All Stories

  1. ChemInform Abstract: Microwave-Assisted Cycloaddition Reactions in Carbo- and Heterocyclic Chemistry
  2. Development of environmentally sensitive fluorescent and dual emissive deoxyuridine analogues
  3. Efficient and selective azidation of per-O-acetylated sugars using ultrasound activation: application to the one-pot synthesis of 1,2,3-triazole glycosides
  4. FeCl3-promoted and ultrasound-assisted synthesis of resveratrol O-derived glycoside analogs
  5. Microwave-assisted Cycloaddition Reactions in Carbo- and Heterocyclic Chemistry
  6. Targeting the Production of Oncogenic MicroRNAs with Multimodal Synthetic Small Molecules
  7. Rational Design of a Solvatochromic Fluorescent Uracil Analogue with a Dual-Band Ratiometric Response Based on 3-Hydroxychromone
  8. Artificial Nucleobase-Amino Acid Conjugates: A New Class of TAR RNA Binding Agents
  9. Can we use the epigenetic bioactivity of caloric restriction and phytochemicals to promote healthy ageing?
  10. Natural Polyphenols as Potent Inhibitors of DNA Methyltransferases
  11. ChemInform Abstract: Sono-Transition-Metal Catalysis of One-Pot Three-Step Synthesis of Glycosyl-1,2,3-triazoles.
  12. ChemInform Abstract: Microwave-Assisted Cycloaddition Reactions
  13. Recent Advances in Drug Design of Epidermal Growth Factor Receptor Inhibitors
  14. Microwave-Assisted Cycloaddition Reactions
  15. Sono-Transition-Metal Catalysis of One-Pot Three-Step Synthesis of Glycosyl-1,2,3-triazoles
  16. Ultrasound-assisted one-pot synthesis of anti-CML nucleosides featuring 1,2,3-triazole nucleobase under iron-copper catalysis
  17. A Universal Nucleoside with Strong Two-Band Switchable Fluorescence and Sensitivity to the Environment for Investigating DNA Interactions
  18. Sequence-Specific Base Pair Mimics Are Efficient Topoisomerase IB Inhibitors
  19. Small molecules DNAmethyltransferasesinhibitors
  20. ChemInform Abstract: A Mild and Efficient Protocol for the Protection of 3-Hydroxychromones under Phase-Transfer Catalysis.
  21. A Mild and Efficient Protocol for the Protection of 3-Hydroxychromones Under Phase-Transfer Catalysis
  22. ChemInform Abstract: Targeting DNA Base Pair Mismatch with Artificial Nucleobases. Advances and Perspectives in Triple Helix Strategy
  23. Targeting DNA base pair mismatch with artificial nucleobases. Advances and perspectives in triple helix strategy
  24. ChemInform Abstract: Syntheses of α-Substituted Cyclohexenones by Thermolysis of Tertiary Ketosulfoxides.
  25. ChemInform Abstract: N-Alkylated Derivatives of 4-Nitroimidazole: Synthesis by Radical Chemistry (SRN1) and Functionalization.
  26. ChemInform Abstract: N-1 Oxidation of Adenine Substituted at N-9 by an Olefinic Chain.
  27. ChemInform Abstract: A Highly Selective and Efficient Access to N-9 Alkylated Purine Derivatives via Radical SRN1 Chemistry.
  28. ChemInform Abstract: N-Alkylated Purine Derivatives. Synthesis by SRN1 Reaction and Transformation of Functional Groups.
  29. ChemInform Abstract: Synthesis of Novel Functionalized Olefins via Fragmentation of SRN1 Products with a Cyclanone β-Ester Subunit.
  30. ChemInform Abstract: New and Straightforward Access to Olefins, Butenolides and β- Nitro γ-Butyrolactones from Precursors Obtained via SRN1 Reactions.
  31. ChemInform Abstract: A Convenient Synthesis of 1-Ethoxymethyl-5-nitro-6-substituted Uracils.
  32. ChemInform Abstract: Synthesis and Anti-HIV Activity of Novel N-1 Side Chain-Modified Analogues of 1-((2-Hydroxyethoxy)methyl)-6-(phenylthio)thymine (HEPT).
  33. ChemInform Abstract: First Total Synthesis of Fungerin an Antifungal Alkaloid from Fusarium sp.
  34. ChemInform Abstract: Incorporation of Serinol-Derived Acyclic Nucleoside Analogues into Oligonucleotides: Influence on Duplex and Triplex Formation.
  35. ChemInform Abstract: A Mild and Effective Iodination Method Using Iodine in the Presence of Bis-(trifluoroacetoxy)iodobenzene.
  36. ChemInform Abstract: Synthesis of 6-Allyl and 6-Heteroarylindoles by Palladium-Catalyzed Stille Cross-Coupling Reaction.
  37. ChemInform Abstract: Efficient Stereoselective Synthesis of New C-Nucleosides via Intramolecular Mitsunobu Cyclization
  38. ChemInform Abstract: Incorporation of a Novel Nucleobase Allows Stable Oligonucleotide-Directed Triple Helix Formation at the Target Sequence Containing a Purine×Pyrimidine Interruption.
  39. ChemInform Abstract: Reactivity of 1,1′-Thiocarbonyldiimidazole with Glycosides: A Novel and Efficient Glycosidic Activation.
  40. ChemInform Abstract: Bicyclic Anti-VZV Nucleosides: Thieno Analogues Retain Full Antiviral Activity.
  41. ChemInform Abstract: Stereocontrolled Synthesis of Heterocyclic C-Nucleosides. Protecting Group Effect and Molecular Modeling Studies.
  42. Microwave-Assisted and Efficient Solvent-free Knoevenagel Condensation. A Sustainable Protocol Using Porous Calcium Hydroxyapatite as Catalyst
  43. Design of novel RNA ligands that bind stem–bulge HIV-1 TAR RNA
  44. ChemInform Abstract: Tandem Azide—Alkyne 1,3-Dipolar Cycloaddition/Electrophilic Addition: A Concise Three-Component Route to 4,5-Disubstituted Triazolyl-Nucleosides.
  45. Efficient Synthesis of Ratiometric Fluorescent Nucleosides Featuring 3-Hydroxychromone Nucleobases
  46. Tandem Azide-Alkyne 1,3-Dipolar Cycloaddition/Electrophilic Addition: A Concise Three-Component Route to 4,5-Disubstituted Triazolyl-Nucleosides
  47. From Intriguing Reactivity of 2-Bromothiophene to the First Synthesis of C1′-Disubstituted C-Nucleosides
  48. A stereo- and regio-controlled synthesis of bromothiophenyl C-nucleosides. Tandem bromination-ribosylation via halogen dance process
  49. Friedel–Crafts and modified Vorbrüggen ribosylation. A short synthesis of aryl and heteroaryl-C-nucleosides
  50. Efficient Synthesis of α- and β-2′-Deoxy-heteroaryl- C -nucleosides
  51. ChemInform Abstract: Efficient Synthesis and in vitro Cytostatic Activity of 4-Substituted Triazolyl-Nucleosides.
  52. Efficient synthesis and in vitro cytostatic activity of 4-substituted triazolyl-nucleosides
  53. An efficient one-step regiospecific synthesis of novel isoxazolines and isoxazoles of N-substituted saccharin derivatives through solvent-free microwave-assisted [3+2] cycloaddition
  54. A Highly Efficient Microwave-Assisted Solvent-Free Synthesis of α- and β-2′-Deoxy-1,2,3-triazolyl-nucleosides.
  55. A highly efficient microwave-assisted solvent-free synthesis of α- and β-2′-deoxy-1,2,3-triazolyl-nucleosides
  56. Synthesis and in vitro antileishmanial activity of 5-substituted-2′-deoxyuridine derivatives
  57. Synthesis of Mono- and Polyhydroxylated Cyclobutane Nucleoside Analogues.
  58. First Example of Base-Promoted Tandem Alkylation—Bromination of 2-Bromothiophene via Halogen Dance Process: A Remarkable Temperature Effect.
  59. Synthesis of mono- and polyhydroxylated cyclobutane nucleoside analogs
  60. The ‘fully protected backbone’ approach as a versatile tool for a new solid-phase PNA synthesis strategy
  61. First example of base-promoted tandem alkylation–bromination of 2-bromothiophene via halogen dance process: a remarkable temperature effect
  62. Ultrasound-Accelerated Aromatization of trans- and cis-Pyrazolines under Heterogeneous Conditions Using Claycop.
  63. Efficient synthesis of extended guanine analogues designed for recognition of an A·T inverted base pair in triple helix based-strategy
  64. Ultrasound-accelerated aromatisation of trans- and cis-pyrazolines under heterogeneous conditions using claycop
  65. Synthesis and Triplex Binding Properties of Oligonucleotides Containing a Novel Nucleobase
  66. Synthesis and Studies of Modified Oligonucleotides-Directed Triple Helix Formation at the Purine-Pyrimidine Interrupted Site
  67. A Short and Efficient Synthesis of 2′-Deoxybenzo- and Pyridoimidazole C-Nucleosides.
  68. Synthesis and Studies of Modified Oligonucleotides- Directed Triple Helix Formation at the Purine-Pyrimidine Interrupted Site
  69. Synthesis and Triplex Binding Properties of Oligonucleotides Containing a Novel Nucleobase
  70. A short and efficient synthesis of 2′-deoxybenzo- and pyridoimidazole C-nucleosides
  71. A Short and Highly Stereoselective Synthesis of α-(2-Aminothiazolyl)-C-nucleosides.
  72. A short and highly stereoselective synthesis of α-(2-aminothiazolyl)-C-nucleosides
  73. A Short Synthesis of Aspergillamide B. The Marine Natural Product from Aspergillus sp.
  74. Synthesis, Incorporation into Triplex-Forming Oligonucleotide, and Binding Properties of a Novel 2‘-Deoxy- C -Nucleoside Featuring a 6-(Thiazolyl-5)benzimidazole Nucleobase
  75. A short synthesis of aspergillamide B. The marine natural product from Aspergillus sp.
  76. Stereocontrolled Synthesis of Heterocyclic C-Nucleosides. Protecting Group Effect and Molecular Modeling Studies
  77. Binding properties of oligonucleotides containing a modified 2′-deoxyuridine with a thymine ended linker to pair with 2′-deoxyadenosine
  78. Reactivity of 1,1′-thiocarbonyldiimidazole with glycosides: a novel and efficient glycosidic activation
  79. Bicyclic anti-VZV nucleosides: Thieno analogues retain full antiviral activity
  80. ChemInform Abstract: Efficient Stereocontrolled Synthesis of 2-Benzimidazolyl- and 2-Indolyl-C-nucleosides.
  81. ChemInform Abstract: DNA Triplex Structures Are Stabilized by the Incorporation of 3′-endo Blocked Pyrimidine Nucleosides in the Hoogsteen Strand.
  82. Incorporation of a novel nucleobase allows stable oligonucleotide-directed triple helix formation at the target sequence containing a purine·pyrimidine interruption
  83. Efficient stereocontrolled synthesis of 2-benzimidazolyl- and 2-indolyl-C-nucleosides
  84. DNA triplex structures are stabilized by the incorporation of 3′-endo blocked pyrimidine nucleosides in the hoogsteen strand
  85. ChemInform Abstract: Selective N-Trifluoroacetylation of ortho-Arylenediamines under Ultrasound
  86. N-Trifluoroacétylation sélective d'ortho-arylènediamines sous ultrasons
  87. NMR recognition studies of C·G base pairs by new easily accessible heterobicyclic systems
  88. Synthesis of 6-allyl and 6-heteroarylindoles by palladium catalyzed Stille cross-coupling reaction
  89. NMR Studies of Triplex Formation - Recognition of C•G Base Pairs by New Heterocyclic Systems
  90. Efficient Stereoselective Synthesis of New C-Nucleosides via Intramolecular Mitsunobu Cyclization
  91. Novel 2′-deoxycytidine analogues as pH independent substitutes of protonated cytosines in triple helix forming oligonucleotides
  92. A mild and effective iodination method using iodine in the presence of bis-(trifluoroacetoxy)iodobenzene
  93. First total synthesis of fungerin an antifungal alkaloid from Fusarium sp.
  94. Incorporation of serinol derived acyclic nucleoside analogues into oligonucleotides: Influence on duplex and triplex formation
  95. Synthesis and Anti-HIV Activity of Novel N-1 Side Chain-Modified Analogs of 1-[(2-Hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT)
  96. A convenient synthesis of 1-ethoxymethyl-5-nitro-6-substituted uracils
  97. Bromoalkoxy Addition on N-Azolyl Olefins
  98. Selective N1-Alkylation of Pyrimidine BasesviaRadical (SRN1) Mechanism
  99. A Highly Selective and Efficient Access to N-9 Alkylated Purine DerivativesviaRadical SRN1 Chemistry
  100. Tetrasubstituted N-Azolyl Olefins via Products from Sequential S RN 1 Reactions
  101. N-1 Oxidation of Adenine Substituted at N-9 by an Olefinic Chain
  102. SYNTHESES DE CYCLOHEXENONES α-SUBSTITUEES VIA LA THERMOLYSE DE CETOSULFOXYDES TERTIAIRES