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Isothiourea-Mediated Asymmetric Functionalization of 3‑Alkenoic Acids

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https://figshare.com/articles/dataset/Isothiourea_Mediated_Asymmetric_Functionalization_of_3_Alkenoic_Acids/2321179
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Isothiourea HBTM-2.1 promotes the catalytic asymmetric α-functionalization of 3-alkenoic acids through formal [2 + 2] cycloadditions with N-tosyl aldimines and formal [4 + 2] cycloadditions with either 4-aryltrifluoromethyl enones or N-aryl-N-aroyl diazenes, providing useful synthetic building blocks in good yield and with excellent enantiocontrol (up to >99% ee). Stereodefined products are amenable to further synthetic elaboration through manipulation of the olefinic functionality.
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2016-02-18
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