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https://doi.org/10.1016/j.tetlet.2010.05.063
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Cite Journal: Tetrahedron Letters |  Publication Date: May 21, 2010 |
 Citations: 26 |
Affiliation: Indian Institute of Chemical Technology
Abstract The enantioselective total synthesis of (+)-patulolide C isolated from Penicillium urticae has been achieved from commercially available 9-decen-1-ol. Jacobsen’s kinetic resolution and sequential α-aminooxylation and Horner–Wadsworth–Emmons (HWE) olefination followed by Yamaguchi lactonization are used as the key reaction steps.
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