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  • Nitromethane addition  (1)
  • Spiro compounds  (1)
  • 1
    ISSN: 1434-193X
    Keywords: Heterocycles ; Carbohydrates ; Imidazolidines ; Oxazolidines ; Spiro compounds ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---Prochiral 1,3-dihydroxyacetone forms racemic oxazolidine- and oxazoline-type spiro[4.4]nonanes upon reactions with potassium (thio)cyanate and cyanamide. In contrast, 1,3-diaminoacetone yields only the corresponding spiro-bisimidazolidinethione under similar conditions together with monocyclic by-products, but the spiro-bisimidazolidinone is accessible by reaction of 1,3-dichloroacetone with urea. The resolution of the racemic spiro-bisoxazolidinethione 2a was achieved by using brucine as the resolving agent.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0170-2041
    Keywords: Nitromethane addition ; Henry reaction ; Carbohydrates ; Fischer-Sowden reaction ; Alditols ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of Nitromethane to Aldoses. - A Comprehensive Study of the Diastereoselectivity of the Fischer-Sowden Reaction by the Help of 13C-NMR Spectroscopy1)The addition of nitromethane to aldoses, commonly referred to as „Fischer-Sowden reaction“, is not as stereoselective as can be concluded from the literature. This is the outcome of a comprehensive study which covered besides glyceraldehyde all aldotetroses, -pentoses and -hexoses. The ratio of the pair of diastereomeric nitroalditols has been determined in each case by 13C-NMR spectroscopy. Thus, incidentially, a whole set of spectral data for all tetritols, pentitols, hexitols and heptitols with a terminal nitro group has been obtained, which can be correlated systematically to the respective data for the parent alditols. From these results follows that at least under conditions which give high yields of products, the reaction is thermodynamically controlled; thus, the product ratio is determined by the different energy content of the product nitroalditols (or their nitronates), which is a result of different patterns of steric interactions between substituents.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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