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Showing 1 to 3 of 3 for “"Cyclitols"”.

  1. cis-Arenediols as versatile chiral synthons in the synthesis of prostaglandins, cyclitols, carbohydrates, and alkaloids

    The oxidation of simple benzene derivatives by a mutant of Pseudomonas putida, called 39-D, produces cis-arenediols (1). The diols are enantiomerically pure and can be used as synthons for the preparation of a variety of interesting compounds because of their stereochemistry and the special array …

    vt Repository record for cis-Arenediols as versatile chiral synthons in the synthesis of prostaglandins, cyclitols, carbohydrates, and alkaloids (opens in a new tab)

  2. Molecular modeling studies on the reduction of inososes and deoxy-inososes: a synthetic and historical overview of the cyclitols

    The inososes are a group of compounds, containing six-membered rings that have five hydroxyls (four for the deoxyinososes) and a carbonyl. Due to the relative ease of their reduction to inositols, a study aimed at the potential preparation of these useful natural products was undertaken. The …

    vt Repository record for Molecular modeling studies on the reduction of inososes and deoxy-inososes: a synthetic and historical overview of the cyclitols (opens in a new tab)

  3. The Reactions of Ethyl Ethoxymagnesiomalonate With Some Simple Aliphatic Diacid Chlorides.

    … the biochemical and pharmacological interest in cyclitols, alone, and in combination with other molecules, the biosynthesis of these compounds has been studied in a number of laboratories. Kiely and Sherman recently developed a chemical model which describes the proposed mechanism for the …

    uab Repository record for The Reactions of Ethyl Ethoxymagnesiomalonate With Some Simple Aliphatic Diacid Chlorides. (opens in a new tab)