First enantioselective synthesis of methyl (+)-7-methoxyanodendroate, an antitubercular dihydrobenzofuran
Author(s)
Aumann, Kylee M
Hungerford, Natasha L
Coster, Mark J
Year published
2011
Metadata
Show full item recordAbstract
An enantioselective synthesis of methyl (+)-7-methoxyanodendroate was achieved utilising a Claisen rearrangement, a Grubbs cross-metathesis, and a Shi epoxidation-cyclisation sequence, confirming the absolute configuration assigned to the natural product.An enantioselective synthesis of methyl (+)-7-methoxyanodendroate was achieved utilising a Claisen rearrangement, a Grubbs cross-metathesis, and a Shi epoxidation-cyclisation sequence, confirming the absolute configuration assigned to the natural product.
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Journal Title
Tetrahedron Letters
Volume
52
Subject
Medicinal and biomolecular chemistry
Organic chemistry
Organic chemical synthesis