高效和可重复使用的Zr-MCM-41催化剂催化Strecker反应合成氨基腈类化合物(英文)

The synthesis and characterization of Zr-MCM-41 nanoreactors and their catalytic activity in the synthesis of new amino nitrile derivatives by the Strecker reaction in high yields and in short reaction times is reported.     

Catalytic oxidation of urazoles and bis-urazoles to their corresponding triazolinediones using aluminium nitrate and a catalytic amount of silica sulfuric acid

Abstract  

A simple and efficient catalytic oxidation of urazoles and a bis-urazole to the corresponding triazolinediones by treatment with Al(NO₃)₃.9H₂O in the presence of a catalytic amount of silica sulfuric acid is described. A good range of urazole derivatives was selectively oxidized in CH₂Cl₂ at room temperature in good to excellent yields.     

H2SO4/Silicagel: Highly Efficient Catalyst for the Synthesis of α-Aminonitriles Using Trimethysilyl Cyanide

Summary. The multicomponent Strecker reaction using trimethylsilyl cyanide was performed at room temperature and α-aminonitriles were prepared in excellent yields in the presence of a catalytic amount of H₂SO₄ adsorbed on silica gel.     

Interaction of dimethyltin(IV) dichloride with 5′‐IMP and 5′‐UMP

The formation constants of the species formed in the systems H⁺ + dimethyltin(IV) + 5′‐IMP and 5′‐UMP, H⁺ + 5′‐IMP and H⁺ + 5′‐UMP have been determined in aqueous solution in the pH range 1.5–9.5 at constant temperature (25 °C) and constant ionic strength (0.1 mol dm⁻³ NaClO₄), using spectrophotometric and potentiometric techniques. ¹H and ³¹P NMR investigations in aqueous solution confirmed the species formation. The precipitated complexes of IMP and UMP by Me₂Sn(IV)²⁺ at low pH values were characterized by elemental analysis and FTIR spectroscopy methods, the bonding sites of the ligands were determined and ruled out purine and pyrimidine moieties (N‐7 and N‐1 in IMP and N‐3 in UMP, respectively) while a bidentated coordination of the phosphate group is concluded in both cases. Finally, the experiments revealed the existence of complexes with trigonal bipyramidal structures that is in agreement with similar systems resulted previously. Copyright © 2008 John Wiley & Sons, Ltd.     

Fabrication of chain-like Mn2O3 nanostructures via thermal decomposition of manganese phthalate coordination polymers

A novel manganese coordination polymer [Mn(Pht)(H₂O)]_n as a precursor was obtained by chemical precipitation involving an aqueous solution of anhydrous manganese acetate and phthalate anion as a potential O-banded ligand. Fourier transform infrared (FT-IR) results proved that phthalate anions coordinate to metal cations as a chelating bidentate ligand, making polymeric structure. The Mn₂O₃ nanostructures have been prepared via thermal decomposition of as-prepared manganese phthalate polymers as precursor in the presence of oleic acid (OA) and triphenylphosphine (TPP) as a stabilizer and capping. Different approaches such as FT-IR, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were applied to characterize the products. TEM images and XRD analysis indicated that the as-synthesized chain-like Mn₂O₃ has a crystal phase of cubic syngony with a mean size of ∼40 nm.     

Rapid and efficient synthesis of 4(3H)-quinazolinones under ultra sonic irradiation using silica-supported Preyssler nano particles

A new synthesis of 4(3H)-quinazolinone from the reaction of 2-amino-benzamide, and acylchlorides in the presence of catalytic amounts of silica-supported Preyssler nano particles as green, reusable and efficient catalyst under ultra sonic irradiation is reported.     

A combination of molecular docking,receptor-guided QSAR,and molecular dynamics simulation studies of S-trityl-l-cysteine analogues as kinesin Eg5 inhibitors

Structural Chemistry - Kinesin Eg5 plays an essential role in the early stages of mitosis, and it is an interesting drug target for the design of potent inhibitors. In this work, combined molecular...     

Lipid-DNA conjugates for cell membrane modification,analysis, and regulation

ABSTRACT

Lipids and DNAs are two major building blocks of life. Interestingly, by chemically linking these two natural compounds together, synthetic lipid-DNA conjugates exhibit several attractive features for cell membrane studies. These lipid-DNA conjugates are amphiphilic macromolecules combining the cell membrane insertion capability of lipids with the properties of DNAs in precise hybridization and programmability. These supramolecular conjugates have demonstrated exciting applications from generating cell membrane nanopores to transmembrane cargo deliveries, and from analyzing cell membrane events to tissue engineering. In this review, we will discuss the design, structures, and biological applications of lipid-DNA conjugates, with an emphasis on their functions on live cell membranes. We expect, in the near future, significant advancement in our ability to understand, control, and apply these cell membrane-modified lipid-DNA conjugates.     

One-pot synthesis of 1-amidoalkyl-2-naphthols catalyzed by nano-BF3·SiO2

1-Amidoalkyl-2-naphthols were prepared via one-pot multi-component reaction of 2-naphthol, aldehydes, and amides in the presence of nano-silica supported boron trifluoride (nano-BF₃·SiO₂) in ethyl acetate at 80 °C. Short reaction times, high yields, scaleup and easy work-up are the advantages of this protocol.     

A survey of interactions in crystal structures of pyrazine‐based compounds

The important role of pyrazine (pz) and its derivatives in fields such as biochemistry and pharmacology, as well as in the study of magnetic properties, is surveyed. Recognition of these properties without extensive investigations into their structural properties is not possible. This review summarizes interactions that exist between these organic compounds by themselves in the solid state, as well as those in coordination polymers with metal ions and in polyoxometalate‐based hybrids. Complexes based on pyrazine ligands can generate metal–organic framework (MOF) structures that bind polyoxometalates (POMs) through covalent and noncovalent interactions. Some biological and magnetic properties involving these compounds are considered and the effect of hydrogen bonding on their supramolecular architectures is highlighted.