Achiral auxiliary-assisted chiral transfer via microwave-accelerated aza-Claisen rearrangement: A short synthesis of (+)-1-hydroxyquinolizidinone

Jaehoon Sim, Hwayoung Yun, Jong Wha Jung, Sujin Lee, Nam Jung Kim, Young Ger Suh

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

A short and efficient synthesis of (+)-1-hydroxyquinolizidinone as an advanced core intermediate for the syntheses of (+)-epiquinamide, (+)-homopumiliotoxin, and (+)-lupinine is described. The key feature of our strategy includes a sequential chiral transfer using an achiral phenylsulfide auxiliary via microwave-accelerated aza-Claisen rearrangement of the unexplored N-thiophenoxyacetyl-α-vinyl piperidine substrate and the oxone-induced transannulation.

Original languageEnglish
Pages (from-to)4813-4815
Number of pages3
JournalTetrahedron Letters
Volume53
Issue number36
DOIs
StatePublished - 5 Sep 2012

Keywords

  • (+)-1-Hydroxyquinolizidinone
  • Achiral auxiliary
  • aza-Claisen rearrangement
  • Quinolizidine alkaloid
  • Transannulation

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