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Enantiospecific, biosynthetically inspired formal total synthesis of (+)-liphagal
Jonathan H George1, Jack E Baldwin, Robert M Adlington
1Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford OX1 3TA, UK. jonathan.george@chem.ox.ac.uk
Abstract:
A biosynthetically inspired synthesis of (+)-liphagal has been achieved from (+)-sclareolide in 13 steps (9% overall yield). The key step is a biomimetic ring expansion of a highly stabilized benzylic carbocation, which generates the seven-membered ring and the benzofuran of the natural product in a single cascade reaction.
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