jo101531b_si_005.cif (13.62 kB)
Stereoselective α,α′-Annelation Reactions of 1,3-Dioxan-5-ones
datasetposted on 2010-11-05, 00:00 authored by Tyrone C. Casey, Julie Carlisle, Patrizia Tisselli, Louise Male, Neil Spencer, Richard S. Grainger
Pyrrolidine enamines derived from three 1,3-dioxan-5-ones undergo α,α′-annelation reactions with methyl α-(bromomethyl)acrylate to produce bridged 2,4-dioxabicyclo[3.3.1]nonane ring systems with complete stereocontrol. Stereochemical outcomes have been rationalized based on steric and stereoelectronic interactions in intermediate boat-like conformations of the 1,3-dioxane ring and subsequent kinetic protonation to set an axial ester group on the cyclohexanone ring. Base-mediated ester epimerization provides the stereochemical array found in the highly oxygenated cyclohexane ring of phyllaemblic acid and glochicoccins B and D.