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Total synthesis of (+)-angelmarin
1Eskitis Institute for Cell and Molecular Therapies, Griffith University, Nathan 4111, Queensland, Australia.
The Journal of Organic Chemistry
|May 23, 2009
Abstract:
An efficient 8-step enantioselective total synthesis of (+)-angelmarin, starting from commercially available umbelliferone, has been achieved. Key reactions include olefin cross-metathesis and a Shi epoxidation-cyclization sequence.
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