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Skip to Search Results- 3Nazarov reaction
- 2Alternative Nazarov reaction
- 2Interrupted Nazarov reaction
- 1Allenamide
- 1Allylic alcohol transposition
- 1Domino
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Spring 2013
The five-membered carbocyclic framework is a prevailing structural motif found in natural products and bioactive compounds. Over the years, the Nazarov reaction has been continuously refined as a versatile protocol to access cyclopentanoid products. In this dissertation, several projects built...
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Fall 2014
This dissertation expands the scope and understanding of the Nazarov electrocyclization and interception of the reactive cyclopentenyl cation intermediate that is formed though a 4π electrocyclization of a pentadienyl cation. An intermolecular process for interrupting the Nazarov is discussed....
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Fall 2012
5-Membered carbocycles are ubiquitous in natural products and synthetic drugs. Methods of generating them are therefore valuable, and the ability to do so in a stereospecific and enantioselective manner while making considerable gains in molecular complexity with additional incorporation of...