A tandem process for the synthesis of β-aminoboronic acids from aziridines with haloamine intermediates
2022
Park, Subin | Koo, Jangwoo | Kim, Weonjeong | Lee, Hong Geun
An unprecedented synthetic strategy is devised to generate β-aminoboronic acids from aziridines via a sequential process involving 1,2-iodoamine formation and radical borylation under light irradiation. A variety of aziridines including multiply substituted aziridines have been successfully employed as synthetic precursors, expanding their synthetic utility compared to previous methods. Mechanistic studies suggest that the boron source plays a unique role in the borylation step, and in the formation of haloamine intermediates.
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Эту запись предоставил National Agricultural Library