Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
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Total Synthesis of Dihydroreynosin and Dihydrosantamarine via Tandem Cope-Claisen Rearrangement

  • Ki-Whan Chi (Department of Chemistry, University of Ulsan) ;
  • Stanley Raucher (Department of Chemistry, University of Washington)
  • Published : 1991.04.20
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Abstract

The total synthesis of dihydroreynosin (1) and dihydrosantamarine (2) via tandem Cope-Claisen rearrangement has been accomplished starting from (S)-carvone (4).

Keywords

References

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Cited by

  1. ChemInform Abstract: Total Synthesis of Dihydroreynosin and Dihydrosantamarine via Tandem Cope-Claisen Rearrangement. vol.22, pp.39, 1991, https://doi.org/10.1002/chin.199139218
  2. Effects of Solvents and Water in Ti(III)-Mediated Radical Cyclizations of Epoxygermacrolides. Straightforward Synthesis and Absolute Stereochemistry of (+)-3&agr;-Hydroxyreynosin and Related Eude vol.67, pp.8, 1991, https://doi.org/10.1021/jo016277e