All Stories

  1. Disseminating a Free, Practical Java Tool To Interactively Generate and Edit 2D Chemical Structures
  2. Trehalose 6-phosphate phosphatases of Pseudomonas aeruginosa
  3. Synthesis of spirocyclic orthoesters by ‘anomalous’ rhodium(ii)-catalysed intramolecular C–H insertions
  4. The design, synthesis, and anti-inflammatory evaluation of a drug-like library based on the natural product valerenic acid
  5. Enzyme characteristics of pathogen-specific trehalose-6-phosphate phosphatases
  6. A bidirectional synthesis of spiroacetals via Rh(ii)-catalysed C–H insertion
  7. Dichloro-naphthoquinone as a non-classical inhibitor of the mycobacterial carbonic anhydrase Rv3588c
  8. Probing function and structure of trehalose-6-phosphate phosphatases from pathogenic organisms suggests distinct molecular groupings
  9. Panel docking of small-molecule libraries — Prospects to improve efficiency of lead compound discovery
  10. Synthesis and Antiplasmodial Evaluation of Analogues Based on the Tricyclic Core of Thiaplakortones A–D
  11. Synthesis of N-alkylsulfonamides by borane–dimethyl sulfide reduction of N-acylsulfonamides
  12. Synthesis and antimalarial evaluation of amide and urea derivatives based on the thiaplakortone A natural product scaffold
  13. Rhodium(ii)-catalysed intramolecular C–H insertion α- to oxygen: reactivity, selectivity and applications to natural product synthesis
  14. Total synthesis of (±)-nicolaioidesin B via a highly regio- and diastereoselective Diels–Alder reaction
  15. Total Synthesis of Thiaplakortone A: Derivatives as Metabolically Stable Leads for the Treatment of Malaria
  16. Synthesis and Evaluation of Anticancer Natural Product Analogues Based on Angelmarin: Targeting the Tolerance towards Nutrient Deprivation
  17. 3,4′-Linked bis(piperidines) related to the haliclonacyclamine class of marine alkaloids: synthesis using crossed-aldol chemistry and preliminary biological evaluations
  18. First enantioselective synthesis of methyl (+)-7-methoxyanodendroate, an antitubercular dihydrobenzofuran
  19. Mitochondrially Targeted α-Tocopheryl Succinate Is Antiangiogenic: Potential Benefit Against Tumor Angiogenesis but Caution Against Wound Healing
  20. A Concise Route to Dihydrobenzo[b]furans: Formal Total Synthesis of (+)-Lithospermic Acid
  21. Mitochondrial targeting of α-tocopheryl succinate enhances its pro-apoptotic efficacy: A new paradigm for effective cancer therapy
  22. Arylation of [6,6]-spiroacetal enol ethers: reactivity and rearrangement
  23. Mitochondrial Targeting of Vitamin E Succinate Enhances Its Pro-apoptotic and Anti-cancer Activity via Mitochondrial Complex II
  24. Targeting the Resistance of Pancreatic Cancer Cells to Nutrient Deprivation: Anti-Austerity Compounds
  25. Oxo-bridged isomers of aza-trishomocubane sigma (σ) receptor ligands: Synthesis, in vitro binding, and molecular modeling
  26. Total Synthesis of (+)-Angelmarin
  27. Purinergic P2X7 receptor antagonists: Chemistry and fundamentals of biological screening
  28. Behavioural effects of a selective NMDA NR1A/2B receptor antagonist in rats with unilateral 6-OHDA+parafascicular lesions
  29. Evaluation of behavioural effects of a selective NMDA NR1A/2B receptor antagonist in the unilateral 6-OHDA lesion rat model
  30. Cubyl amides: Novel P2X7 receptor antagonists
  31. Synthesis and In-Vivo Evaluation of [11C]p-PVP-MEMA as a PET Radioligand for Imaging Nicotinic Receptors
  32. Asymmetric aldol reaction using boron enolates
  33. Trishomocubanes: Novel σ ligands modulate cocaine-induced behavioural effects
  34. Reversibility in the boron-mediated ketone–ketone aldol reaction
  35. (1R,2S,3R,6S,7R,8S)-Tricyclo[6.2.1.02,7]undeca-4,9-diene-3,6-diol
  36. Total Synthesis of Spongistatin 1 (Altohyrtin A): A Tale of Ten Aldols
  37. The boron-mediated ketone–ketone aldol reaction
  38. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the CD-spiroacetal segment
  39. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: the AB-spiroacetal segment
  40. The stereocontrolled total synthesis of altohyrtin A/spongistatin 1: fragment couplings, completion of the synthesis, analogue generation and biological evaluation
  41. Synthesis and biological evaluation of spongistatin/altohyrtin analogues: E-ring dehydration and C46 side-chain truncationElectronic supplementary information (ESI) available: spectroscopic data for compounds 2 and 3. See http://www.rsc.org/suppdata/cc...
  42. A Total Synthesis of the Styryllactone (+)-Goniodiol from Naphthalene
  43. CP-225,917 and CP-263,114 Synthesis Support Studies: Testing a Radical Cyclization Strategy for Installation of the Side-Chains
  44. Selective Cleavage ofN-Benzyl-Protected Secondary Amines by Triphosgene
  45. Medium Ring Ethers by Ring Expansion−Ring Contraction:  Synthesis of Lauthisan
  46. A chemoenzymatic synthesis of the styryllactone (+)-goniodiol from naphthalene
  47. Stereocontrolled Total Synthesis of (+)-Altohyrtin A/Spongistatin 1 Financial support was provided by the EPSRC (GR/L41646), Cambridge Commonwealth Trust (Scholarship to M.J.C.), EC (Marie Curie Postdoctoral Fellowship to J.L.A.), DFG (Postdoctoral Fel...