All Stories

  1. Stabilization of hairpins and bulged secondary structures of nucleic acids by single incorporation of α,β-D-CNA featuring a gauche(+) alpha torsional angle
  2. Pd0-Catalyzed Methyl Transfer on Nucleosides and Oligonucleotides, Envisaged as a PET Tracer
  3. Oligonucleotide Labelling Using a Fluorogenic “Click” Reaction with a Hemicarboxonium Salt
  4. Synthesis of Conformationally Constrained Nucleoside Analogues
  5. Synthesis and Structural Study of ribo‐Dioxaphosphorinane‐Constrained Nucleic Acid Dinucleotides (ribo‐α,β‐D‐CNA)
  6. Synthesis of Phostone‐Constrained Nucleic Acid (P‐CNA) Dinucleotides Through Intramolecular Arbuzov's Reaction
  7. Silicon‐Based Chemistry: An Original and Efficient One‐Step Approach to [18F]‐Nucleosides and [18F]‐Oligonucleotides for PET Imaging
  8. α,β-D-CNA featuring canonical and noncanonical α/β torsional angles behaviours within oligonucleotides
  9. ChemInform Abstract: Synthesis of Bicyclonucleosides Having a C—C Bridge
  10. Synthesis of Bicyclonucleosides Having a C−C Bridge
  11. ChemInform Abstract: Cyclic Phospho Di‐ and Triesters as Structural Elements of Nucleic Acids
  12. α,β-D-CNA preorganization of unpaired loop moiety stabilizes DNA hairpin
  13. Synthesis and luminescence properties of a trinucleotide–europium(III) complex conjugate
  14. ChemInform Abstract: Synthesis of Spiro ε,ζ‐D‐CNA in xylo Configuration Featuring Noncanonical δ/ε/ζ Torsion Angle Combination.
  15. α,β-D-CNA induced rigidity within oligonucleotides
  16. Synthesis of spiro ɛ,ζ-D-CNA in xylo configuration featuring noncanonical δ/ɛ/ζ torsion angle combination
  17. Synthesis and Structure of Dinucleotides Featuring Canonical and Non‐canonical A‐Type Duplex α, β and δ Torsion Angle Combinations (LNA/α,β‐D‐CNA)
  18. Synthesis and Structure of an α,β‐D‐CNA Featuring a Noncanonical α/β Torsion Angle Combination within a Tetranucleotide
  19. Diastereoselective Synthesis of Conformationally Restricted Dinucleotides Featuring Canonical and Noncanonical α/β Torsion Angle Combinations(α,β‐D‐CNA)
  20. Watson–Crick Base‐Pairing Properties of Nucleic Acid Analogues with Stereocontrolled α and β Torsion Angles (α,β‐D‐CNAs)
  21. Watson–Crick Base‐Pairing Properties of Nucleic Acid Analogues with Stereocontrolled α and β Torsion Angles (α,β‐D‐CNAs)
  22. Constrained Nucleic Acids (CNA). Part 2. Synthesis of Conformationally Restricted Dinucleotide Units Featuring Noncanonical α/β/γ or δ/ε/ζ Torsion Angle Combinations
  23. Diastereoselective Synthesis of a Conformationally Restricted Dinucleotide with Predefined α and β Torsional Angles for the Construction of α,β-Constrained Nucleic Acids (α,β-CNA)
  24. Stereoselective Synthesis of (5′S)-5′-C-(5-Bromo-2-penten-1-yl)-2′-deoxyribofuranosyl Thymine, a New Convertible Nucleoside
  25. Stereochemistry Control in the Lewis Acid Mediated Lactonization Reaction of γ,δ-Epoxy-β-silyloxy Esters
  26. ChemInform Abstract: Allylsilanes in the Preparation of 5′‐C‐Hydroxy or Bromo Alkylthymidines.
  27. Allylsilanes in the preparation of 5′-C-hydroxy or bromo alkylthymidines
  28. Total Synthesis of a Thymidine 2-Deoxypolyoxin C Analogue
  29. Influence of the nature and substitution of chiral 2,3‐epoxy alcohol derivatives on the enantiomeric elution order on chiralcel OD column
  30. Stereoselective synthesis of five and/or six membered ring hydroxylactones obtained by Lewis acid mediated reaction of γ,δ-epoxy-β-hydroxyesters; access to 5-methylated 2-deoxysugars.
  31. Synthèse stéréosélective de thymidine substituée en C-5′
  32. Enhanced diastereoselectivity in the addition of ester enolate to optically active α,β-epoxyaldehydes obtained from nerol and geraniol
  33. Synthesis of a 3-Deoxy-D-arabino-2-heptulosonic Acid Derivative
  34. Synthèse de 2′-désoxynucléosides substitués en C-5′
  35. Diastereoface differentiation in addition of lithium enolates to chiral α,β-epoxyaldehydes
  36. A short synthesis of substituted β-hydroxy γ-butyrolactones and 2-deoxyhexofuranosides
  37. Diastereoselection in the addition of enolates to chiral α,β-epoxyaldehydes