Bioorganic and Medicinal Chemistry Letters p. 247 - 250 (1997)
Update date:2022-07-30
Topics:
Burlina, Fabienne
Favre, Alain
Fourrey, Jean-Louis
Thomas, Martial
The readily available bicyclic lactone (-)-1 was transformed into diacetate (-)-2 which served in an expeditious route to (-)-aristeromycin (3a) and (-)-carbodine (3b) in acceptable yields.
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