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  • 1
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Employing thujone-derived intermediates, a series of achiral (9a-d; Scheme 1) and chiral (11b and 11d; Scheme 2) terpene analogues related to the biologically active ‘terpenoid’ hybrids have been prepared. The stereochemistry of the key epoxidation reaction was established by correlation of the product 11b with the previously reported alcohol (R)-20 of known absolute configuration (Scheme 3).
    Additional Material: 1 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 6 (1992), S. 179-183 
    ISSN: 0268-2605
    Keywords: Organoarsenic ; diffusion ; liposomes ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Efflux studies of radio-labelled methylarsonic acid (MMA) and dimethylarsinic acid (DMA) encapsulated in liposomes afford the following permeability values for the two arsenicals: 1.4 × 10-13 cm s-1 and 4.5 × 10-11 cm s-1 for MMA and DMA, respectively. These data are compared with the octanol/water partition coefficients which are 7.4 × 10-3 and 8.4 × 10-3 for MMA and DMA, respectively.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 3 (1989), S. 351-353 
    ISSN: 0268-2605
    Keywords: molluscs ; shells ; arsenicals ; antimony ; organotin ; speciation ; methylarsenicals ; butyltin ; mass spectrum ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Inorganic arsenic(III) and arsenic(V), methyl-arsenicals, antimony(III), and antimony(V), and butyltin derivatives are present in the shells of molluscs found in the coastal waters of British Columbia.
    Additional Material: 1 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 3 (1989), S. 515-521 
    ISSN: 0268-2605
    Keywords: Catharanthus roseus ; NMR spectra ; arsenic compounds ; alkaloid metabolites ; methylarsenicals ; uptake ; growth ; methylation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Catharanthus roseus cells were grown in the presence of arsenite, arsenate, methylarsonate and dimethylarsinate. Cell growth and arsenical uptake were monitored. Reduction of arsenate, methylation of arsenic and demethylation of methylarsenic species are described. Alkaloid production by the cells is dramatically influenced by the presence of arsenicals. 1H NMR studies of methylarsonate uptake by whole cells of C. roseus are reported.
    Additional Material: 9 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 8 (1994), S. 463-471 
    ISSN: 0268-2605
    Keywords: Arsenic ; organic arsenic ; C. roseus ; cells ; NMR ; biomolecules ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H spin-echo NMR spectroscopy of intact cells of C. roseus facilitates monitoring changes inside the cells on treatment with arsenicals. This in situ detection method is non-invasive and non-destructive in comparison to other available biochemical methods. Short term uptake of the arsinicals, methylarsinate MMA and dimethylarsenate DMA, by C. roseus cells that have reached stationary phase in 1-B5 medium, is followed by using NMR spectroscopy, and in particular, the Carr-Purcell-Meiboom-Gill pulse sequence. An increase in the peak height of the methylarsenic resonance over a period of 11 h is indicative of uptake of each arsenical. However, there is no evidence of any biotransformation products in the 1H NMR spectra. The accumulation site of DMA is probably the vacuole as is seen from the change in the chemical shift of DMA as it moves into a compartment of lower pH. Biochemical changes associated with the presence of arsenicals are evident in the 1H NMR spectra of C. roseus cells isolated at different stages in the growth cycle. Although uptake has been demonstrated by other analytical techniques, the resonances corresponding to both MMA and DMA are not observed in the 1H NMR spectra of cells growing in media containing each arsenical. The association of these arsenicals with large biomolecules in the cell may account for these absences. In this event, the spins-spin relaxation time of the arsenic species would shorten and the signals would not be seen in the spin-echo NMR spectrum. In cells growing in the presence of MMA, a new resonance is observed at a chemical shift position 2.2 ppm after 15 days of growth. The shift in position of the resonance, from 1.75 ppm expected at physiological pH, may indicate an altered environment around the arsenic species such as high intracellular acidity.
    Additional Material: 8 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 4 (1990), S. 581-590 
    ISSN: 0268-2605
    Keywords: Butyltin species ; cyclohexyltin species ; Plictran ; Cyhextin ; oysters ; seawater ; surface microlayer ; HPLC AA ; GC MS ; HPLC MS ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A HPLC/GF AA procedure based on the use of C-18 columns is described for the quantitation of butyltin species in marine samples. When a mass spectrometer was used as detector (HPLC MS), evidence was obtained for the presence of other tin compounds in the samples. Extracts of samples were treated with CH3MgBr and examined by using GC MS; the presence of BunSnMe4-n (n = 3-1, Bu = butyl) and CynSnMe4-n (n = 3,2, Cy = cyclohexyl) was confirmed in the derivatized seawater, bivalve flesh, and bivalve shell samples. Quantitative data are given for butyl- and cyclohexyl-tin species in seawater and the surface microlayer, and oyster flesh.
    Additional Material: 5 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 1 (1987), S. 1-6 
    ISSN: 0268-2605
    Keywords: Hydrogenation ; Reduction ; Catalystff ; Palladium ; Ferrocenylphosphanes ; Styrenes ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cationic palladium(II) complexes of ferrocenylphosphines [(L-L′)Pd(S)2][ClO4]2 ((L-L′) = Fe(η5-C5H4P (C6H5)2)2 1, or Fe(η5-C5H5)(η5C5H3(CHMeNMe2)P(C6H5)2-1,2) 2a: S=pyridine or dimethylformamide) were prepared and characterized. The derivatives of 2a are effective catalysts for the hydrogenation of simple olefins at 30°C (1 atm H2). The rate of reduction of styrene depends on the substrate concentration, catalyst concentration and the solvent, and is only slightly inhibited (16%) by the addition of mercury. These observations are conistent with a homogeneous catalytic system.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 2 (1988), S. 479-482 
    ISSN: 0268-2605
    Keywords: Trimethylarsine oxide ; biological reduction ; trimethylarsine ; micro-organisms ; methylation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Trimethylarsine oxide [(CH3)3AsO] has been shown to be easily reducible by various biological species, including both aerobic and anaerobic micro-organisms, some skin organisms, soil bacteria, sludge and rumen fluid. The results suggest an enhanced mobility for arsenic owing to facile production of the volatile (CH3)3As species.
    Additional Material: 3 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 3 (1989), S. 401-409 
    ISSN: 0268-2605
    Keywords: Organoarsenic species ; environmental ; HPLC ; thermospray mass spectra ; arsenosugar ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Biologically important arsenic species such as arsenobetaine, arsenocholine iodide, tetramethylarsonium iodide, methylarsonic acid, and dimethylarsinic acid can be separated and quantitated by HPLC. The pH-sensitive separations on a weak anion-exchange column are described, as well as separations on a reverse-phase column with the aid of tetrabutylammonium nitrate or heptanesulfonic acid as ion-pairing agents. The thermospray mass spectra of these arsenicals in addition to those of sodium arsenate and an arsenosugar derivative are described. This technique is suitable for HPLC MS studies.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 8 (1994), S. 313-324 
    ISSN: 0268-2605
    Keywords: Arsenic species ; arsenic uptake ; arsenic methylation ; Polyphysa peniculus ; arsenic bioaccumulation ; non-reducible arsenicals ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polyphysa peniculus was grown in artificial seawater in the presence of arsenate, arsenite, monomethylarsonate and dimethylarsinic acid. The separation and identification of some of the arsenic species produced in the cells as well as in the growth medium were achieved by using hydride generation-gas chromatography-atomic absorption spectrometry methodology. Arsenite and dimethylarsinate were detected following incubation with arsenate. When the alga was treated with arsenite, dimethylarsinate was the major metabolite in the cells and in the growth medium; trace amounts of monomethylarsonate were also detected in the cells. With monomethylarsonate as a substrate, the metabolite is dimethylarsinate. Polyphysa peniculus did not metabolize dimethylarsinic acid when it was used as a substrate. Significant amounts of more complex arsenic species, such as arsenosungars, were not observed in the cells or medium on the evidence of flow injection-microwave digestion-hydride generation-atomic absorption spectrometry methodology. Transfer of the exposed cells to fresh medium caused release of most cell-associated arsenicals to the surrounding environment.
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