Literature DB >> 35191139

Divergent Total Synthesis of Four Kopsane Alkaloids: N-Carbomethoxy-10,22-dioxokopsane, Epikopsanol-10-lactam, 10,22-Dioxokopsane, and N-Methylkopsanone.

Bo Qin1, Zhepei Lu1, Yanxing Jia1.   

Abstract

We have achieved the divergent total synthesis of four kopsane alkaloids which share a complex heptacyclic caged ring system. Key transformations include an asymmetric Diels-Alder reaction to assemble the central bicyclo[2.2.2]octane moiety and the quaternary stereocenter at C20, a SmI2 -mediated cascade reduction/aldol reaction to construct the five-membered ring and the quaternary stereocenter at C7, and a late-stage cascade reductive amination/cyclization to establish the highly strained caged ring system.
© 2022 Wiley-VCH GmbH.

Entities:  

Keywords:  Cascade Reactions; Diels-Alder Reaction; Indole Alkaloids; Natural Products; Total Synthesis

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Year:  2022        PMID: 35191139     DOI: 10.1002/anie.202201712

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  1 in total

1.  Asymmetric Total Synthesis of (-)-Phaeocaulisin A.

Authors:  Áron Péter; Giacomo E M Crisenza; David J Procter
Journal:  J Am Chem Soc       Date:  2022-04-13       Impact factor: 16.383

  1 in total

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