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  • 1
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 1042-7163
    Schlagwort(e): Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Synthesis and reactions of optically active phosphine-boranes have been investigated. Optically active secondary phosphine-boranes, (Sp)-and (Rp)-menthyloxyphenylphosphine-boranes, and (S)-methylphenylphosphine-borane underwent palla-dium(0)-catalyzed electrophilic arylation with o-, m-, or p-iodoanisole. The stereochemistry of this arylation was largely dependent on the solvent and the base used. The reaction in acetonitrile proceeded with almost complete retention of configuration at the chiral phosphorus, whereas inversion of configuration was observed in ethereal solvents or toluene. The phosphorus-oxygen bond of (Rp)-menthyloxy (methyl) phenylphosphine-borane and (SP)-menthy-loxy(o-methoxyphenyl)phenylphosphine-boranewas reductively cleaved at -78°C by lithium naphtha-lenide or Li/NH3 with virtually net retention of configuration at phosphorus, providing secondary or tertiary phosphine-boranes in excellent yields. New synthetic routes to optically pure C2-symmetric bisphosphine-boranes possessing chirality at phosphorus have been developed on the basis of these stereochemical studies.
    Zusätzliches Material: 3 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Yeast 11 (1995), S. 801-808 
    ISSN: 0749-503X
    Schlagwort(e): pombe ; ras1 protein ; GTP binding ; GTPase ; ATP binding ; Life and Medical Sciences ; Genetics
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: Schizosaccharomyces pombe contains single ras oncogene homologue, ras1, that functions in the signal transduction pathway conducting the cell's mating processes. To understand the biochemical basis of yeast ras proteins, we have purified the ras1 protein and compared the major biochemical constants with those of RAS2 protein from Saccharomyces cerevisiae and mammalian ras proteins. The purified ras1 protein showed a remarkably high Kd value for GDP binding (178 nM) and for binding with ATP. In contrast, the Kd value for GTP binding and the rate of GTPase activity were 64 nM and 77 × 10-6 s-1 at 37°C, respectively; both were higher than normal p21ras protein, but at the same level as the RAS2 protein. We directly measured rate of GTP binding and GDP binding which were 3.9 × 10-3 s-1 and 1.8 × 10-3 s-1 at 30°C, respectively. On the other hand, exchange rates between bound and free nucleotides remained almost constant throughout the tested combination of GTP and GDP, and were several-fold lower than the binding rate. These results suggest that the release of the guanine nucleotide is the rate-limiting step in the ras-GTP/GDP cycle. As a whole, the biochemical properties of the ras1 protein are close to those of the RAS2 protein, although these two proteins function differently in the signal transduction pathway in the cells.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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