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April 21, 2026The Journal of Organic Chemistry0 citations

A Total Synthesis of (+)-Mitragynine

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DGDnyaneshwar A. GorveGMGour H. MandalKSK. P. Chandra Shekar

Key Points

  • The aim is to achieve a concise total synthesis of (+)-mitragynine from basic commercial materials.
  • Linear synthesis involving seven steps from commercial starting materials
  • Oxidative cyclization as a key reaction in the synthesis
  • Achieved the shortest preparation of (+)-mitragynine to date
  • Demonstrated efficient use of starting materials through a linear sequence

Abstract

Here, we disclose a concise total synthesis of (+)-mitragynine, which is the enantiomer of one of the analgesic components of the Mitragyna speciosa (kratom) plant. The synthesis proceeds in a linear sequence of seven steps from commercial starting materials and constitutes the shortest preparation of (+)-mitragynine to date. An interesting oxidative cyclization contributes to the convergency of the synthesis.

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Cite This Study

Gorve et al. (2026) studied this question.

synapsesocial.com/papers/69e713fdcb99343efc98d72ehttps://doi.org/10.1021/acs.joc.6c00583
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