School of Chemistry - Theses

Permanent URI for this collection

http://hdl.handle.net/11343/301

Filters

2018 1
Reset filters

Settings
Statistics
Citations
Type: Masters Coursework thesis × Author: Robertson, Angus × End date: 2018 × Subject: total synthesis ×

Search Results

Now showing 1 - 1 of 1
  • Item
    Thumbnail Image
    It’s hip to be square: a cyclobutene diester approach to alkyl citrate natural products
    Robertson, Angus ( 2018)
    This thesis features an enatiospecfic synthesis of a key alkyl citrate retron that was leveraged in the total syntheses of squalene synthase inhibitors (-)-CJ-13,982, (-)-CJ-13,981 and (-)-L-731,120 (featured in Org. Let. 2018, 20, 4255–4258). This key retron was prepared in 7 linear steps, requiring only 4 purification, with a 40% yield from (S)-(+)-γ-hydroxymethy-γ-butyrolactone. The synthesis highlights the application of a formal [2+2] cycloaddition and a remarkable acid-mediated rearrangement sequence to furnish the correct stereochemistry and oxidation level of the citrate moiety. This thesis demonstrates the shortest enantiospecifc total synthesis of (-)-CJ-13,981 to date, via the use of this key citrate retron, affording this natural product in 7.7% total yield over 10 steps. Efforts towards the squalene synthase inhibitor (-)-L-731,120 and the viridiofungins, a family of serine palmitoyl transferase inhibitors that have activity inhibiting hepatitis C replication, are also featured.