# A Total Synthesis of (−)-Strychnine Using Photoredox Catalysis

**Authors:** Rainer Wiechert, Leander Geske, Jasmin Hammes, Dogus Tuncer, Till Opatz

PMC · DOI: 10.1021/jacsau.5c01709 · 2026-02-23

## TL;DR

The paper presents a new and efficient way to synthesize strychnine using light-driven chemical reactions.

## Contribution

A novel synthesis route for strychnine using photoredox catalysis and renewable starting materials.

## Key findings

- A photoredox-catalytic C2-cyanomethylation step was successfully used.
- A condensation-electrocyclization cascade efficiently linked two fragments.
- Photochemical decarboxylation provided access to strychnofluorine.

## 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.

## Linked entities

- **Chemicals:** strychnine (PubChem CID 441071), Wieland–Gumlich aldehyde (PubChem CID 160466), Boc-l-Trp-OMe (PubChem CID 7021503)

## Full-text entities

- **Chemicals:** Boc-l-Trp-OMe (-), (-)-Strychnine (MESH:D013331)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13014235/full.md

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Source: https://tomesphere.com/paper/PMC13014235