A rapid enantiospecific synthesis of the (6,6,5)-tricyclic ring system of the elisabethane diterpenes

@article{Srikrishna2007ARE,
  title={A rapid enantiospecific synthesis of the (6,6,5)-tricyclic ring system of the elisabethane diterpenes},
  author={A. Srikrishna and Vijendra H. Pardeshi and G. Satyanarayana},
  journal={Tetrahedron Letters},
  year={2007},
  volume={48},
  pages={4087-4090}
}
  • A. Srikrishna, Vijendra H. Pardeshi, G. Satyanarayana
  • Published 2007
  • Chemistry
  • Tetrahedron Letters
  • A rapid enantiospecific stereoselective synthesis of the 6,6,5-ring system of the novel tricyclic elisabethin diterpenes, starting from (R)-carvone, employing a ROM-RCM sequence as the key step, has been accomplished. 
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