Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone

@article{Srikrishna2010EnantiospecificFT,
  title={Enantiospecific first total synthesis and confirmation of the relative and absolute stereostructure of isocalamusenone},
  author={A. Srikrishna and Vijendra H. Pardeshi and K. Mahesh},
  journal={Tetrahedron-asymmetry},
  year={2010},
  volume={21},
  pages={2512-2516}
}
  • A. Srikrishna, Vijendra H. Pardeshi, K. Mahesh
  • Published 2010
  • Chemistry
  • Tetrahedron-asymmetry
    • The enantiospecific total synthesis of two epimers of the sesquiterpene isocalamusenone has been accomplished starting from the readily available monoterpene (R)-limonene, which of the natural product established the stereostructure and the absolute configuration. 
    View via Publisher
    4 Citations
    4 Citations
    Citation Type

    Citation Type

    Enantiospecific first total synthesis of (6S,7R)-silphiperfolan-6-ol
    • 5
    Chiral Acylic Synthetic Intermediates from Readily Available Monoterpenoids
    • 2
    The substrate dependent competitive formation of cyclobutanones and cyclopentanones in an intramolecular rhodium carbenoid CH insertion reaction: enantiospecific total synthesis of silphiperfol-6-ene
    • 3
    Identification and Characterization of Biopesticides fromAcorus tatarinowiiandA. calamus

    References

    SHOWING 1-10 OF 13 REFERENCES
    Enantiospecific first total synthesis and assignment of absolute configuration of the sesquiterpene (-)-cucumin H.
    • 31
    Enantiospecific total synthesis of aciphyllene
    • 12
    Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction
    • 13
    A stereoselective total synthesis of (+)-a-herbertenol
    • 11
    An enantiospecific formal total synthesis of (−)-aplysin and (−)-debromoaplysin
    • 25
    Intramolecular Ene Reactions in Organic Synthesis
    • 297
    A Convenient Enantiospecific Methodology for (‐)‐(1R,5S)‐1,5‐Dimethylbicyclo[3.3.0]octa‐2,7‐dione: A Formal Total Synthesis of (‐)‐Ceratopicanol.
    • 3
    • PDF
    Regio- and stereo-selective syntheses of cyclic natural products by intramolecular cycloaddition- and ene-reactions
    • 44
    • PDF
    New sesquiterpenoids of sweet flag oil (Acorus calamus)
    • 18
    Intramolecular Diels-Alder and Alder Ene Reactions
    • 108