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  • 1,2-Thiazetidine 1,1-dioxides  (2)
  • Double-axis rotary shadowing  (1)
  • Flower-specific cDNAs
  • Wiley-Blackwell  (3)
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  • 1
    ISSN: 0170-2041
    Keywords: β-Sultam, 4-acyl-, 4-(α-hydroxylalkyl)- ; 1,2-Thiazetidine 1,1-dioxides ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acylation of N-silylated and 2,3-substituted 1,2-thiazetidine 1,1-dioxides (β-sultams) results in the formation of 4-acylated β-sultams 2 and 8. The desilylation of 2 to 3 is easily done with TBAF either on silica gel or in ethanolic solution. The acylated β-sultams are reduced by sodium borohydride yielding α-hydroxyalkyl β-sultams 11 and 12, obtained as mixtures of diastereoisomers. These are separated by CC. The stereochemistry of the acylated and of the α-hydroxylated β-sultams is elucidated by spectroscopic methods, and compared to that of the antibiotic drug thienamycin.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1992 (1992), S. 687-692 
    ISSN: 0170-2041
    Keywords: β-Sultams ; 1,2-Thiazetidine 1,1-dioxides ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 4-α-Hydroxyalkylated β-sultams 1/5 are transformed into 4-alkylidene-β-sultams 4/7 by elimination and desilylation reactions. Another route to an exocyclic double bond in the β-sultam system has been found to be the Peterson olefination starting from 4 silylated β-sultams 8, 10, and 11. The elimination-reaction sequence yields stereochemically defined products with either E or Z configuration but by use of the Peterson reaction we have always obtained mixtures of diastereomers, which have to be separated. The stereochemistry of all products is elucidated by spectroscopic methods.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Electron Microscopy Technique 18 (1991), S. 440-449 
    ISSN: 0741-0581
    Keywords: High resolution SEM ; Cryomethods ; Double-axis rotary shadowing ; Unidirectional shadowing ; Planar-magnetron sputtering ; Chromium ; Platinum/carbon ; T4 phages ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Natural Sciences in General
    Notes: Structural information on the surface of biological specimens can be resolved within molecular dimensions by “in-lens” field emission scanning electron microscopes when cryo-methods are used to adequately preserve the native state of the specimen. The visual definition of molecular surface structures depends largely on the metal coating. The thickness of the coating, as well as the temperature at which it is deposited, are among the most important parameters affecting visual definition. These were evaluated on T4 polyheads and T4D phages using chromium double-axis rotary shadowing (DARS). Micrographs of optimally DARS coated T4 polyheads and T4D phages were compared with chromium planar-magnetron sputtering (PMS) and unidirectional shadowing with platinum/carbon. Metal deposition was carried out at low temperatures during all three procedures.Optimal visual definition of structural details on the surface of DARS coated T4 polyheads and T4D phages (capsomeres of T4 polyheads and their subunits with diameters of 8 and 3 nm; T4D phage tail fibres with a thickness of 3 nm) is achieved at a thickness of the chromium film greater than the minimum required for metal film coalescence. Chromium DARS coating at room temperature resulted in poor structural definition, whereas DARS at specimen temperatures of -85°C and -150°C, with the chromium thickness optimized for each temperature, yielded good visual detail of polyhead substructures. The visual definition was slightly reduced when DARS coating was carried out at a specimen temperature of -250°C. Adequate structural visibility of T4D phage and T4 polyhead surface structures was achieved with the three coating techniques tested. Smaller filamentous structures, however (e.g., phage tail fibres), were more clearly identified after chromium DARS coating or unidirectional platinum/carbon shadowing than after optimized PMS with chromium. Each method has its own merits.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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