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- W2766306160 abstract "A practical and asymmetric synthesis of a functionalized trans-cyclopropoxy building block for the preparation of the HCV NS3/4a protease inhibitor grazoprevir is reported. Intramolecular SN2 displacement–ring closure, followed by a Baeyer–Villiger oxidation, yields the desired trans-cyclopropanol with full control of diastereoselectivity. A terminal alkyne is then effectively installed using LiNH(CH2)2NEt2. Starting from (S)-epichlorohydrin, the cyclopropoxy building block is prepared in 51% overall yield with >99.8% optical purity without isolation of any intermediates." @default.
- W2766306160 created "2017-11-10" @default.
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- W2766306160 date "2017-10-20" @default.
- W2766306160 modified "2023-10-17" @default.
- W2766306160 title "Asymmetric Synthesis of Functionalized <i>trans-</i>Cyclopropoxy Building Block for Grazoprevir" @default.
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- W2766306160 doi "https://doi.org/10.1021/acs.orglett.7b02867" @default.
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