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ChemInform Abstract: New Fluorinated Nucleoside Analogues with 2-Butenolide Rings Prepared by Nucleophilic Vinylic Fluorine Displacement in 4,4-Dialkyl-2,3-difluorobut-2-en-4-olides.

✍ Scribed by Oldrich Paleta; Zdenek Duda; Antonin Holy

Publisher: John Wiley and Sons
Year: 2010
Weight: 32 KB
Volume: 32
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200128216

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📜 SIMILAR VOLUMES

ChemInform Abstract: Fluorine-Containing

ChemInform Abstract: Fluorine-Containing Butanolides and Butenolides. Vinylic Fluorine Displacement in 4,4-Dialkyl-2,3-difluoro-2-buten-4-olides and a Novel Rearrangement Induced by Organolithium Addition to a Carbonyl Group.

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ChemInform Abstract: Fluorinated Butanol

ChemInform Abstract: Fluorinated Butanolides and Butenolides. Part 5. Synthesis and Nucleophilic Reactions of 3-Chloro-2-fluoro-2-buten-4-olide (IX) as Tetronic Acid Analogue. Conjugate Addition of Hard Nucleophiles and Vinylic Halogen Displacement with Soft Phosphorus Nucleophiles.

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