
TY  - JOUR
A1  - Perlmutter, Patrick 
A1  - Selajarern, Walailak 
T1  - 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.
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 2000
VL  - 53
IS  - 4
SP  - 349
EP  - 353
KW  - Aldol; anti-cholesterol; bicyclic acetal; heterocycle; NARC (nucleophilic addition&#8211;ring closure); squalestatin; stereoselective; synthesis; Wacker; zaragozic acid.
UR  - https://doi.org/10.1071/CH00045 
N2  - 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. 
ER  -

