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The Synthesis of 6,6'-Binaphthopyran-2-one Natural Products and Synthetic Progress Towards Chrysophaentins A & E

Posted on:2014-02-05Degree:Ph.DType:Thesis
University:University of California, DavisCandidate:Grove, Charles IFull Text:PDF
GTID:2451390005492929Subject:Organic Chemistry
Abstract/Summary:
Natural product synthesis is a complex array of different methodologies used to construct a single molecule. Described herein is a detailed approach towards two different classes of natural products. Chapters one and two focus on the synthesis of 6,6'-binaphthopyran-2-one natural products utilizing a key vanadium-catalyzed oxidative biaryl coupling to access these axial chiral molecules. Chapter three focuses on the synthetic progress towards a class of macrocyclic and linear E-chloroalkene natural products. The latter, although unfinished, has provided crucial insight into the synthetic feasibility of these natural products.
Keywords/Search Tags:Natural, Synthetic progress towards, Synthesis
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