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Synthesis of partially-deuterated 2 '-deoxyribonucleoside blocks and their incorporation into an oligo-DNA for simplification of overcrowding and selective enhancement of resolution and sensitivity in the H-1-NMR spectra
Uppsala University.
Uppsala University.
Uppsala University.
Uppsala University.
1998 (English)In: TETRAHEDRON, ISSN 0040-4020, Vol. 54, no 48, 14487-14514 p.Article in journal (Other scientific) Published
Abstract [en]

The chemical synthesis of appropriately protected partially-deuterated 2'((R) under bar/(S) under bar), 3',5'((R) under bar/(S) under bar)-H-2(3)-2'-deoxyribonucleoside blocks [similar to 43 atom % H-2 at C5'((R) under bar), similar to 57 atom % H-2 at C5

Place, publisher, year, edition, pages
PERGAMON-ELSEVIER SCIENCE LTD , 1998. Vol. 54, no 48, 14487-14514 p.
Keyword [en]
ACID RELATED-COMPOUNDS; NUCLEAR-MAGNETIC-RESONANCE; NMR-WINDOW; METHYLENE PROTONS; GENERAL-SYNTHESIS; CHEMICAL-SHIFTS; RNA; CONFORMATION; RIBONUCLEOSIDES; DERIVATIVES
Identifiers
URN: urn:nbn:se:uu:diva-27421OAI: oai:DiVA.org:uu-27421DiVA: diva2:55316
Note
Addresses: Foldesi A, Univ Uppsala, Ctr Biomed, Dept Bioorgan Chem, Box 581, S-75123 Uppsala, Sweden. Univ Uppsala, Ctr Biomed, Dept Bioorgan Chem, S-75123 Uppsala, Sweden. Lajos Kossuth Univ, Dept Organ Chem, H-4010 Debrecen, Hungary.Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-14

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