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Showing 1 to 4 of 4 for “"anionic oxy-cope"”.
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Evaluation of camphor derivatives in terpenoid synthesis
… to (+)-5,6-dehydro-camphor (36) and subsequent anionic oxy-Cope rearrangement of the resulting 1,5-diene (64) provided hydrindenone 66. Ring expansion of 66 provided decalin intermediate 69 which contains the A/B ring system common to many terpenoids; however, the stereo-specific introduction of …
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Cycloaddition-fragmentation mediated pathways to ring D modified 19-norsteroids
… on cycloaddition of methyl vinyl ketone to 3-methoxyestra-1,3,5(10),14,16-pentaen-17-yl acetate which proceeded with a high degree of regio- and stereoselectivity to give 16α-acetyl-3-methoxy-14, 17α-ethenoestra-1 ,3,5(1 O)-trien-17β-yl acetate. The cycloadduct underwent base mediated …
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Synthesis and structure-activity relationships of ring D alkyl 19-norsteroids
… this investigation, 17β-tert-butyldimethylsilyloxyestra-1,3,5(10),14-tetraen-l6-one was synthesised as starting material for alkylation experiments. Estrone 3-methyl ether was converted into the derived 17β-hydroxy 16-ketone by standard methods. This conversion involved the introduction of a …
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Enantioselective Syntheses and Chemical Investigations of Plant-Derived Bioactive Volatile Compounds
Research, inspired by nature, provides ample opportunity for discovery, ingenuity, and creative endeavor. For these reasons, the work and accomplishments presented herein focus on the total syntheses and related investigations of a variety of natural product derivatives, specifically (+)-nootkatone …