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} }
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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