl3, these cavitands 4 form kinetically stable 1:1 inclusion complexes with tetramethylphosphonium bromide and triethylammonium chloride in which the cation is incorporated into the pi-basic cavity. Thus, cavitands 4 are a novel class of open-ended molecular containers capable of the formation of highly kinetically stable complexes upon assistance by hydrogen-bonding water molecules.     

Ketenes in polymer-assisted synthesis

Since its inception, ketene chemistry has developed into a unique and well-established source of useful transformations for conventional synthetic organic chemistry. It is, therefore, not surprising that soon after their movement from the realm of peptide and peptoid libraries to that of small molecules, combinatorial chemists have sought the benefits of ketene chemistry to satisfy their own synthetic needs. The ability of these versatile molecules to undergo reactions with nucleophiles, and to participate in cycloadditions and cyclocondensations, has been utilized for the preparation of diverse heterocyclic compounds, and has added to the advantages of polymer-assisted synthesis for rapid purification. Different types of ketenes and different methods for their generation have been involved, which illustrates the potential diversity of the chemistry. There is now a better grasp of the effect of the fragility of these sometimes transient molecules on the reactions involving solid supports, and this augurs well for the application of some of the more recent developments in ketene chemistry to the generation of small-molecule libraries.     

A polymer-bound cavitand

[reaction: see text] An amino-footed cavitand, 1, was attached to an insoluble polystyrene support, and the uptake of organic guest molecules by the resulting polymer 3 from xylene or toluene solutions was achieved.