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- W4252847994 endingPage "14025" @default.
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- W4252847994 abstract "Abstract The first total synthesis of the 2,3,5‐ O ‐( S , R )‐nonahydroxytriphenoylated (NHTP) C ‐glucosidic ellagitannin (−)‐vescalin was accomplished through a series of transformations mimicking the sequence of events leading to its biogenesis. The key steps of this synthesis encompass a Wittig‐mediated ring opening of a glucopyranosic hemiacetal, a C‐glucosidation event through a phenolic aldol‐type reaction, and a Wynberg–Feringa–Yamada‐type oxidative phenolic coupling, which forged the NHTP unit of (−)‐vescalin." @default.
- W4252847994 created "2022-05-12" @default.
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- W4252847994 date "2017-09-27" @default.
- W4252847994 modified "2023-10-13" @default.
- W4252847994 title "Bioinspired Total Synthesis of (−)-Vescalin: A Nonahydroxytriphenoylated<i>C</i>-Glucosidic Ellagitannin" @default.
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- W4252847994 doi "https://doi.org/10.1002/ange.201707613" @default.
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