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Synthetic studies towards calystegine analogues.

Tse, Hon Man. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2008. / Includes bibliographical references (leaves 87-89). / Abstracts in English and Chinese. / Acknowledgment --- p.I / Table of Contents --- p.II / Abstract --- p.III / Abstract (Chinese Version) --- p.IV / Abbreviation --- p.V / Chapter 1. --- Introduction --- p.1 / Chapter 1.1 --- Calstegine --- p.1 / Chapter 1.2 --- "1,3-Dipolar Cycloaddition" --- p.5 / Chapter 1.3 --- Intramolecular Nitrone-alkene Cycloaddition (INAC) --- p.7 / Chapter 2. --- Results and Discussion --- p.14 / Chapter 2.1 --- Introduction --- p.14 / Chapter 2.2 --- INAC of Unbranched Hept-6-enoses derived form D-xylose --- p.15 / Chapter 2.2.1 --- "Hept-6-enose derived from 1,3-Diol 80" --- p.19 / Chapter 2.2.2 --- "Hept-6-enose derived from l,3-Diol 82" --- p.21 / Chapter 2.2.3 --- "Hept-6-enose derived from 1,2-Diol 81" --- p.23 / Chapter 2.2.4 --- "Hept-6-enose derived from 1,2-Diol 83" --- p.27 / Chapter 2.2.5 --- Hept-6-enose derived from 93 --- p.30 / Chapter 2.3 --- INAC of Unbranched Hept-6-enoses derived form L-arabinose --- p.33 / Chapter 3. --- Conclusion --- p.39 / Chapter 4. --- Experimental --- p.42 / Chapter 5. --- References --- p.87 / Appendix-Data of X-ray crystallography / Appendix-NMR Spectra

Identiferoai:union.ndltd.org:cuhk.edu.hk/oai:cuhk-dr:cuhk_326277
Date January 2008
ContributorsTse, Hon Man., Chinese University of Hong Kong Graduate School. Division of Chemistry.
Source SetsThe Chinese University of Hong Kong
LanguageEnglish, Chinese
Detected LanguageEnglish
TypeText, bibliography
Formatprint, vi, 89 leaves : ill. ; 30 cm.
RightsUse of this resource is governed by the terms and conditions of the Creative Commons “Attribution-NonCommercial-NoDerivatives 4.0 International” License (http://creativecommons.org/licenses/by-nc-nd/4.0/)

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