Synthetic studies towards the total synthesis of discorhabdin C
Date
1994
Authors
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Abstract
Two synthetic approaches towards the total synthesis of discorhabdin C (3) are described. The general strategy for construction of azacarbocyclic spiro dienone system is to employ an intramolecular para-phenolic alkylation (58 to 43). The key reaction for the first approach is a newly improved aromatic Claisen rearrangement. The key reaction for the second approach is a novel tin-mediated indole synthesis developed in our laboratory.(DIAGRAM, TABLE OR GRAPHIC OMITTED...PLEASE SEE DAI)
Description
Advisor
Degree
Doctor of Philosophy
Type
Thesis
Keywords
Organic chemistry, Biochemistry
Citation
Li, Tangqing. "Synthetic studies towards the total synthesis of discorhabdin C." (1994) Diss., Rice University. https://hdl.handle.net/1911/16751.
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