Development of Iminium-Activation Technologies and the Total Synthesis of (+)-Frondosin B

Development of Iminium-Activation Technologies and the Total Synthesis of (+)-Frondosin B

<p>The enantioselective imidazolidinone-catalyzed epoxidation of α,β-unsaturated aldehydes has been accomplished via a novel 1,4-heteroconjugate addition reaction using hypervalent iodine reagents. Development of an “internal syringe pump” protocol for the slow release of iodosobenzene from an...

Full description

Bibliographic Details
Main Author: Lee, Sandra
Format: Others
Published: 2008
Online Access:https://thesis.library.caltech.edu/5246/1/thesis-SL.pdf
Lee, Sandra (2008) Development of Iminium-Activation Technologies and the Total Synthesis of (+)-Frondosin B. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/83M6-7R38. https://resolver.caltech.edu/CaltechETD:etd-08132007-171008 <https://resolver.caltech.edu/CaltechETD:etd-08132007-171008>

Internet

https://thesis.library.caltech.edu/5246/1/thesis-SL.pdf
Lee, Sandra (2008) Development of Iminium-Activation Technologies and the Total Synthesis of (+)-Frondosin B. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/83M6-7R38. https://resolver.caltech.edu/CaltechETD:etd-08132007-171008 <https://resolver.caltech.edu/CaltechETD:etd-08132007-171008>

Similar Items