Synthesis and stereochemical characterization of diastereomeric nucleoside-phosphorothioselenoates by NMR methods

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Synthesis and stereochemical characterization of enantiomerically pure nucleoside-phosphorothioselenoates are reported. The effects of solvent and temperature on the vicinal carbon-phosphorus couplings are described and the results are interpreted in terms of conformational changes influenced by stacking interactions between the bases and the phenyl rings.

Original languageEnglish
Pages (from-to)1615-1623
Number of pages9
JournalNucleosides, Nucleotides and Nucleic Acids
Volume20
Issue number9
DOIs
Publication statusPublished - 2001

Fingerprint

Nucleosides
Phosphorus
Carbon
Nuclear magnetic resonance
Temperature

ASJC Scopus subject areas

  • Genetics
  • Biochemistry

Cite this

@article{256b82ab0e634ad89db45e4c842ba1f8,
title = "Synthesis and stereochemical characterization of diastereomeric nucleoside-phosphorothioselenoates by NMR methods",
abstract = "Synthesis and stereochemical characterization of enantiomerically pure nucleoside-phosphorothioselenoates are reported. The effects of solvent and temperature on the vicinal carbon-phosphorus couplings are described and the results are interpreted in terms of conformational changes influenced by stacking interactions between the bases and the phenyl rings.",
author = "M. Kajt{\'a}r-Peredy and I. T{\"o}m{\"o}sk{\"o}zi and E. G{\'a}cs-Baitz",
year = "2001",
doi = "10.1081/NCN-100105899",
language = "English",
volume = "20",
pages = "1615--1623",
journal = "Nucleosides and Nucleotides",
issn = "0732-8311",
publisher = "Taylor and Francis Ltd.",
number = "9",

}

TY - JOUR

T1 - Synthesis and stereochemical characterization of diastereomeric nucleoside-phosphorothioselenoates by NMR methods

AU - Kajtár-Peredy, M.

AU - Tömösközi, I.

AU - Gács-Baitz, E.

PY - 2001

Y1 - 2001

N2 - Synthesis and stereochemical characterization of enantiomerically pure nucleoside-phosphorothioselenoates are reported. The effects of solvent and temperature on the vicinal carbon-phosphorus couplings are described and the results are interpreted in terms of conformational changes influenced by stacking interactions between the bases and the phenyl rings.

AB - Synthesis and stereochemical characterization of enantiomerically pure nucleoside-phosphorothioselenoates are reported. The effects of solvent and temperature on the vicinal carbon-phosphorus couplings are described and the results are interpreted in terms of conformational changes influenced by stacking interactions between the bases and the phenyl rings.

UR - http://www.scopus.com/inward/record.url?scp=0034828145&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0034828145&partnerID=8YFLogxK

U2 - 10.1081/NCN-100105899

DO - 10.1081/NCN-100105899

M3 - Article

C2 - 11580189

AN - SCOPUS:0034828145

VL - 20

SP - 1615

EP - 1623

JO - Nucleosides and Nucleotides

JF - Nucleosides and Nucleotides

SN - 0732-8311

IS - 9

ER -