Development of a Synthetic Strategy Toward Trans-Cyclobutane-Containing Natural Products: Enantioselective Total Synthesis of (+)-Psiguadial B

Development of a Synthetic Strategy Toward Trans-Cyclobutane-Containing Natural Products: Enantioselective Total Synthesis of (+)-Psiguadial B

<p>Trans-cyclobutane-containing meroterpenoids are a structurally intriguing class of natural products with a diverse array of pharmacologically interesting properties. Herein, the development of a synthetic strategy for de novo construction of the trans-cyclobutane motif is described, which h...

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Bibliographic Details
Main Author: Chapman, Lauren Marie
Format: Others
Published: 2017
Online Access:https://thesis.library.caltech.edu/10274/13/Chapman_Lauren_M_2017_Thesis.pdf
Chapman, Lauren Marie (2017) Development of a Synthetic Strategy Toward Trans-Cyclobutane-Containing Natural Products: Enantioselective Total Synthesis of (+)-Psiguadial B. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/Z90G3H5M. https://resolver.caltech.edu/CaltechTHESIS:06052017-010024254 <https://resolver.caltech.edu/CaltechTHESIS:06052017-010024254>

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https://thesis.library.caltech.edu/10274/13/Chapman_Lauren_M_2017_Thesis.pdf
Chapman, Lauren Marie (2017) Development of a Synthetic Strategy Toward Trans-Cyclobutane-Containing Natural Products: Enantioselective Total Synthesis of (+)-Psiguadial B. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/Z90G3H5M. https://resolver.caltech.edu/CaltechTHESIS:06052017-010024254 <https://resolver.caltech.edu/CaltechTHESIS:06052017-010024254>

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