Asymmetric Organocatalysis in Complex Target Synthesis: Progress Towards the Total Synthesis of Diazonamide A
<p>Progress towards the total synthesis of the marine natural product diazonamide A is described. The synthesis was conceived around an iminium-catalyzed alkylation/cyclization cascade that stereoselectively installs the central C(10) quaternary carbon stereocenter and the complete furanoindol...
Internet
https://thesis.library.caltech.edu/4288/1/rknowles.pdfKnowles, Robert Randolph (2009) Asymmetric Organocatalysis in Complex Target Synthesis: Progress Towards the Total Synthesis of Diazonamide A. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/40HC-7C37. https://resolver.caltech.edu/CaltechETD:etd-10282008-080437 <https://resolver.caltech.edu/CaltechETD:etd-10282008-080437>