Stereoselective Synthesis of Alfa-5-halo-2’-deoxyuridines

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Sammanfattning

Reversed stereoselectivity is observed, when 5-halouracils are used in place of uracil or thymine in gly-cosidation with 2-deoxy-D-ribose having a β/α-directing 3-O-protection. Several 5-halo-2’-deoxyuridine deriva-tives have been synthesized and the effects on the β/α-ratio are analysed.
Bidragets översatta titelAlfa-5-halo-2'-deoksiuridiinien stereoselektiivinen synteesi
Originalspråkengelska
Titel på värdpublikationXX International Round Table on Nucleosides, Nucleotides & Nucleic Acids
Antal sidor1
Utgivningsdatum2012
StatusPublicerad - 2012
MoE-publikationstypB3 Ej refererad artikel i konferenshandlingar
EvenemangInternational Round Table - Montréal, Kanada
Varaktighet: 5 aug. 20129 aug. 2012
Konferensnummer: 20

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