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Skip to Search Results- 1(+)-ipalbidine
- 1Assymmetric synthesis
- 1Asymmetric carbocycle synthesis
- 1Baylis-Hillman
- 1Conjugate additions
- 1Diels-Alder reactions
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Fall 2011
The first chapter of this thesis describes the development of an asymmetric route to the core structure of the indolizidine alkaloids and its application to the total synthesis of (+)-ipalbidine, a member of this compound class. The initial approach was designed to use the intramolecular...
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Intramolecular conjugate displacement for making carbocycles and studies on the total synthesis of MPC1001
DownloadFall 2011
The first chapter of this thesis describes methodology on an all-carbon intramolecular conjugate displacement between a carbon nucleophile and a Morita-Baylis-Hillman adduct for making carbocyclic skeletons. The reaction scope was examined with different electron-withdrawing groups, types of...