Exploration of the biomimetic synthesis of indole-diterpenemycotoxins: an unexpected cascade reaction during the attempted synthesis of emindole SB
Literature Information
J. Stephen Clark, James Myatt, Claire Wilson, Lee Roberts, Nigel Walshe
The key step in an attempted biomimetic synthesis of the indole-diterpene mycotoxin emindole SB delivers the pentacyclic compound resulting from 6-endo cyclisation instead of the product arising by the 5-exo reaction required in the putative biosynthetic pathway.
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![Ethanone, 1-[4-chloro-2-(methylthio)-5-pyrimidinyl]- structure Ethanone, 1-[4-chloro-2-(methylthio)-5-pyrimidinyl]- structure](https://static.chemtradehub.com/structs/661/66116-82-3-863e.webp)



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