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

Research output: Chapter in Book/Report/Conference proceedingConference contributionScientific

Abstract

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.
Translated title of the contributionAlfa-5-halo-2'-deoksiuridiinien stereoselektiivinen synteesi
Original languageEnglish
Title of host publicationXX International Round Table on Nucleosides, Nucleotides & Nucleic Acids
Number of pages1
Publication date2012
Publication statusPublished - 2012
MoE publication typeB3 Article in conference proceedings
EventInternational Round Table - Montréal, Canada
Duration: 5 Aug 20129 Aug 2012
Conference number: 20

Fields of Science

  • 116 Chemical sciences

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