All Stories

  1. Repurposing HIV-Protease Inhibitor Precursors as Anticancer Agents: The Synthetic Molecule RDD-142 Delays Cell Cycle Progression and Induces Autophagy in HepG2 Cells with Enhanced Efficacy via Liposomal Formulation
  2. From insect lipids to biodiesel through the bioconversion process of vegetable by-products
  3. Recent Advances in Heterocyclic HIV Protease Inhibitors
  4. NCS-Mediated Ipso-Halogenation of Arylboronic Acids in Water Using Sodium Halides
  5. N‐Iodosuccinimide in Oxidative Dimerization of Methyl Cinnamates
  6. Unveiling the Relationship between Structure and Anticancer Properties of Permethylated Anigopreissin A: A Study with Thirteen Analogues
  7. Targeting Viral and Cellular Cysteine Proteases for Treatment of New Variants of SARS-CoV-2
  8. Novel wild type and mutate HIV-1 protease inhibitors containing heteroaryl carboxamides in P2: Synthesis, biological evaluations and in silico ADME prediction
  9. Reactivity Insights of Methoxyphenyl Boronic Acids in Rieche Formylation Reaction
  10. Novel Wild Type and Mutate HIV-1 Protease Inhibitors Containing Heteroaryl Carboxamides in P2: Synthesis, Biological and ADME Evaluations
  11. PEGylated Liposomes Loaded with Carbamate Inhibitor ANP0903 Trigger Apoptosis by Enhancing ER Stress in HepG2 Cancer Cells
  12. Mitochondria-Mediated Apoptosis of HCC Cells Triggered by Knockdown of Glutamate Dehydrogenase 1: Perspective for Its Inhibition through Quercetin and Permethylated Anigopreissin A
  13. Two Novel Precursors of the HIV-1 Protease Inhibitor Darunavir Target the UPR/Proteasome System in Human Hepatocellular Carcinoma Cell Line HepG2
  14. The Pseudo-Symmetric N-benzyl Hydroxyethylamine Core in a New Series of Heteroarylcarboxyamide HIV-1 Pr Inhibitors: Synthesis, Molecular Modeling and Biological Evaluation
  15. The Pseudo-Symmetric N-benzyl Hydroxyethylamine Core in a New Series of Heteroarylcarboxyamide HIV-1 Pr Inhibitors: Synthesis, Molecular Modeling and Biological Evaluation
  16. Regio‐ and Diastereo‐Selective Biomimetic Synthesis of (±)‐ ϵ ‐Viniferin by NIS and Resveratrol
  17. Biginelli Reaction and β-Secretase Inhibition: A Multicomponent Reaction as a Friendly Educational Approach to Bioactive Compounds
  18. Access to 12-Membered Cyclic ortho,meta-Diarylheptanoids: Total Synthesis of Actinidione via Isomyricanone
  19. Structural Insights into the TES/TFA Reduction of Differently Substituted Benzofurans: Dihydrobenzofurans or Bibenzyls?
  20. New synthesized polyoxygenated diarylheptanoids suppress lipopolysaccharide-induced neuroinflammation
  21. New Insights into the Exploitation of Vitis vinifera L. cv. Aglianico Leaf Extracts for Nutraceutical Purposes
  22. Last Decade of Unconventional Methodologies for the Synthesis of Substituted Benzofurans
  23. Recent Advances in Synthetic Strategies to 2,3-Dihydrobenzofurans
  24. Phytochemicals of Minthostachys diffusa Epling and Their Health-Promoting Bioactivities
  25. Green Chemistry, Circular Economy and Sustainable Development: An Operational Perspective to Scale Research Results in SMEs Practices
  26. Unintended Formation of a 26-Membered Cycle in the Course of a Novel Approach to Myricanol, a Strained [7,0]-Metacyclophane
  27. Antioxidant, Antidiabetic, and Anticholinesterase Activities and Phytochemical Profile of Azorella glabra Wedd
  28. Regio- and Diastereoselective Organo-Zinc-Promoted Arylation oftrans-2,3-Diaryloxiranes by Arylboronic Acids: Stereoselective Access totrans-2,3-Diphenyl-2,3-dihydrobenzofuran
  29. New heteroaryl carbamates: Synthesis and biological screening in vitro and in mammalian cells of wild-type and mutant HIV-protease inhibitors
  30. Future in the Past: Azorella glabra Wedd. as a Source of New Natural Compounds with Antiproliferative and Cytotoxic Activity on Multiple Myeloma Cells
  31. Antioxidant Activity and Phytochemical Characterization of Senecio clivicolus Wedd.
  32. Mussel-Inspired Electro-Cross-Linking of Enzymes for the Development of Biosensors
  33. Convergent total synthesis of (±) myricanol, a cyclic natural diarylheptanoid
  34. First application of homogeneous Pd nanoparticles prepared by pulsed laser ablation in liquid to a Suzuki-type reaction
  35. Synthesis and biological evaluation in vitro and in mammalian cells of new heteroaryl carboxyamides as HIV-protease inhibitors
  36. Selective Claisen rearrangement and iodination for the synthesis of polyoxygenated allyl phenol derivatives
  37. A mild access to chiral syn 1,2-diaryl glycols by stereoselective ring opening of ortho substituted trans 2,3-diaryl-oxiranes using Amberlyst 15 in H2O/THF system
  38. Permethylated Anigopreissin A inhibits human hepatoma cell proliferation by mitochondria-induced apoptosis
  39. Nickel-Catalyzed C-Br/C-H Bis-phenylation of Methyl 4-Bromocrotonate: A Stereoselective Entry to Methyl (E)-3,4-Diphenylbut-2-enoate
  40. Practical and efficient ipso-iodination of arylboronic acids via KF/I2 system
  41. Synthesis and biological evaluation of new simple indolic non peptidic HIV Protease inhibitors: The effect of different substitution patterns
  42. Ligand-Free Suzuki Coupling of Arylboronic Acids with Methyl (E)-4-Bromobut-2-enoate: Synthesis of Unconventional Cores of HIV-1 Protease Inhibitors
  43. Synthesis and biological evaluation of novel small non-peptidic HIV-1 PIs: The benzothiophene ring as an effective moiety
  44. Heterocycles in Peptidomimetics and Pseudopeptides: Design and Synthesis
  45. Stereoselective intramolecular cyclization to 4-(hydroxymethyl)-3-(1H-indolyl)oxazolidin-2-ones
  46. Concise Total Synthesis of Permethylated Anigopreissin A, a New Benzofuryl Resveratrol Dimer
  47. Efficient synthesis of 5-nitro-benzo[b]furans via 2-bromo-4-nitro-phenyl acetates
  48. Synthesis of New Thienyl Ring Containing HIV-1 Protease Inhibitors: Promising Preliminary Pharmacological Evaluation against Recombinant HIV-1 Proteases
  49. New indolic non-peptidic HIV protease inhibitors from (S)-glycidol: synthesis and preliminary biological activity
  50. A first convergent synthesis of the polyolic fragment of the antifungal pentaene macrolide strevertene A
  51. Stereoselective synthesis of versatile 2-chloromercurium-3,5-syn-dihydroxy esters via intramolecular oxymercuration
  52. A Chemical/Computational Approach to the Determination of Absolute Configuration of Flexible and Transparent Molecules: Aliphatic Diols As a Case Study
  53. Novel Chiral Calix[4]arenes by Direct Asymmetric Epoxidation Reaction
  54. Application of Sharpless asymmetric dihydroxylation to thienyl- and benzothienyl acrylates and crotonates
  55. A Concise and Efficient Stereoselective Synthesis of the C1-C11 Fragment of Macrolactin A
  56. Direct Preparation of Z-1,3-Enyne Systems with a TMS-Propargylic Sulfone: Application of a One-Pot Julia Olefination
  57. New Functionalised Hydroxymethyl Ketones from the Mild and Chemoselective KMnO4 Oxidation of Chiral Terminal Olefins
  58. Synthesis, biological activity and modelling studies of two novel anti HIV PR inhibitors with a thiophene containing hydroxyethylamino core
  59. One-Pot Practical Preparation of Novel Propargylic Aryl and Heteroaryl Sulfides and Sulfones
  60. Convergent Highly Stereoselective Preparation of the C12−C24 Fragment of Macrolactin A
  61. A convergent preparation of the C1–C13 fragment of amphotericin B from a single chiral precursor
  62. Synthesis of a first thiophene containing analog of the HIV protease inhibitor nelfinavir
  63. A general protocol for the regio high yielding opening of different glycidol derivatives
  64. Stereoselective synthesis of C15C24 and C25C30 fragments of dolabelides
  65. Preparation of chiral 1,3 skipped anti- and syn-tetrols via highly enantioselective biocatalytic resolution
  66. N-(3-Benzo[b]thienyl)iminophosphoranes toward the Synthesis of Benzo[b]thieno[3,2-b]pyridines: Reactivity and Alternative Regioselectivity with α,β-unsaturated Ketones and Aldehydes
  67. First Stereocontrolled Synthesis of the (3S,5R,7R,10R,11R)-C1−C13 Fragment of Nystatin A1
  68. Chiral polypropionate subunit by a chemoenzymatic approach
  69. First enantioselective synthesis of (-)-seiridin the major phytotoxic metabolite of Seiridium species pathogenic for cypress
  70. Ring opening of 2,3-epoxy 1-tosylates to halohydrins and subsequent elaboration to asymmetrical alcohols