Global ETD Search
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Showing 1 to 4 of 4 for “"3-hydroxytetrahydrofuran"”.
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Methacrylate esters of cyclic alcohols of potential biomedical utility
3-Hydroxytetrahydrofuran, 3,4-epoxybutan-1-o1 and 3,4-epoxy-3- methylbutan-1-o1 were synthesized. The corresponding methacrylate esters were also prepared and their spectroscopic data are presented. The commercially available 3-methyloxetan-3- ylmethanol was converted to its methacryloyl ester and …
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Total electron scattering cross sections of molecules containing H, B, C, N, O, F, Si, P, S, and Cl in the energy range 0.1- 6.0 keV.
… (Tetrahydrofuran, Furan, Tetrahydropyran, 3-hydroxytetrahydrofuran, D-Glucose, and alpha-D-glucose), and simple amino acids (Glycine, Lysine and L-histidine) in the energy range 0.1-6.0 keV are predicted using the model. The reliability of these predictions are verified by comparing the …
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Chemoenzymatic routes to enantiopure hydroxytetrahydrofurans: muscarine and its analogues
… and stereoselective transformations of 3-hydroxytetrahydrofuranss. A review of synthetic routes to these compounds is presented, with a particular focus on routes to the natural product muscarine and its analogues. Chapter 2 discusses the preparative routes to the 3-hydroxytetrahydrofurans …
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Photoelectron circular dichroism of anionic chiral metal complexes and deprotonated molecules
… a neutral chiral molecule (fenchone, menthone, 3-hydroxytetrahydrofuran or alaninol) and an atomic gold anion, or deprotonated chiral molecules (alaninol, 1-indanol), which are (in most cases) deprotonated at the hydroxyl group. These chiral systems are massselected and subsequently photodetached …