Synthesis of Nucleic Acid–Peptide Conjugates Targeted to Proteins

Nucleic acid–peptide conjugates have frequently been used to manipulate gene expression in living cells or to facilitate on-array immobilization of peptides or proteins. Recently, it has been recognized that the programmed self-assembly of nucleic acids can be used as a control element to confine the spatial arrangement or the conformation of peptides. This renders the hybrid molecules useful for studies of proteins and protein function, and could allow switching of the bioactivity of the appended peptides and thus the targeted protein by means of nucleic acid hybridization. A prerequisite of such studies is a feasible access to the desired chimeric molecules. This review describes recent efforts in the synthesis of nucleic acid–peptide hybrid molecules.     

Selective Oxidation of Cyclohexane to Cyclohexanone Catalyzed by Phenanthroline–CuCl2 Complex

A highly efficient oxidation of cyclohexane to cyclohexanone is accomplished over phenanthroline–CuCl₂ catalyst in relatively mild conditions. This study realized nearly 100% selectivity for cyclohexanone at 24.4% conversion of cyclohexane. The reaction has been studied by various parameters like performance of copper(II) salts, effect of solvents, influence of bases, the ratio of o-phenanthroline: CuCl₂, and reaction time. In order to further study this reaction system, the possible mechanism was proposed.     

Growth of In2O3 Nanowires Catalyzed by Cu via a Solid–Liquid–Solid Mechanism

In₂O₃ nanowires that are 10–50 nm in diameter and several hundred nanometers to micrometers in length have been synthesized by simply annealing Cu–In compound at a relatively low temperature of 550°C. The catalysis of Cu on the growth of In₂O₃ nanowires is investigated. It is believed that the growth of In₂O₃ nanowires is via a solid–liquid–solid (SLS) mechanism. Moreover, photoluminescence (PL) peaks of In₂O₃ nanowires at 412 and 523 nm were observed at room temperature, and their mechanism is also discussed.     

Synthesis of nano-phase ZrC by carbothermal reduction using a ZrO2–carbon nano-composite

Carbothermal reduction of Zr-sucrose gels powders into nano-phase ZrC, or ZrC-Zr(C,O) core-shell powders, via a composite of 2–4 nm sized ZrO₂ and amorphous carbon, is described. Samples with 1.7–20 sucrose-carbon:Zr ratio gels heated to 1495 °C at 10 °Cmin^?1, with 3 and 30 min hold time were studied in detail using; TG, XRD, SEM, TEM, STEM-EDX, and XPS with Ar⁺-ion etching. After 1495 °C, 3 min, the samples with 12-20C:Zr ratios yielded weakly agglomerated 30 to 40 nm sized ZrC particles, surrounded by a dense 5 nm thick shell of Zr(C,O). With 5C:Zr significant amounts of ZrO₂ was present after heating at 1495 °C for 3 min, while after 30 min annealing, ZrC particles without residual amorphous carbon was obtained. Minor amounts of zirconia was found in most samples, which in similarity with the 5 nm Zr(C,O) shell, is believed to stem from post synthesis oxidation.     

One-Pot Synthesis of Coumarin–Indomethacin Hybrids as COX-2 Targeting Probes for Cancer Imaging

Facile synthesis of 6- or 7-substituted coumarin-indomathacin hybrids (Coum-IDM) has been developed for specific cyclooxygenase-2 (COX-2) binding along with their intrinsic fluorescent properties. A mild and rapid condensation/dehydrative cyclization of 2-hydroxy benzaldehyde with activated indomethacin was carried out in one step under ultrasound irradiation. Coum-IDM₄ was found to be the best of this series as it presented significant binding to COX-2 and exhibited higher fluorescent intensity in cancer cells than in normal cells. Therefore, in the light of drug development tools, this new hybrid system could be a potential targeted probe for COX-2-overexpressed inflammation and cancer-cell tracking.     

Scalable and Selective β-Hydroxy-α-Amino Acid Synthesis Catalyzed by Promiscuous l-Threonine Transaldolase ObiH

Enzymes from secondary metabolic pathways possess broad potential for the selective synthesis of complex bioactive molecules. However, the practical application of these enzymes for organic synthesis is dependent on the development of efficient, economical, operationally simple, and well-characterized systems for preparative scale reactions. We sought to bridge this knowledge gap for the selective biocatalytic synthesis of β-hydroxy-α-amino acids, which are important synthetic building blocks. To achieve this goal, we demonstrated the ability of ObiH, an l -threonine transaldolase, to achieve selective milligram-scale synthesis of a diverse array of non-standard amino acids (nsAAs) using a scalable whole cell platform. We show how the initial selectivity of the catalyst is high and how the diastereomeric ratio of products decreases at high conversion due to product re-entry into the catalytic cycle. ObiH-catalyzed reactions with a variety of aromatic, aliphatic and heterocyclic aldehydes selectively generated a panel of β-hydroxy-α-amino acids possessing broad functional-group diversity. Furthermore, we demonstrated that ObiH-generated β-hydroxy-α-amino acids could be modified through additional transformations to access important motifs, such as β-chloro-α-amino acids and substituted α-keto acids.     

Synthesis of a Ti–Cr–V alloy by pulsed current assisted reaction

Preparations of a Ti–Cr–V alloy were tried by applying pulsed electric current through compacted mixtures of TiO₂, V₂O₅, Cr₂O₃ and C, and of TiH₂, Cr and V after ball-milling into fine powder. TGA and DTA curves for a mixture of TiO₂, V₂O₅, Cr₂O₃ and C showed that weight decreased up to about 1423 K. The Ti–Cr–V alloy could not be prepared from a mixture of TiO₂, V₂O₅, Cr₂O₃ and C. However, from a mixture of TiH₂, Cr and V, the Ti–Cr–V alloy formed together with phases of Cr_1.93Ti_1.07, Ti or C.     

Synthesis of SiC precursors by a two-step sol–gel process and their conversion to SiC powders

A two-step sol–gel processing was developed to synthesize phenolic resin–SiO₂ hybrid gels as SiC precursors, with tetraethoxysilane (TEOS) and novolac phenolic resin being the starting materials, and oxalic acid (OA) and hexamethylenetetramine (HMTA) being the catalysts. At the first step TEOS was prehydrolyzed under the catalysis of OA. At the second step HMTA was added to facilitate gelation. The influences of the molar ratio of OA/TEOS and prehydrolysis time on the sol–gel reaction were investigated. There existed an optimum OA/TEOS ratio where prehydrolysis time needed to form transparent gels was the shortest. The increase of temperature could accelerate sol–gel reaction. The dried hybrid gels were yellowish transparent glassy solids, with uniform microstructure composed of nanometer-sized particles. The conversion of the gels to silicon carbide powders was complete when heated at 1650°C for 30 min in vacuum. The oxygen and free carbon were 0.43 and 0.50 wt%, respectively, in the powder produced from the gel prepared with starting resin/TEOS being 0.143 g/ml.     

Synthesis of mesoporous SiO2–ZrO2 mixed oxides by sol–gel method

A series of SiO₂–ZrO₂ mixed oxides were prepared by sol–gel method in the presence of directing agent, with variable amounts of ZrO₂ between pure silica and pure zirconia, with the aim to obtain catalytic materials suitable as solid acid catalysts. SiO₂–ZrO₂ mixed oxides differ from the two pure starting oxides. While SiO₂ has a low OH density without peculiar acid character, the introduction of increasing amounts of Zr increases the density of the acid sites in the materials. Furthermore both SiO₂/ZrO₂ molar ratio and drying procedure are able to influence the physico-chemical characteristics (textural properties, acid sites distribution, etc.) of these mixed oxides.     

Synthesis and Properties of Lipoamino Acid–Fatty Acid Mixtures: Influence of the Amphiphilic Structure

The acylation of amino acids by acid chlorides with from 8 to 12 carbon atoms in alkaline aqueous medium following Schotten–Baumann reaction results in sodium salts of a N ^α-acylamino acid and fatty acid mixture. The latter are present in a proportion from 40 to 60%. These compositions represent mixtures of amphiphilic anionic surfactants. Together they contribute to the properties of the formulation. Measurements of the surface-active properties of these formulations, such as critical micelle concentration (CMC), surface tension at the CMC (ST), foaming capacity (FC) and foaming stability (FS), show that surfactant mixtures with the longest chain have the most desirable properties. They are comparable to commercial petroleum-based surfactants. Thus, the CMC, ST and CM values of the formulation obtained starting from leucine and dodecanoyl chloride (310 mg/l, 30.1 mN/m and 200%, respectively) are similar to, and even better than, sodium dodecylsulfate (290 mg/l, 39.1 mN/m and 230%, respectively).     

Synthesis of TS-1 by microwave heating of template-impregnated SiO2–TiO2 xerogels

TS-1 was prepared by microwave heating of a SiO₂–TiO₂ xerogel dry-impregnated with the template, TPAOH. A highly crystalline product was obtained within 30 min after microwave irradiation with yields over 90%. These are significant advantages over the TS-1 obtained by conventional oven heating using alkoxide precursors in liquid phase, which requires 1–2 day crystallization time with low product yields. Characterization of the TS-1 obtained was carried out using XRD, SEM, FT-IR, and UV-vis spectroscopy, and catalytic activity was examined for 1-hexene epoxidation using H₂O₂ as oxidant. These studies revealed that the material obtained by microwave heating of the mixed oxide gel shows essentially identical physicochemical properties to those prepared by conventional means.     

Off/on Switching of Electric Current as a Strategy for One-Pot Synthesis of Bromoarylpyridines by Cross-Coupling/ C−H Bromination

An “OFF/ON” electric current switching protocol was developed as a new strategy for one-pot organic synthesis. Suzuki-Miyaura coupling of 2-bromopyridines with arylboronic acids in an electrochemical cell was performed without applying an electric current, and subsequently, the Pd-catalyzed electrochemical C−H bromination was conducted using the already-present Pd catalyst to obtain 2-(2-bromoaryl)pyridines as products. The one-pot synthesis of bromoarenes can also be achieved without adding an external Br source in the second step. Furthermore, an OFF/ON/OFF two-times switching protocol also realized the formation of an N-containing teraryl derivative.     

Highly Site-Selective Epoxidation of Polyene Catalyzed by Metal–Organic Frameworks Assisted by Polyoxometalate

Ectropis obliqua Prout is one of the most severe defoliator insects of tea plants. Sex pheromones method has been widely used for monitoring and controlling the insect pest of E. obliqua Prout due to their relative safety, low cost, and environmental friendliness. However, conventional preparing sex pheromones of E. obliqua Prout has been criticized by the costly and/or low efficiency procedure. Herein, we report a series of Fe-based metal–organic frameworks (MOFs) as efficient heterogeneous catalysts for the site-selective epoxidation of 3Z,6Z,9Z-octadecatriene to its monoepoxides. Particularly, MIL-100(Fe) combined with polyoxometalate (POM) as cocatalyst appears as the best catalyst for the oxidation of 3Z,6Z,9Z-octadecatriene to a high site selectivity to the corresponding 6,7-epoxide with good yields. 3Z,6Z,9Z-octadecatriene and its corresponding 6,7-epoxide are the primary sex pheromone components of the E. obliqua Prout. Significantly, the field bioassay experiments showed that the mixed products were highly effective in attracting E. obliqua Prout male moths. This work provides a general method to fast and clean synthesis of sex pheromones and opens new avenues for the application of Fe-based MOFs in the pest control with environmental friendliness.