Diastereoselective [3 + 2] Cycloaddition between Tertiary Amine N -Oxides and Substituted Alkenes to Access 7-Azanorbornanes.
Alexander H CocolasAiden M LaneBenjamin S MusiakEric J ChartierDerek A BedillionSarah L HejnoszJeffrey J RohdePaul A LummisJeffrey D EvanseckThomas D MontgomeryPublished in: Organic letters (2024)
We have developed a diastereoselective synthesis of 43 novel 7-azanorbornanes using tertiary amine N -oxides and substituted alkenes. Our method uses an efficient [3 + 2] cycloaddition, starting from either commercially available or easily accessible precursors to generate yields up to 97% and diastereomeric ratios up to >20:1. Density functional theory (DFT) calculations were performed, suggesting that the observed diastereoselectivity is likely due to steric considerations.