(Q62606260)

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Generation of C-1′ radicals through a β-(acyloxy)alkyl rearrangement in modified purine and pyrimidine nucleosides

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Generation of C-1′ radicals through a β-(acyloxy)alkyl rearrangement in modified purine and pyrimidine nucleosides (English)

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Thanasis Gimisis

1

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Chryssostomos Chatgilialoglu

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Chryssostomos Chatgilialoglu

series ordinal

3

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author name string

Giuseppina Ialongo

series ordinal

2

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publication date

January 1998

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published in

Tetrahedron

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volume

54

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issue

3-4

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page(s)

573-592

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cites work

1,5-Radical Translocation Protocol for the Generation of C-1‘ Radicals in Nucleosides. Synthesis of Spiro Nucleosides through a Rare 5-endo-trigCyclization

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A new class of anomeric spironucleosides

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L-thymidine is phosphorylated by herpes simplex virus type 1 thymidine kinase and inhibits viral growth.

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Synthesis and antiviral activity of certain 5'-monophosphates of 9-D-arabinofuranosyladenine and 9-D-arabinofuranosylhypoxanthine

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Rate Constants and Arrhenius Parameters for the Reaction of Acyl Radicals with Bu3SnH and (Me3Si)3SiH

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Rate constants and Arrhenius parameters for the reactions of primary, secondary, and tertiary alkyl radicals with tri-n-butyltin hydride

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A novel method for the synthesis of purine alpha-ribonucleosides

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10.1016/S0040-4020(97)10317-9

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(Q62606260)

Generation of C-1′ radicals through a β-(acyloxy)alkyl rearrangement in modified purine and pyrimidine nucleosides

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