Intramolecular 1,3-dipolar cycloaddition of cyclo-1,3-diene-tethered nitrile oxides

Intramolecular 1,3-dipolar cycloaddition of cyclo-1,3-diene- and -1,3,5-triene-tethered nitrile oxides gave tricyclic isoxazolines as a single stereoisomer in most cases. The relative stereochemistry of tricycle-fused isoxazolines resulting from 1,3-dipolar cycloaddition of cyclo-1,3-diene-tethered nitrile oxides is cis-cis, whereas from cyclohepta-1,3,5-triene-tethered nitrile oxides the cis-trans isomer predominates.     

Electron depleted bis(methylene)cyclobutenes: sulfinyl and sulfonyl substitution

Double [2,3] sigmatropic rearrangements of bis(propargyl sulfenates) to bis(allenic sulfoxides) and of bis(propargyl sulfinates) to bis(allenic sulfones) are shown to be a convenient and effective method for the preparation of conjugated diallene systems bearing two electron withdrawing trihalomethyl sulfoxide or sulfone substituents either on C-1 and C-6, or on C-3 and C-4. Such substituents are further shown to facilitate cyclization to bis(methylene)cyclobutenes, and to stabilize the latter. The electron withdrawing group substitution on the exocyclic methylene extremities proved more effective than similar substitution on the endocyclic double bond.     

Zinc mediated reductive dimerization and cyclization of α,β-unsaturated ketones in the presence of a catalytic amount of mercury(II) chloride

The zinc mediated reductive dimerization and cyclization of α,β-unsaturated ketones gives functionalized cyclopentanols in good yield in the presence of a catalytic amount of mercury(II) chloride in N,N-dimethylformamide as solvent at room temperature. The reaction is regio- and stereo-selective producing 3,4-trans-diarylcyclopentanols selectively.     

Superpositions of chiral states in the presence of electric dipole, magnetic dipole, and electric quadrupole interactions

This paper is a straightforward generalization of Maierle-Harris proposal regarding parity implications on the superpositions of chiral states of a molecule. It is shown that the inclusion of electric quadrupole and magnetic dipole interactions removes several of restrictions on the preparation of superpositions of mid R:L and mid R:R states of a chiral molecule. It is also found that the dephasing of mid R:L and mid R:R superpositions, due to the spontaneous emission from the chiral molecule, has opposing contributions from electric quadrupole-magnetic dipole and electric dipole interactions.     

Copper dipyridine dichloride as a mild and efficient catalyst for a one pot condensation bigenelli reaction

The condensation reaction of aldehydes, β‐ketoesters and urea/thiourea in presence of a catalytic amount of CuPy₂Cl₂ complex proceeded under very mild reaction conditions in high yield (80‐90%).     

Functionalized Organotellurium Halides: Synthesis,Characterization, and Observation of Intra- and Intermolecular Secondary Bonding

Abstract

Activated tellurium, but not selenium, reacts with para-substituted benzoylmethyl bromides as well as with iodoacetamide at their melting points in absence of a solvent to give bis(p-substituted benzoylmethyl)tellurium dibromides, (p-YC₆H₄COCH₂)₂TeBr₂, (Y = H, Me, and MeO) and bis(acetamido)tellurium diiodide, (H₂NCOCH₂)₂TeI₂, respectively. Quick reduction of (p-YC₆H₄COCH₂)₂TeBr₂, with sodium metabisulphite in a two-phase system yields crystalline (p-YC₆H₄COCH₂)₂Te. These tellurides undergo smooth oxidative addition of halogens, interhalogen ICl or a pseudohalogen (SCN)₂. Intramolecular coordination of the carbonyl group in these functionalized diorganotellurium dihalides is evident from IR spectra and shorter Te···O (carbonyl) distances in comparison to the sum of van der Waals radii and completes six coordination around Te atom. Not unexpectedly, therefore, intermolecular secondary bonding effects of the type Te…O, Te···X and X···X are missing in (PhCOCH₂)₂TeBr₂, (p-MeOC₆H₄COCH₂)TeBr₂ and (PhCOCH₂)₂TeI₂. Instead, these compounds provide rare examples, among organotellurium compounds, of supramolecular architecture, where C–H···Br and C–H···O hydrogen bonds and π-π (phenyl ring) interactions appear to be the noncovalent intermolecular associative forces that dominate the crystal packing.     

Highly sensitive LC-MS/MS-ESI method for simultaneous quantitation of albendazole and ricobendazole in rat plasma and its application to a rat pharmacokinetic study

A highly sensitive and specific LC-MS/MS-ESI method was developed for simultaneous quantification of albenadazole (ABZ) and ricobendazole (RBZ) in rat plasma (50 μL) using phenacetin as an internal standard (IS). Simple protein precipitation was used to extract ABZ and RBZ from rat plasma. The chromatographic resolution of ABZ, RBZ and IS was achieved with a mobile phase consisting of 5 m m ammonium acetate (pH 6) and acetonitrile (20:80, v/v) at a flow rate of 1 mL/min on a Chromolith RP-18e column. The total chromatographic run time was 3.5 min and the elution of ABZ, RBZ and IS occurred at 1.66, 1.50 and 1.59 min, respectively. A linear response function was established for the ranges of concentrations 2.01-2007 and 6.02-6020 ng/mL for ABZ and RBZ, respectively. The intra- and inter-day precision values for ABZ and RBZ met the acceptance as per FDA guidelines. ABZ and RBZ were stable in battery of stability studies, viz. bench-top, auto-sampler and freeze-thaw cycles. The developed assay was applied to a pharmacokinetic study in rats.     

Five coordinate complexes of N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamide with copper Crystal and molecular structures of dichloro(N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamido)copper(II) and chloro(perchlorato)(N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamido)copper(II)

The title compound N,N,N′,N′-tetraethylpyridine-2,6-dicarboxamide (DEAP) forms a 1:1 complex with anhydrous CuCl₂, [Cu(DEAP)Cl₂], (1) which was crystallized from EtOH solution in the monoclinic space group P2_{1/ n} with cell constant, a = 10.024(1); b = 13.122(1); c = 14.404(1) Å β = 101.31(1)° V = 1857.8(3) ų and Z = 4. The chloro-perchlorato complex, [Cu(DEAP)Cl(ClO₄)], (2) obtained in near quantitative yield by reacting (1) with an excess of NaClO₄ in EtOH, crystallized in the monoclinic space group P2_{1/ n} with cell constants, a = 7.965(1); b = 25.827(2); c = 10.046(1) Å β = 98.81(1)° V = 2042.2(4) ų and Z = 4. Both (1) and (2) contain 5-coordinated copper linked to DEAP through O～N～O donor set of atoms with covalently bonded chlorine atoms in (1) and chlorine and perchlorate groups in (2). The coordination geometry is intermediate between square pyramidal and trigonal bipyramidal, and is probably best described as a trigonally distorted rectangular pyramid.     

Coordination chemistry and biological activity of two tridentate ONS and NNS Schiff bases derived from S-benzyldithiocarbazate

Two tridentate Schiff bases having ONS and NNS donor sequences were prepared by condensing S-benzyldithiocarbazate (NH₂NHCSSCH₂Ph) (SBDTC) with pyridine-2-carboxaldehyde and salicylaldehyde, respectively. Complexes of these ligands with Ni^II, Zn^II, Cr^III, Co^II, Cu^II, and Sn^II were studied and characterized by elemental analyses and various physico-chemical techniques. Ni^II, Cu^II, Zn^II and Sn^II complexes were four-coordinate while the Cr^III, Sr^III and Co^III complexes were six-coordinate. The ONS Schiff base was moderately active against leukemia, while its zinc, antimony and cobalt complexes were strongly active against leukemic cells with DC₅₀ = 0.35–5.00.     

Reactions of cyclopalladated azobenzenes with xanthates and dithiocarbamates. Spectral characterisation and electrochemical studies of the products

Binuclear chloro-bridged cyclopalladated azobenzenes [Pd(A)Cl]₂ (A = ortho-metallated azobenzene or its derivatives) have been reacted with aqueous AgNO₃ to yield aquo-derivatives followed by the addition of xanthates, or dithiocarbamates (RCS₂ ^–) to synthesise ternary complexes, [Pd(A)(RCS₂)]. These complexes occur as configurational isomers and their compositions have been established by ¹H-n.m.r. spectroscopy. Cyclic voltammetric studies show azo reduction at negative and thiol oxidation at positive potentials relative to s.c.e., respectively. Dissociation of RCS₂ ^– under the electrode field is chemically supported by using a sulfide extractor, HgCl₂, Hg(OAc)₂, or AgOAc, to precipitate out the binuclear [Pd(A)Cl]₂/[Pd(A)(OAc)]₂ complexes.