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- W4375857426 abstract "The asymmetric total synthesis of vinorine, a polycyclic and cage-like alkaloid, has been realized in a flexible approach. Key features of the current synthesis include an aza-Achmatowicz rearrangement/Mannich-type cyclization to install the highly functional 9-azabicyclo-[3.3.1]nonane scaffold, a high yield Fischer indole annulation to synthesize the common intermediate for sarpagine-ajamaline type alkaloids, and an Ireland–Claisen rearrangement to construct the C15–C20 bond." @default.
- W4375857426 created "2023-05-10" @default.
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- W4375857426 date "2023-05-08" @default.
- W4375857426 modified "2023-10-18" @default.
- W4375857426 title "Total Synthesis of Vinorine" @default.
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- W4375857426 doi "https://doi.org/10.1021/acs.orglett.3c01041" @default.
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