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- W4256405997 abstract "Spiroacetals can be formed through a one-pot sequence of a hetero-Diels–Alder reaction, an oxidative carbon–hydrogen bond cleavage, and an acid treatment. This convergent approach expedites access to a complex molecular subunit which is present in numerous biologically active structures. The utility of the protocol is demonstrated through its application to a brief synthesis of the actin-binding cytotoxin bistramide A." @default.
- W4256405997 created "2022-05-12" @default.
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- W4256405997 date "2014-09-01" @default.
- W4256405997 modified "2023-10-18" @default.
- W4256405997 title "Spiroacetal Formation through Telescoped Cycloaddition and Carbon-Hydrogen Bond Functionalization: Total Synthesis of Bistramide A" @default.
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- W4256405997 doi "https://doi.org/10.1002/ange.201406819" @default.
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