A total synthesis of (−)-strychnine using photoredox catalysis

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Description of rights: CC-BY-4.0
Item type: Item , ZeitschriftenaufsatzAccess status: Open Access ,

Abstract

A concise route toward (−)-strychnine is presented. Key steps include the photoredox-catalytic C2-cyanomethylation of Boc-l-Trp-OMe and a condensation-electrocyclization cascade linking two fragments convergently to obtain an advanced intermediate. A photochemical decarboxylation provided convenient access to strychnofluorine, which could be transformed through the Wieland–Gumlich aldehyde to strychnine. All building blocks can be traced back to renewable sources.

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JACS Au : an open access journal of the American Chemical Society, 6, 3, ACS, Washington, DC, 2026, https://doi.org/10.1021/jacsau.5c01709

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