This study demonstrates a photocatalytic cycloaddition to produce chiral imidazolidines and 1,2-diamines, suggesting efficient reactions.
This study introduces the first example of a photocatalytic [3 + 2] cycloaddition reaction to efficiently generate novel chiral imidazolidines using a chiral sulfinamide. A broad range of substrates, including different (S)-N-tert-butanesulfinyl imines and dipole precursors, were found to be compatible, delivering chiral imidazolidines in good yields with high diastereoselectivity (up to 93% yield, up to >25:1 dr). The reaction mechanism was investigated through radical trapping experiments. Furthermore, chiral 1,2-diamines were efficiently obtained with excellent enantioselectivities (up to 100:0 er).
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Qin et al. (2025) studied this question.
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