All Stories

  1. Gas solubility in ionic liquids
  2. New descriptors for gas solubility modelling
  3. Design of sustainable and efficient ILs
  4. Modeling from Theory and Modeling from Data: Complementary or Alternative Approaches? The Case of Ionic Liquids
  5. Polarity study of ionic liquids with the solvatochromic dye Nile Red: a QSPR approach using in silico VolSurf+ descriptors
  6. Cyto- and enzyme toxicities of ionic liquids modelled on the basis of VolSurf+ descriptors and their principal properties
  7. Modelling the aquatic toxicity of ionic liquids by means of VolSurfin silicodescriptors
  8. Prediction of ionic liquid's heat capacity by means of their in silico principal properties
  9. A QSPR approach to the ecotoxicity of ionic liquids (Vibrio fischeri) using VolSurf principal properties
  10. Metal-free synthesis of bisthiophene-core donor acceptor organic photosensitizers for dye-sensitized solar cells
  11. New potent antibacterials against Gram-positive multiresistant pathogens: Effects of side chain modification and chirality in linezolid-like 1,2,4-oxadiazoles
  12. Determination of ionic liquids toxicity scores
  13. New antibacterial linezolid-like 1,2,4-oxadiazoles
  14. A Fluorescent new probe for detecting prefibrillar oligomers in protein misfolding diseases
  15. New heteroaryl ethylenes active "in vitro" against MCF-7 breast cancer cell-line
  16. Design, synthesis and in vitro antitumour activity of new heteroaryl ethylenes
  17. NLO properties of new trans 2-(thiophen-2-yl)vinyl heteroaromatic iodides
  18. OPLS-DA as a Suitable Method for Selecting a Set of Gene Transcripts Discriminating RAS- and PTPN11-Mutated Cells in Acute Lymphoblastic Leukaemia
  19. Nucleophilic Displacements with Pyridine, Quinoline and Acridine Leaving Groups: Rate Variation with Structure of the N-Substituent
  20. Design, synthesis and biological evaluation of trans 2-(thiophen-2-yl)vinyl heteroaromatic iodides
  21. Successful Application of OPLS-DA for the Discrimination of Wild-Type and Mutated Cells in Acute Lymphoblastic Leukemia
  22. N-benzoxazol-2-yl-N′-1-(isoquinolin-3-yl-ethylidene)-hydrazine, a novel compound with antitumor activity, induces radicals and dissipation of mitochondrial membrane potential
  23. Design and synthesis of trans 2-(furan-2-yl)vinyl heteroaromatic iodides with antitumour activity
  24. Identification of genes involved in radiation‐induced G1 arrest
  25. Design, Synthesis, and Biological Evaluation of 4-Alkyliden-beta Lactams:  New Products with Promising Antibiotic Activity Against Resistant Bacteria
  26. Photobehaviour of some 1-heteroaryl-2-(1-methylpyridinium-2-yl)ethene iodides (free and complexed with DNA)
  27. Identification of genes involved in the sensitivity to antitumour drug 17-allylamino,17-demethoxygeldanamycin (17AAG)
  28. Genome-based identification of diagnostic molecular markers for human lung carcinomas by PLS-DA
  29. Design, synthesis and in vitro antitumor activity of new trans 2-[2-(heteroaryl)vinyl]-1,3-dimethylimidazolium iodides
  30. Structure-based rationalization of antitumor drugs mechanism of action by a MIF approach
  31. In vitro antitumor activities of 2,6-di-[2-(Heteroaryl)vinyl]pyridines and pyridiniums
  32. Acid Catalyzed Transesterification as a Route to Poly(3-hydroxybutyrate-co-ε-caprolactone) Copolymers from Their Homopolymers
  33. Studies on the Interactions of the New 2,6-Bis[2-(heteroaryl)vinyl]1-methylpyridinium Cations with the Decamer d(CGTACGTACG)2
  34. Shortcuts in genome-scale cancer pharmacology research from multivariate analysis of the National Cancer Institute gene expression database☆☆Supplementary information is available on Elsevier’s World Wide Web site (http://www.elsevier.nl) or from the c...
  35. A 3D-QSAR Study on the Structural Requirements for Binding to CB1 and CB2 Cannabinoid Receptors
  36. Structural Requirements for Binding to Cannabinoid Receptors
  37. 2,6-Di(heteroarylvinyl)pyridines as new potential �antitumor agents
  38. Chemometrics and cultural heritage
  39. Synthesis and basicity of 2,6-di-[2-(heteroaryl)vinyl]pyridines
  40. Spectroscopic evidence of a free-radical mechanism in the reduction of Schiff bases by formic acid
  41. A New Set of Principal Properties for Heteroaromatics Obtained by GRID
  42. Multiariate characterization, using the SIMCA method, of mortars from two frescoes in Chiaravalle Abbey
  43. Formation of (N-Heteroaryl)heteroarymethanamines from Heteroaromatic Aldehydes and Heteroaromatic Amines
  44. “Classical” and “Magnetic” Aromaticities as new Descriptors for Heteroaromatics in QSAR. Part 3 [1]. Principal Properties for Heteroaromatics
  45. QSAR Study of Heteroaromatic Modifications in the Side Chain of Bradycardic Benzazepinones by Response Surface Modelling [1]
  46. Geographical classification of sicilian olive oils in terms of sterols and fatty acids content
  47. Effects of the Heteroaromatic Moiety on the Antisecretory Activities of Heteroarylmethyl Heteroaryl Sulfides [1]
  48. “Classical” and “Magnetic” Aromaticities as new Descriptors for Heteroaromatics in QSARs. PLS Prediction of Tetrahymena Pyriformis Growth Inhibition by Heteroaromatics
  49. Effects of the heteroaromatic moiety on spectroscopic properties, pKa and reactivity of azoles: A chemometric study
  50. Aromaticity as a Quantitative Concept. 3. Benzo‐fused five‐ and six‐membered heterocycles
  51. Aromaticity as a Quantitative Concept. 2. Sixteen familiar five‐ and six‐membered monocyclic heterocycles
  52. Prediction of gas chromatographic response factors by the PLS method
  53. Aromaticity as a quantitative concept. 1. A statistical demonstration of the orthogonality of classical and magnetic aromaticity in five- and six-membered heterocycles
  54. Carbon‐13 NMR spectra of substituted 2‐thiophenecarboxanilides
  55. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 25. X-Ray structure determinations, crystallographic evidence for steric crowding, and correlation with acceleration of rates
  56. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 22. Reactions with various nucleophiles and a study of the effects of substrate concentration, traces of water, and nature of the gegenion on the rates
  57. Studies of substituent effects by carbon‐13 NMR spectroscopy. VI—Application of multivariate data analysis to 13C NMR chemical shifts of protonated chalcones and thiophene chalcone analogues
  58. Side‐Chain Reactivity of Thiophenes. Thenyl Derivatives
  59. Studies of substituent effects by carbon‐13 NMR spectroscopy.V—Ethyl (E)‐(α‐cyano)cinnamates, (E)‐(α‐cyano)cinnamamides and ethyl (α‐ethoxycarbonyl)cinnamates
  60. Nuclear magnetic resonance studies of (Z)- and (E)-3-amino-3-(p-substituted phenyl)propenenitriles
  61. Qualitative organic analysis
  62. Kinetics and Mechanisms of Nucleophilic Displacements at sp3 Hybridized Carbon Atoms with Heterocyclic Leaving Groups
  63. Use of the Hammett equation in substituted thiophenes
  64. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 19. Chemometric investigation of the simultaneous dependence of S N 2 rates on alkyl group structure and leaving group nucleofugacity
  65. New insights into aliphatic nucleophilic substitution reactions from the use of pyridines as leaving groups
  66. Application of principal components analysis to the evaluation and selection of eluent systems for the thin-layer chromatography of basic and neutral drugs
  67. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 8. Conductimetric and spectrophotometric rate constants for the reactions of pyridinium and related cations with piperidine in chlorobenzene
  68. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 12. Regio- and stereo-chemistry of nucleophilic displacement and solvolysis reactions of N-(α-methylallyl)-and N-(α-phenylethyl)-pyridiniums
  69. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 14. The preparation and reactions of some further α-heteroaryl-pyridinium salts
  70. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 9. N-substituted 2,4,6-triphenylpyridiniums, 5,6-dihydro-2,4-diphenylbenzo[h]quinoliniums, and 5,6,8,9-tetrahydro-7-phenyldibenzo[c,h]acridiniums: kinetic r...
  71. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 4. 2,4,6-Triaryl-N-benzylpyridinium cations: rate variation with electronic effects in the leaving group
  72. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 5. Solvent effects
  73. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. Part 6. Reactions of N-(substituted benzyl)azaheterocyclonium compounds with piperidine
  74. Application of principal component analysis to 13C NMR shifts of chalcones and their thiophene and furan analogues: A useful tool for the shift assignment and for the study of substituent effects
  75. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. 3. N-(substituted benzyl)-2,4,6-triphenylpyridiniums: effects of benzyl substitution on first- and second-order rates
  76. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. 1. 1-Benzyl-2,4,6-triphenylpyridinium
  77. Kinetics and mechanisms of nucleophilic displacements with heterocycles as leaving groups. 2. N-benzylpyridinium cations: rate variation with steric effects in the leaving group
  78. Nucleophilic substitution at sulphonyl sulphur. Part 1. Reactivity of thiophen-2-sulphonyl halides in water and methanol–acetonitrile
  79. The Mass Spectra of Furan Chalcone Analogues
  80. Studies of substituent effects by carbon‐13 NMR spectroscopy. Thiophene and furan chalcone analogues
  81. Unimolecular and bimolecular transfer of N-substituents from pyridinium cations: Evidence for a clear mechanistic changeover
  82. Nucleophilic displacement of N-benzyl groups: effect of pyridinium on rates and mechanism
  83. A C-13 study of the reaction of 2,4,6-triarylpyrylium cations with amines
  84. The protonation of furan- and thiophen-carboxamides
  85. 1,3-Dipolar character of six-membered aromatic rings. Part 45. Photochemically-induced dimerisation of 1-vinyl- and 1-heteroaryl-3-oxidopyridiniums and related compounds
  86. The Reaction of 2,4,6-Triarylpyrylium Cations with Methoxide-Ion
  87. Nucleophilic substitution in the side chain of five-membered heterocycles. 3. Reactions of heterocyclic aldehydes with aniline and with benzoylmethylenetriphenyl phosphorane
  88. Solvent effects in the benzylation of aniline
  89. The acid dissociation of arenesulphonamides: σHetconstants for thia- and oxa-substituents in five-membered S-linked heterocycles and effects of substituents in the N-linked aromatic ring
  90. ChemInform Abstract: CONFORMATION OF 2-THIOPHENESULFONANILIDES FROM DIPOLE MOMENT STUDIES
  91. Conformation of 2-thiophenesulphonanilides from dipole moment studies
  92. Substituent effects in five-membered rings: σHetconstants for thia- and oxa-substituents from the reaction of arenesulphonyl chlorides with aniline
  93. Ultraviolet and infrared absorption spectra of 2-thiophenesulfonamides