Total Syntheses of (-)-Strictosidine and Related Indole Alkaloid Glycosides

Angew Chem Int Ed Engl. 2020 Aug 3;59(32):13414-13422. doi: 10.1002/anie.202005748. Epub 2020 Jun 3.

Abstract

A collective synthesis of glycosylated monoterpenoid indole alkaloids is reported. A highly diastereoselective Pictet-Spengler reaction with α-cyanotryptamine and secologanin tetraacetate as substrates, followed by a reductive decyanation reaction, was developed for the synthesis of (-)-strictosidine, which is an important intermediate in biosynthesis. This two-step chemical method was established as an alternative to the biosynthetically employed strictosidine synthase. Furthermore, after carrying out chemical and computational studies, a transition state for induction of diastereoselectivity in our newly discovered Pictet-Spengler reaction is proposed. Having achieved the first enantioselective total synthesis of (-)-strictosidine in just 10 steps, subsequent bioinspired transformations resulted in the concise total syntheses of (-)-strictosamide, (-)-neonaucleoside A, (-)-cymoside, and (-)-3α-dihydrocadambine.

Keywords: Pictet-Spengler reaction; monoterpenoid indole alkaloid; strictosidine; synthetic methods; total synthesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Oxidation-Reduction
  • Secologanin Tryptamine Alkaloids / chemical synthesis*
  • Stereoisomerism

Substances

  • Secologanin Tryptamine Alkaloids