An expeditious route to carbocyclic nucleosides: (-)-Aristeromycin and (-)-carbodine

DOI: 10.1016/S0960-894X(96)00619-1

Source and publish data:

Bioorganic and Medicinal Chemistry Letters p. 247 - 250 (1997)

Update date:2022-07-30

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Authors:

Burlina, Fabienne

Favre, Alain

Fourrey, Jean-Louis

Thomas, Martial

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Article abstract of DOI:10.1016/S0960-894X(96)00619-1

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.

Full text of DOI:10.1016/S0960-894X(96)00619-1

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