I. A1,3-Strain Enabled Retention of Chirality During Bis-Cyclization of β-Ketoamides: Asymmetric Synthesis and Bioactivity of Salinosporamide A and Derivatives II. Optimization of an Organic Syntheses: Asymmetric Nucleophile-Catalyzed Aldol- Lactonization of Aldehyde Acids
The potential of human 20S proteasome inhibitors continues to be of interest for anticancer chemotherapy and the recent FDA approval of bortezomib (Velcade) validates the proteasome as a target for cancer chemotherapy. Salinosporamide A, a marine unique bicycle [3.2.0] Beta-lactone-containing natura...
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2013
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| Online Access: | http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-9035 http://hdl.handle.net/1969.1/148462 |