Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction

@article{Srikrishna2010EnantioselectiveFT,
  title={Enantioselective formal total syntheses of Clavukerin A and isoclavukerin A via a ring-closing metathesis reaction},
  author={A. Srikrishna and Vijendra H. Pardeshi and G. Satyanarayana},
  journal={Tetrahedron-asymmetry},
  year={2010},
  volume={21},
  pages={746-750}
}
  • A. Srikrishna, Vijendra H. Pardeshi, G. Satyanarayana
  • Published 2010
  • Chemistry
  • Tetrahedron-asymmetry
  • Enantioselective formal total syntheses of the marine trisnorsesquiterpenes clavukerin A and isoclavukerin A, starting from (R)-limonene employing an RCM reaction as the key step, are described. 
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