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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.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) was investigated for arsenic speciation of compounds of environmental interest. It is a very sensitive mass spectrometric technique which can detect as little as 0.3 ng of arsenic or 4 pmol of the arsenical under investigation. This feature suggests that the method could be used for the identification of minor arsenic components in environmental samples. Additional advantages of the technique are its capability of providing molecular ions as well as fragment ions for a variety of arsenicals, and allowing for a certain degree of control in compound fragmentation, by adjusting the N2 laser power. Quantitative analysis by MALDI-TOF-MS is still considered a highly unreliable procedure since many variables associated with sample preparation and analytical procedure can seriously affect the results.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Rapid Communications in Mass Spectrometry 7 (1993), S. 33-36 
    ISSN: 0951-4198
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: The advantages of desorption chemical ionization mass spectrometry (DCI-MS) for characterizing arsenic compounds that exist in the environment include the presence in the spectra of recognizable molecular ions as well as structurally characteristic fragment ions. Satisfactory spectra can be obtained with 100 ng arsenic on the DCI filament, making the technique eminently suitable for the investigation of environmental samples.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 4
    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.
    Type of Medium: Electronic Resource
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  • 5
    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.
    Type of Medium: Electronic Resource
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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.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 2 (1988), S. 263-275 
    ISSN: 0268-2605
    Keywords: Polymer-supported ferrocene derivatives ; 13C CP MAS spectra ; polystyrene polymers ; Mössbauer spectra ; palladium derivatives ; hydrogenation catalysts ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polystyrene derivatives react with the lithioferrocenes Fe(η5-C5H4Li)(η5C5H5),Fe(η5-C5H5),Fe(η5-C5H4Li)2,Fe[η5-C5H3(CHMeNMe2)Li-1,2] [η5-C5H5], and with lithium ferrocenylphosphines, to yield ironcontaining materials. The Mössbauer spectra confirm the loading of unstrained ferrocene fragments, some oxidized, in all cases. The 13C CP MAS NMR spectra also show the loading but the resolution (structural information) is not as good as can be obtained on model solid samples. Palladium(II) derivatives of the amine- and phosphine-containg materials are active hydrogenation catalysts for olefins. Double-bond migration also occurs in the case of 1-hexene.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 8
    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.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 3 (1989), S. 79-87 
    ISSN: 0268-2605
    Keywords: Arsenic compounds ; clams ; speciation ; tetramethylarsonium ion ; arsenobetaine ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The water-soluble arsenic compounds in five species of clams - Butter clam (Saxidomus giganteus), Horse clam (Schizothoerus nuttalli), Soft-shelled clam (Mya arenaria), Native littleneck clam (Protothaca staminea), and Manila clam (Venerupis japonica) - are described. Varying amounts of arsenobetaine and tetramethylarsonium ion are the major arsenicals found in all species. Butter clams show the presence of a third compound which appears to be trimethylarsine oxide. Small amounts of as-yet-unidentified arsenicals can also be isolated.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 10
    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.
    Type of Medium: Electronic Resource
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