Abstract
We describe herein the ring-opening reaction of chiral 1,1’-sulfonyl bis-aziridines with various neutral and anionic nucleophiles including benzylamine, piperidine, acetate, allylthiolate, cyanide anion and sodium ethoxide. These reactions afforded bis-opened or/and mono-opened compounds via a regioselective attack on the non-substituted methylene of aziridine ring. The structures of the products were confirmed based on spectral analysis (IR, 1H NMR and 13C NMR). A theoretical study by density functional theory (DFT) was used to rationalize the region-selective ring-opening of starting bis-aziridines.
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