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 contribution | Alfa-5-halo-2'-deoksiuridiinien stereoselektiivinen synteesi |
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Original language | English |
Title of host publication | XX International Round Table on Nucleosides, Nucleotides & Nucleic Acids |
Number of pages | 1 |
Publication date | 2012 |
Publication status | Published - 2012 |
MoE publication type | B3 Article in conference proceedings |
Event | International Round Table - Montréal, Canada Duration: 5 Aug 2012 → 9 Aug 2012 Conference number: 20 |
Fields of Science
- 116 Chemical sciences