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Synthetic studies of 1,4,5,16-tetrahydroxytetraphenylene.

by Man Fai Shek. / Thesis (M.Phil.)--Chinese University of Hong Kong, 2002. / Includes bibliographical references (leaves 86-90). / Abstracts in English and Chinese. / Chapter I. --- ABSTRACT --- p.1 / Chapter II. --- ACKNOWLEDGEMENTS --- p.4 / Chapter III. --- CONTENT PAGE --- p.5 / Chapter IV. --- INTRODUCTION --- p.6 / Chapter A. --- CHEMISTRY OF TETRAPHENYLENES --- p.6 / Chapter B. --- CLATHRATE INCLUSION CHARACTER OF TETRAPHENYLENES --- p.8 / Chapter C. --- SYNTHESIS OF TETRAPHENYLENE AND SUBSTITUTED TETRAPHENYLENES --- p.10 / Chapter 1. --- ELECTROPHILIC AROMATIC SUBSTITUTION APPROACH --- p.10 / Chapter 2. --- SUBSTITUTED BIPHENYLENE PYROLYSIS APPROACH --- p.12 / Chapter 3. --- ARYL-HALJDE COUPLING APPROACH --- p.14 / Chapter 4. --- BIS ACETYLENE APPROACH --- p.16 / Chapter D. --- "SYNTHESIS OF TRIBENZO[α, c, e]CYCLOOCTENE" --- p.18 / Chapter E. --- "SYNTHESIS OF SUBSTITUTED TRJBENZO[α,c,e]CYCLOOCTENE" --- p.21 / Chapter F. --- THE AIM OF THE PRESENT WORK --- p.25 / Chapter V. --- RESULTS AND DISCUSSION --- p.27 / Chapter 1. --- "SYNTHETIC STUDIES OF 1,4,5,16-TETRAHYDROXYTETRAPHENYLENE FROM 1,4- DIHYDROANTHRAQUINONE" --- p.27 / Chapter 2. --- SYNTHETIC STUDIES OF 1,4,5,16-TETRAHYDROXYTETRAPHENYLENE FROM1- AMINOANTHRAQUINONE --- p.41 / Chapter 3. --- "SYNTHETIC STUDIES OF 1,4, 5,16-TETRAHYDROXYTETRAPHENYLENE FROM 1,8- DIHYDROXYANTHRAQUINONE" --- p.46 / Chapter VI. --- CONCLUSION: --- p.53 / Chapter VII. --- EXPERIMENTAL --- p.57 / Chapter VIII. --- REFERENCES --- p.86 / Chapter IX. --- APPENDIX --- p.91

Identiferoai:union.ndltd.org:cuhk.edu.hk/oai:cuhk-dr:cuhk_324085
Date January 2002
ContributorsShek, Man Fai., Chinese University of Hong Kong Graduate School. Division of Chemistry.
Source SetsThe Chinese University of Hong Kong
LanguageEnglish, Chinese
Detected LanguageEnglish
TypeText, bibliography
Formatprint, 159 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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