Ferric(III) Nitrate Supported on Kieselguhr: A New Reagent for Selective Oxidation of Alcohols

A selective and effective oxidation of alcohols into the corresponding aldehydes and ketones, respectively, with a new reagent, ferric(III) nitrate supported on kieselguhr, under heterogeneous conditions is reported.     

Oxidation of Alcohols with a New Neutral System of Potassium Dichromate in Dimethylformamide

A new and convenient procedure for the preparation of aldehydes and ketones by the oxidation of the corresponding primary and secondary alcohols with a neutral potassium dichromate-dimethylformamide system is described.     

A facile one-pot, three-component synthesis of 3,3′-(4-arylpyridine-2,6-diyl)bis(2H-chromen-2-one) derivatives under microwave irradiation

A series of 3,3′-(4-arylpyridine-2,6-diyl)bis(2H-chromen-2-one) derivatives have been synthesized by the one-pot, three-component reaction of 3-acetylcoumarin, an aromatic aldehyde, and ammonium acetate in acetic acid under microwave irradiation. This procedure has the major advantages of short reaction time, good yields, low energy consumption, easy operation, and environmental friendliness. All of the products were characterized by IR and NMR spectroscopy, MS, and elemental analysis.     

Consistent Riccati Expansion for Integrable Systems

A consistent Riccati expansion (CRE) is proposed for solving nonlinear systems with the help of a Riccati equation. A system having a CRE is then defined to be CRE solvable. The CRE solvability is demonstrated quite universal for various integrable systems including the Korteweg–de Vries, Kadomtsev–Petviashvili, Ablowitz–Kaup–Newell–Segur (and then nonlinear Schrödinger), sine‐Gordon, Sawada–Kotera, Kaup–Kupershmidt, modified asymmetric Nizhnik–Novikov–Veselov, Broer–Kaup, dispersive water wave, and Burgers systems. In addition, it is revealed that many CRE solvable systems share a similar determining equation describing the interactions between a soliton and a cnoidal wave. They have a common nonlocal symmetry expression and they possess a formally universal once Bäcklund transformation.     

线性变换的特征多项式诱导的直和分解

从线性变换的特征多项式的因式分解入手,研究由特征多项式诱导的全空间的若干种直和分解,得到Jordan标准形理论的一个几何证明,全空间关于线性变换不可分解的刻画以及只存在平凡的不变子空间的刻画.     

Practical and Highly Selective C?H Functionalization of Structurally Diverse Ethers

A trityl ion mediated C H functionalization of ethers with a wide range of nucleophiles at ambient temperature has been developed. The reaction displays high chemoselectivity and good functional group tolerance. The protocol also exhibits excellent regio‐ and diastereoselectivities for the unsymmetric ethers, thus stereoselectively generating highly functionalized disubstituted 2,5‐trans tetrahydrofurans (THF), 2,6‐trans tetrahydropyrans (THP), 2,6‐trans dihydropyrans (DHP), and 1,3‐trans isochromans, and highlighting the capacity of the protocol in complex molecule synthesis.     

Frontispiz: Mild and Versatile Nitrate‐Promoted C?H Bond Fluorination

A novel and facile C H bond fluorination proceeds under remarkably mild conditions (close to room temperature in most cases). Both aromatic and olefinic C(sp²) H bonds with a wide range of electronic properties are selectively fluorinated in the presence of a catalytic amount of simple, cheap, and nontoxic nitrate as the promoter. A Pd^II/Pd^IV catalytic cycle that is initiated by an in situ generated cationic [Pd(NO₃)]⁺ species was proposed based on preliminary mechanistic studies.     

Selected Thoughts on Hydrophobicity in Drug Design

The fundamental aim of drug design in research and development is to invent molecules with selective affinity towards desired disease-associated targets. At the atomic loci of binding surfaces, systematic structural variations can define affinities between drug candidates and biomolecules, and thereby guide the optimization of safety, efficacy and pharmacologic properties. Hydrophobic interaction between biomolecules and drugs is integral to binding affinity and specificity. Examples of antiviral drug discovery are discussed.     

Elucidating dynamic behavior of synthetic supramolecular polymers in water by hydrogen/deuterium exchange mass spectrometry

A comprehensive understanding of the structure, self-assembly mechanism, and dynamics of one-dimensional supramolecular polymers in water is essential for their application as biomaterials. Although a plethora of techniques are available to study the first two properties, there is a paucity in possibilities to study dynamic exchange of monomers between supramolecular polymers in solution. We recently introduced hydrogen/deuterium exchange mass spectrometry (HDX-MS) to characterize the dynamic nature of synthetic supramolecular polymers with only a minimal perturbation of the chemical structure. To further expand the application of this powerful technique some essential experimental aspects have been reaffirmed and the technique has been applied to a diverse library of assemblies. HDX-MS is widely applicable if there are exchangeable hydrogen atoms protected from direct contact with the solvent and if the monomer concentration is sufficiently high to ensure the presence of supramolecular polymers during dilution. In addition, we demonstrate that the kinetic behavior as probed by HDX-MS is influenced by the internal order within the supramolecular polymers and by the self-assembly mechanism.