The formal synthesis of (+)-sorangicin A was completed by two independent routes. Both approaches feature a cross metathesis reaction to form the C29-C30 bond to arrive at the bicyclic ether/tetrahydropyran fragment. Formation of the C15-C16 olefin to unite the dihydropyran fragment with the rest of the molecule was achieved by either a cross metathesis reaction or a Julia-Kocienski olefination. © 2011 American Chemical Society.
CITATION STYLE
Crimmins, M. T., Haley, M. W., & O’Bryan, E. A. (2011). Formal synthesis of (+)-sorangicin A. Organic Letters, 13(17), 4712–4715. https://doi.org/10.1021/ol201920j
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