35167-37-4Relevant academic research and scientific papers
Convenient access to 5-membered cyclic iminium ions: Evidence for a stepwise [4 + 2] cycloaddition mechanism
Freeman, Jared L.,Brimble, Margaret A.,Furkert, Daniel P.
, p. 2705 - 2714 (2019/03/13)
In situ generation and reaction of novel 5-membered N-tosyl cyclic α,β-unsaturated iminium ions from readily prepared stable precursors is demonstrated. Formal iminium Diels-Alder cycloaddition proceeded in good yield via a stepwise rather than concerted cycloaddition process, confirmed through the isolation of a Mukaiyama-Michael type intermediate. Relative stereochemistry was determined upon subsequent intramolecular cyclisation under Lewis acid catalysis to afford formal endo 5,6-spirobicyclic adducts, as confirmed by crystallography. Further synthetic elaboration towards complex molecular scaffolds based on the dinoflagellate metabolite portimine, a potent apoptosis inducer, were also developed.
