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The condensation of phenols with aromatic hydroxy-aldehydesSousa, Julian Bernard. January 1953 (has links)
published_or_final_version / Chemistry / Master / Master of Science
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The condensation of phenols with deactivated aromatic aldehydes莫秀芬, Mok, Sau-fun. January 1955 (has links)
published_or_final_version / Chemistry / Master / Master of Science
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Development of electrochemical and microbial sensing systems for detection of phenolic compoundsBifulco, Laura January 2002 (has links)
No description available.
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Synthetic studies towards anthraquinonesMitchell, Anthony Stewart, mikewood@deakin.edu.au January 1994 (has links)
The oxidation of substituted phenols with phenyliodonium diacetate in methanol was found to afford 2,4-cyclohexadienones, 2,5-cyclohexadienones or mixtures of isomers depending on the substrate being oxidized. A reaction mechanism was proposed for this oxidation which involved an intermediate aryloxenium ion. A strong correlation was observed between the experimentally determined product ratios and the results predicted by calculation of the LUMO coefficients of the proposed intermediates,
Annulation of these cyclohexadienones with the anion derived from cyanophthalide afforded substituted anthraquinones in high yields. The chemistry relating to the annulation of Michael acceptors with phthalide anions was comprehensively reviewed.
A mild selective method for the oxidation of hydroquinones to quinones using dibenzoyl peroxide and base is presented.
A general synthetic approach to C-glycosylanthraquinones was presented, based on the annulation of a C-glycosylcyclohexadienone with the anion derived from cyanophthalide, A suitable precursor to a C-glycosylcyclohexadienone, 2-(2,3,4,6-tetra-0-acetyl-|3-D-glucopyranosyl)benzyloxybenzene, was prepared via the reaction of benzoylbromoglucose with 2-benzyloxyphenylmagnesium bromide,
A group of molecules were prepared by a Marschalk reaction between /ewcoquinizarin and aldehydo-sugsrs. These compounds are potential bioreductive alkylating agents in which molecular simplicity can be achieved without overly sacrificing DNA binding ability.
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The condensation of phenols with aromatic hydroxy-aldehydes /Sousa, Julian Bernard. January 1953 (has links)
Thesis (M. Sc.)--University of Hong Kong, 1953. / References: p.93-95. Type-written copy.
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The condensation of phenols with deactivated aromatic aldehydes /Mok, Sau-fun. January 1955 (has links)
Thesis (M. Sc.)--University of Hong Kong, 1955. / References: p.102-106. Type-written copy.
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Interactions of carbohydrates with phenolic compoundsZhu, Fan, 朱帆 January 2010 (has links)
published_or_final_version / Biological Sciences / Doctoral / Doctor of Philosophy
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The Liebermann test for phenolsCoffer, Hobert Lowell Dale, 1920- January 1948 (has links)
No description available.
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Indophenol as a product of the Liebermann reactionAshmore, Richard D. January 1950 (has links)
No description available.
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The decomposition of indophenolDuke, Don Carl, 1928- January 1955 (has links)
No description available.
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