five

Atropisomerism-Induced Facial Selectivity in Nitrile Oxide Cycloadditions with 5-Methylenehydantoins

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Figshare2016-02-23 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Atropisomerism_Induced_Facial_Selectivity_in_Nitrile_Oxide_Cycloadditions_with_5_Methylenehydantoins/2622118
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资源简介:
N-Aryl 5-methylenehydantoins underwent nitrile oxide cycloaddition with benzonitrile oxide to give 5-spiro isoxazoline adducts with complete regioselectivity. Atropisomerism around the N-aryl bond also led to facial selectivity in these cycloadditions.
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2016-02-23
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