Frank D. Ferrari, Adele E. Pasqua, Andrew J. Ledgard and Rodolfo Marquez
Org. Biomol. Chem., 2013,11, 3469-3476
DOI:
10.1039/C3OB40284C,
Paper
The enantioselective synthesis of the oxa-pinnaic acid framework has been achieved through internal asymmetric induction. The synthetic strategy pursued illustrates the adaptability of the Achmatowicz oxidative rearrangement for the synthesis of complex spirocyclic pyrans starting from tertiary alcohols.
