
%0 Journal Article
%A Perlmutter, Patrick 
%A Selajarern, Walailak 
%T The NARC-Based Approach to the Enantioselective Synthesis of the Zaragozic Acids. Synthesis of a C 5-Alkoxycarbonyl-Substituted 2,8-Dioxabicyclo[3.2.1]octane.
%J Australian Journal of Chemistry
%D 2000/07/21
%V 53
%N 4
%P 349-353
%K Aldol; anti-cholesterol; bicyclic acetal; heterocycle; NARC (nucleophilic addition&#8211;ring closure); squalestatin; stereoselective; synthesis; Wacker; zaragozic acid.
%R https://doi.org/10.1071/CH00045
%U https://www.publish.csiro.au/paper/CH00045 
%X A direct method for the preparation of C 5-alkoxycarbonyl-substituted 2,8-dioxabicyclo&#91;3.2.1&#93;octanes is described. The key process involves a highly stereoselective (NARC) sequence of a nucleophilic addition followed by ring closure. 
