Recent advances in capillary electrophoretic migration techniques for pharmaceutical analysis (2013–2015)

This review updates and follows‐up a previous review by highlighting recent advancements regarding capillary electromigration methodologies and applications in pharmaceutical analysis. General approaches such as quality by design as well as sample injection methods and detection sensitivity are discussed. The separation and analysis of drug‐related substances, chiral CE, and chiral CE‐MS in addition to the determination of physicochemical constants are addressed. The advantages of applying affinity capillary electrophoresis in studying receptor–ligand interactions are highlighted. Finally, current aspects related to the analysis of biopharmaceuticals are reviewed. The present review covers the literature between January 2013 and December 2015.     

Spectroscopic characterization of molybdenum dinitrogen complexes containing a combination of di- and triphosphine coligands: 31P NMR analysis of five-spin systems

The three molybdenum-N2 complexes [Mo(N2)(dpepp)(depe)] (1), [Mo(N2)(dpepp)(dppe)] (2), and [Mo(N2)(dpepp)(1,2-dppp)] (3), all of which contain a combination of a bi- and a tridentate phosphine ligand, were prepared and investigated by vibrational and (31)P NMR spectroscopy. As a tridentate ligand bis(2-diphenylphosphinoethyl)phenylphosphine (dpepp) has been employed. The three different bidentate ligands are 1,2-bis(diethylphosphino)ethane (depe), 1,2-bis(diphenylphosphino)ethane (dppe), and R-(+)-1,2-bis(diphenylphosphino)propane (1,2-dppp). N-N as well as metal-N vibrations of 1-3 are identified and interpreted in terms of the geometric and electronic structures of the complexes. (31)P NMR spectra are recorded and fully analyzed. Moreover, correlation spectroscopy (COSY)-45 measurements are performed to determine the relative signs of coupling constants. Special attention is directed to a detection of different isomers and their (31)P NMR, as well as vibrational spectroscopic properties. The implications of the results for the area of synthetic nitrogen fixation with phosphine complexes are discussed.     

Tandem cyclopropanation with dibromomethane under Grignard conditions

Tertiary Grignard reagents and dibromomethane efficiently cyclopropanate allylic (and certain homoallylic) magnesium and lithium alcoholates at ambient temperature in ether solvents. Lithium (homo)allyl alcoholates are directly cyclopropanated with magnesium and CH2Br2 under Barbier conditions at higher temperatures. The reaction rates depend on the substitution pattern of the (homo)allylic alcoholates and on the counterion with lithium giving best results. Good to excellent syn-selectivities are obtained from alpha-substituted substrates, which are in accord with a staggered Houk model. In tandem reactions, cyclopropyl carbinols are obtained from allyloxylithium or -magnesium intermediates, generated in situ by alkylation of conjugated aldehydes, ketones, and esters as well as from allyl carboxylates or vinyloxiranes. Using this methodology, numerous fragrance ingredients and their precursors were efficiently converted to the corresponding cyclopropyl carbinols.     

Freezing and Melting of Water Confined in Silica Nanopores

In nanosized pores, liquid water can be thermodynamically stable down to temperatures well below the limit of homogeneous nucleation of bulk water (～235 K). Studies of water in such pores therefore offer an opportunity to reveal the anomalous behavior of deeply supercooled water. Herein we focus on recent studies of the limits of freezing and melting of water in the cylindrical pores of ordered mesoporous silicas with pore diameters in the range of 2–10 nm, based on vapor sorption measurements, calorimetric studies, NMR spectroscopy and cryoporometry, and neutron diffraction studies.     

Sulphur substituted organotin compounds : VII. Charge transfer interactions of arylthiomethyl(triphenyl)tin compounds with tetracyanoethylene

Thermolysis of η²-benzoyl(phenyl)zirconocene yields the η²-benzophenonzirconocene complex 2, isolated as a dimer. 2 exhibits an ambivalent reactivity pattern. The formation of five-membered metallacycles from 2 and olefinic hydrocarbons possibly proceeds analogous to reactions of “normal” metalolefin π-complexes. However, both reactions with the electron-deficient olefins dimethylfumarate and -maleate and the behavior towards electrophilic and protic reagents as well as aromatic hydrocarbons might be interpreted in terms of a metallaoxirane-character of 2.     

Free-flow isoelectric focusing of proteins remaining in cell fragments following sonication of thyroid carcinoma cells

The method of preparing protein mixtures for electrophoretic analysis of membrane-associated cell proteins was improved. By sonication, about one-half of the proteins of thyroid cells were released into the supernatant, while the other half preferentially comprising membrane proteins still remained in cell fragments, which could be sedimented by centrifugation. After sonication, even those proteins which remained in cell fragments, could completely be dissolved by free-flow isoelectric focusing media. They migrated through the free-flow electrophoresis chamber without forming precipitates. Because of these improvements, it was possible to show that the two thyroid cancer cell lines ML-1 and ONCO-DG1 express cytokeratin 8 at similar rates, but cytokeratins 7 and 18 differently. In addition, the presence of inorganic pyrophosphatase, tubulin-beta-5, and tubulin-beta-1 chains in human thyroid cells was proved for the first time.     

Ternary systems Sr-{Ni,Cu}-Si: Phase equilibria and crystal structure of ternary phases

Phase relations were established in the Sr-poor part of the ternary systems Sr-Ni-Si (900 °C) and Sr-Cu-Si (800 °C) by light optical microscopy, electron probe microanalysis and X-ray diffraction on as cast and annealed alloys. Two new ternary compounds SrNiSi₃ (BaNiSn₃-type) and SrNi_9−xSi_4+x (own-type) were found in the Sr-Ni-Si system along with previously reported Sr(Ni_xSi_1−x)₂ (AlB₂-type). The crystal structure of SrNi_9−xSi_4+x (own-type, x=2.7, a=0.78998(3), c=1.1337(2) nm; space group P4/nbm) was determined from X-ray single crystal counter to be a low symmetry derivative of the cubic, parent NaZn₁₃-type. At higher Si-content X-ray Rietveld refinements reveal the formation of a vacant site (□) corresponding to a formula SrNi_5.5Si_6.5□_1.0. Phase equilibria in the Sr-Cu-Si system are characterized by the compounds SrCu_2−xSi_2+x (ThCr₂Si₂-type), Sr(Cu_xSi_1−x)₂ (AlB₂-type), SrCu_9−xSi_4+x (0≤x≤1.0; CeNi_8.5Si_4.5-type) and SrCu_13−xSi_x (4≤x≤1.8; NaZn₁₃-type). The latter two structure types appear within a continuous solid solution. Neither a type-I nor a type-IX clathrate compound was encountered in the Sr-{Cu,Ni}-Si systems.Structural details are furthermore given for about 14 new ternary compounds from related alloy systems with Ba.     

Schlüsselreaktionen einer synthese des sibirosamins

[2,3]-Sigmatropic rearrangement and vic. $\text{cis}$-oxyamination of 3-$\text{C}$-methyl-ald-m-enopyranosides are the key steps for the synthesis of a sibirosamine precursor.     

Tetrazole compounds. 10. Novel tetrazolylindoles by fischer indolization of substituted tetrazolylacetaldehyde phenylhydrazones

The acid-catalyzed reaction of substituted phenylhydrazines 1 with 1-aryl-5-(2-dimethylaminovinyl)-1H-tetrazoles 2 afforded (1-aryl-1H-tetrazol-5-yl)acetaldehyde phenylhydrazones 3 which on heating in acetic acid/perchloric acid underwent a Fischer indolization to give substituted 3-(1-aryl-1H-tetrazol-5-yl)-indoles 4a-k. Indoles of this type are also formed on subjecting 1 and 2 directly to indolization conditions; thus, starting from phenylhydrazine the tetrazolylindoles 41-s were obtained by a one-pot procedure. Indolization of corresponding N_α-methylphenylhydrazones 5 resulted in 1-methyl-3-(1-aryl-1H-tetrazol-5-yl)indoles 6 .