1′,2′-Seco-2′-nor-nucleosides carrying a fluorine atom, instead of hydroxyl group, on C-3′ are synthesized in enantiomerically pure form, starting from (2S)-1-fluoro-3-(R)-[(4-methylphenyl)sulfinyl]-2-propanol. The nucleosides , were synthesized in enantiomerically pure form starting from (2S,RS)-.

Optically pure and fluoro substituted acyclovir analogues

BRAVO, PIERFRANCESCO;RESNATI, GIUSEPPE;
1993-01-01

Abstract

1′,2′-Seco-2′-nor-nucleosides carrying a fluorine atom, instead of hydroxyl group, on C-3′ are synthesized in enantiomerically pure form, starting from (2S)-1-fluoro-3-(R)-[(4-methylphenyl)sulfinyl]-2-propanol. The nucleosides , were synthesized in enantiomerically pure form starting from (2S,RS)-.
1993
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/655570
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