All Stories

  1. Structural, morphological, and modeling studies of N-(benzoyloxy)benzamide as a specific inhibitor of Type II inosine monophosphate dehydrogenase
  2. Targeting Viral and Cellular Cysteine Proteases for Treatment of New Variants of SARS-CoV-2
  3. Rutin/Sulfobutylether-β-Cyclodextrin as a Promising Therapeutic Formulation for Ocular Infection
  4. Rutin/Sulfobutylether-β-Cyclodextrin as a Promising Therapeutic Formulation for Ocular Infection
  5. γ‐Cyclodextrins as Supramolecular Reactors for the Three‐component Aza‐Darzens Reaction in Water
  6. Supramolecular biomaterials as drug nanocontainers with iron depletion properties for antimicrobial applications
  7. An Integrated In Silico and In Vitro Approach for the Identification of Natural Products Active against SARS-CoV-2
  8. Discovery of first novel sigma/HDACi dual-ligands with a potent in vitro antiproliferative activity
  9. Antiviral Efficacy of Heparan Sulfate and Enoxaparin Sodium against SARS-CoV-2: An In-Vitro/in-Silico Model
  10. HEMA-based macro and microporous materials for CO2 capture
  11. Insights into the Friedel–Crafts Benzoylation of N-Methylpyrrole inside the Confined Space of the Self-Assembled Resorcinarene Capsule
  12. How can artificial intelligence be utilized for de novo drug design against COVID-19 (SARS-CoV-2)?
  13. Total Bio-Based Material for Drug Delivery and Iron Chelation to Fight Cancer through Antimicrobial Activity
  14. Total Bio-Based Material To Fight Cancer Through Antimicrobial Activity
  15. Progress of the “Molecular Informatics” Section in 2022
  16. Selective noncovalent proteasome inhibiting activity of trifluoromethyl‐containing gem‐quaternary aziridines
  17. Computer-Assisted Design of Peptide-Based Radiotracers
  18. Steered Molecular Dynamics Simulations Study on FABP4 Inhibitors
  19. Design, synthesis, in vitro evaluation, and molecular modeling studies of N‐substituted benzomorphans, analogs of LP2, as novel MOR ligands
  20. Heparan Sulfate and Enoxaparin Interact at the Interface of the Spike Protein of HCoV-229E but Not with HCoV-OC43
  21. Portable Nanocomposite System for Wound Healing in Space
  22. Soluble peptidoglycan fragments produced by Limosilactobacillus fermentum with antiproliferative activity are suitable for potential therapeutic development: A preliminary report
  23. 1,2-Dibenzoylhydrazine as a Multi-Inhibitor Compound: A Morphological and Docking Study
  24. Sponge-like macroporous cyclodextrin-based cryogels for controlled drug delivery
  25. CO2-derived non-isocyanate polyurethanes (NIPUs) and their potential applications
  26. Carbamoyl-Decorated Cyclodextrins for Carbon Dioxide Adsorption
  27. Cyclodextrin-Based Cryogels for Controlled Drug Delivery
  28. Novel Class of Proteasome Inhibitors: In Silico and In Vitro Evaluation of Diverse Chloro(trifluoromethyl)aziridines
  29. Adipocyte fatty acid binding protein 4 (FABP4) inhibitors. An update from 2017 to early 2022
  30. Targeting the SARS-CoV-2 HR1 with Small Molecules as Inhibitors of the Fusion Process
  31. Correction to “Nitric Oxide Photo-Donor Hybrids of Ciprofloxacin and Norfloxacin: A Shift in Activity from Antimicrobial to Anticancer Agents”
  32. Novel Tyrosine Kinase Inhibitors to Target Chronic Myeloid Leukemia
  33. Artificial Intelligence Technologies for COVID-19 De Novo Drug Design
  34. Artificial Intelligence Technologies for COVID-19 De Novo Drug Design
  35. A sustainable porous composite material based on loofah-halloysite for gas adsorption and drug delivery
  36. Carbocation catalysis in confined space: activation of trityl chloride inside the hexameric resorcinarene capsule
  37. Supramolecular catalysis in confined space: making the pyrogallol[4]arene capsule catalytically active in non-competitive solvent
  38. Green Efficient One-Pot Synthesis and Separation of Nitrones in Water Assisted by a Self-Assembled Nanoreactor
  39. Structural and Molecular Insight into Piperazine and Piperidine Derivatives as Histamine H3 and Sigma-1 Receptor Antagonists with Promising Antinociceptive Properties
  40. From Far West to East: Joining the Molecular Architecture of Imidazole-like Ligands in HO-1 Complexes
  41. Natural Substances in the Fight of SARS-CoV-2: A Critical Evaluation Resulting from the Cross-Fertilization of Molecular Modeling Data with the Pharmacological Aspects
  42. Growing the molecular architecture of imidazole-like ligands in HO-1 complexes
  43. Synthesis and in vitro evaluation of chlorogenic acid amides as potential hypoglycemic agents and their synergistic effect with acarbose
  44. Unusual Calixarenes Incorporating Chromene and Benzofuran Moieties Obtained via Propargyl Claisen Rearrangement
  45. Discovery of Novel Acetamide-Based Heme Oxygenase-1 Inhibitors with Potent In Vitro Antiproliferative Activity
  46. Nitric Oxide Photo-Donor Hybrids of Ciprofloxacin and Norfloxacin: A Shift in Activity from Antimicrobial to Anticancer Agents
  47. Shedding Light on the Chemistry and the Properties of Münchnone Functionalized Graphene
  48. Expanding Coefficient: A Parameter To Assess the Stability of Induced-Fit Complexes
  49. Pseudo-Dipeptide Bearing α,α-Difluoromethyl Ketone Moiety as Electrophilic Warhead with Activity against Coronaviruses
  50. Nanosponges based on self-assembled starfish-shaped cucurbit[6]urils functionalized with imidazolium arms
  51. An Integrated Pharmacophore/Docking/3D-QSAR Approach to Screening a Large Library of Products in Search of Future Botulinum Neurotoxin A Inhibitors
  52. Identification of a potent heme oxygenase-2 (HO-2) inhibitor by targeting the secondary hydrophobic pocket of the HO-2 western region
  53. A Rare Natural Benzo[k,l]xanthene as a Turn-Off Fluorescent Sensor for Cu2+ Ion
  54. New Anti SARS-Cov-2 Targets for Quinoline Derivatives Chloroquine and Hydroxychloroquine
  55. Functionalization of Single and Multi-Walled Carbon Nanotubes with Polypropylene Glycol Decorated Pyrrole for the Development of Doxorubicin Nano-Conveyors for Cancer Drug Delivery
  56. Putative Inhibitors of SARS-CoV-2 Main Protease from A Library of Marine Natural Products: A Virtual Screening and Molecular Modeling Study
  57. Sigma Receptor Ligands Carrying a Nitric Oxide Donor Nitrate Moiety: Synthesis, In Silico, and Biological Evaluation
  58. Inhibitors of SARS-CoV-2 Main Protease from a Library of Marine Natural Products: A Virtual Screening and Molecular Modeling Study
  59. New Arylethanolimidazole Derivatives as HO-1 Inhibitors with Cytotoxicity against MCF-7 Breast Cancer Cells
  60. Chromatograpic resolution of phenylethanolic-azole racemic compounds highlighted stereoselective inhibition of heme oxygenase-1 by (R)-enantiomers
  61. Cucurbit[7]uril as a catalytic nanoreactor for one-pot synthesis of isoxazolidines in water
  62. Repurposing of FDA‐Approved Drugs for Treating Iatrogenic Botulism: A Paired 3D‐QSAR/Docking Approach†
  63. Progress in the development of more effective and safer analgesics for pain management
  64. [1]Benzothieno[3,2-d]pyrimidine derivatives as ligands for the serotonergic 5-HT7 receptor
  65. Synergic Interplay Between Halogen Bonding and Hydrogen Bonding in the Activation of a Neutral Substrate in a Nanoconfined Space
  66. Synergic Interplay Between Halogen Bonding and Hydrogen Bonding in the Activation of a Neutral Substrate in a Nanoconfined Space
  67. Supramolecular host-guest interactions of pseudoginsenoside F11 with β- and γ-cyclodextrin: Spectroscopic/spectrometric and computational studies
  68. Computational Tools in the Discovery of FABP4 Ligands: A Statistical and Molecular Modeling Approach
  69. Physicochemical Characterization and Antioxidant Activity Evaluation of Idebenone/Hydroxypropyl-β-Cyclodextrin Inclusion Complex †
  70. Computational Tools in the Discovery of FABP4 Ligands: A Statistical and Molecular Modeling Approach
  71. Metabolic Characterization of Supernatants Produced by Lactobacillus spp. With in vitro Anti-Legionella Activity
  72. Structure-Based Approach for the Prediction of Mu-opioid Binding Affinity of Unclassified Designer Fentanyl-Like Molecules
  73. A molecular hybrid producing simultaneously singlet oxygen and nitric oxide by single photon excitation with green light
  74. Progress in the development of selective heme oxygenase-1 inhibitors and their potential therapeutic application
  75. 3D-QSAR assisted identification of FABP4 inhibitors: An effective scaffold hopping analysis/QSAR evaluation
  76. Hydroxamic Acid-Based Histone Deacetylase (HDAC) Inhibitors Bearing a Pyrazole Scaffold and a Cinnamoyl Linker
  77. Synthesis of Rosmarinic Acid Amides as Antioxidative and Hypoglycemic Agents
  78. Fourfold Filtered Statistical/Computational Approach for the Identification of Imidazole Compounds as HO-1 Inhibitors from Natural Products
  79. FABP4 inhibitors 3D-QSAR model and isosteric replacement of BMS309403 datasets
  80. Gemcitabine anticancer activity enhancement by water soluble celecoxib/sulfobutyl ether-β-cyclodextrin inclusion complex
  81. Morphing of Ibogaine: A Successful Attempt into the Search for Sigma-2 Receptor Ligands
  82. A hexameric resorcinarene capsule as a hydrogen bonding catalyst in the conjugate addition of pyrroles and indoles to nitroalkenes
  83. Metyrapone-β-cyclodextrin supramolecular interactions inferred by complementary spectroscopic/spectrometric and computational studies
  84. A Pseudouridine Isoxazolidinyl Nucleoside Analogue Structural Analysis: A Morphological Approach
  85. Development of new HO-1 inhibitors by a thorough scaffold-hopping analysis
  86. A Structure- and Ligand-Based Virtual Screening of a Database of “Small” Marine Natural Products for the Identification of “Blue” Sigma-2 Receptor Ligands
  87. Targeting heme Oxygenase-1 with hybrid compounds to overcome Imatinib resistance in chronic myeloid leukemia cell lines
  88. Discovery of High-Affinity Cannabinoid Receptors Ligands through a 3D-QSAR Ushered by Scaffold-Hopping Analysis
  89. PEGylate porphyrin-gold nanoparticles conjugates as removable pH-sensor nano-probes for acidic environments
  90. Discovery of benzimidazole-based Leishmania mexicana cysteine protease CPB2.8ΔCTE inhibitors as potential therapeutics for leishmaniasis
  91. Identification of Potentially Potent Heme Oxygenase 1 Inhibitors through 3D‐QSAR Coupled to Scaffold‐Hopping Analysis
  92. Novel Structural Insight into Inhibitors of Heme Oxygenase-1 (HO-1) by New Imidazole-Based Compounds: Biochemical and In Vitro Anticancer Activity Evaluation
  93. Light‐Controlled Simultaneous “On Demand” Release of Cytotoxic Combinations for Bimodal Killing of Cancer Cells
  94. Mild Friedel–Crafts Reactions inside a Hexameric Resorcinarene Capsule: C−Cl Bond Activation through Hydrogen Bonding to Bridging Water Molecules
  95. Mild Friedel–Crafts Reactions inside a Hexameric Resorcinarene Capsule: C−Cl Bond Activation through Hydrogen Bonding to Bridging Water Molecules
  96. Potholing of the hydrophobic heme oxygenase-1 western region for the search of potent and selective imidazole-based inhibitors
  97. Covalently immobilized catalase on functionalized graphene: effect on the activity, immobilization efficiency, and tetramer stability
  98. DNA intercalators based on (1,10-phenanthrolin-2-yl)isoxazolidin-5-yl core with better growth inhibition and selectivity than cisplatin upon head and neck squamous cells carcinoma
  99. Bio-activated intramolecular anti-aza-Michael addition: stereoselective synthesis of hydantoin derivatives
  100. The hexameric resorcinarene capsule as an artificial enzyme: ruling the regio and stereochemistry of a 1,3-dipolar cycloaddition between nitrones and unsaturated aldehydes
  101. (+)-Methyl (1R,2S)-2-{[4-(4-Chlorophenyl)-4-hydroxypiperidin-1-yl]methyl}-1-phenylcyclopropanecarboxylate [(+)-MR200] Derivatives as Potent and Selective Sigma Receptor Ligands: Stereochemistry and Pharmacological Properties
  102. Recent advances in drug discovery of phototherapeutic non-porphyrinic anticancer agents
  103. Comprehensive data on a 2D-QSAR model for Heme Oxygenase isoform 1 inhibitors
  104. Serendipitous discovery of potent human head and neck squamous cell carcinoma anti-cancer molecules: A fortunate failure of a rational molecular design
  105. Ensemble-based ADME-Tox profiling and virtual screening for the discovery of new inhibitors of the Leishmania mexicana cysteine protease CPB2.8ΔCTE
  106. Molecular modeling studies of pseudouridine isoxazolidinyl nucleoside analogues as potential inhibitors of the pseudouridine 5ʹ-monophosphate glycosidase
  107. Hyphenated 3D-QSAR statistical model-scaffold hopping analysis for the identification of potentially potent and selective sigma-2 receptor ligands
  108. Synthesis and evaluation of haloperidol metabolite II prodrugs as anticancer agents
  109. Adipocyte fatty acid binding protein 4 (FABP4) inhibitors. A comprehensive systematic review
  110. Heme Oxygenase Database (HemeOxDB) and QSAR Analysis of Isoform 1 Inhibitors
  111. Development of a Sigma-2 Receptor affinity filter through a Monte Carlo based QSAR analysis
  112. Sigma-2 receptor ligands QSAR model dataset
  113. Repurposing of Human Kinase Inhibitors in Neglected Protozoan Diseases
  114. γ-Cyclodextrin as a Catalyst for the Synthesis of 2-Methyl-3,5-diarylisoxazolidines in Water
  115. The Search for Potent, Small-Molecule HDACIs in Cancer Treatment: A Decade After Vorinostat
  116. S2RSLDB: a comprehensive manually curated, internet-accessible database of the sigma-2 receptor selective ligands
  117. Antiangiogenic Effect of (±)-Haloperidol Metabolite II Valproate Ester [(±)-MRJF22] in Human Microvascular Retinal Endothelial Cells
  118. 5′-Spiro-cyclopropanated lactose derivatives as suitable intermediates for the chain elongation: synthesis of a new 6-deoxy-6-methyl δ-eptulose
  119. Synthesis and characterization of copolycarbonates having azobenzene units in the main chain as an active group for optical logic gate devices
  120. Targeting of the Leishmania mexicana cysteine protease CPB2.8ΔCTE by decorated fused benzo[b]thiophene scaffold
  121. Decorated 6,6′,7,7′-tetrahydro-1H,1′H-2,3′-biindole scaffold as promising candidate for recognition of the CDK2 allosteric site
  122. An α1-adrenergic receptor ligand repurposed as a potent antiproliferative agent for head and neck squamous cell carcinoma
  123. Haloperidol metabolite II prodrug: Asymmetric synthesis and biological evaluation on rat C6 glioma cells
  124. 4-Nitro-2,1,3-benzoxadiazole derivatives as potential fluorescent sigma receptor probes
  125. Repurposing of oxazolone chemistry: gaining access to functionalized graphene nanosheets in a top-down approach from graphite
  126. DNA Recognition with Polycyclic-Aromatic-Hydrocarbon-Presenting Calixarene Conjugates
  127. Production of filmable medium-chain-length polyhydroxyalkanoates produced from glycerol by Pseudomonas mediterranea
  128. Use of Microwave Heating in the Synthesis of Heterocycles from Carbohydrates
  129. Recent advances in small organic molecules as DNA intercalating agents: Synthesis, activity, and modeling
  130. A top–down approach to crystal engineering of a racemic Δ2-isoxazoline
  131. Functional hybrid co-crystals of humic substances: a growth forecast
  132. Prevalence of Oxetanose Forms in the Tautomeric Equilibrium of β-Hydroxy-1,5-dicarbonyl Monosaccharides
  133. Self-Catalyzed Mannich-Type Reaction of Enolizable Cyclic 1,3-Dicarbonyls to Acyclic Nitrones: An Entry to Functionalized β-Enamino Diones
  134. Phosphonated Nucleoside Analogues
  135. Experimental and in silico characterization of a biologically active inosose
  136. Crystal Morphologies and Polymorphs in Tolbutamide Microcrystalline Powder
  137. Histone Methyltransferase Inhibitors: Novel Epigenetic Agents for Cancer Treatment
  138. Histone Methyltransferase Inhibitors: Novel Epigenetic Agents for Cancer Treatment
  139. Synthesis and biological activity of novel bifunctional isoxazolidinyl polycyclic aromatic hydrocarbons
  140. Novel isoxazole polycyclic aromatic hydrocarbons as DNA-intercalating agents
  141. Potassium caffeate/caffeic acid co-crystal: the rat race between the catecholic and carboxylic moieties in an atypical co-crystal
  142. Recent Developments on Rotaxane-Based Shuttles: An Update to 2010
  143. How molecular interactions affect crystal morphology: The case of haloperidol
  144. Design, Synthesis, Molecular Docking and Crystal Structure Prediction of New Azasugar Analogues of α-Glucosidase Inhibitors
  145. From the X-rays to a reliable “low cost” computational structure of caffeic acid: DFT, MP2, HF and integrated molecular dynamics–X-ray diffraction approach to condensed phases
  146. An intriguing U-shaped molecule as possible ionophore for sensor applications: A computational DFT and NMR study
  147. Isoxazolidinyl polycyclic aromatic hydrocarbons as DNA-intercalating antitumor agents
  148. Stereodefined ring contraction-rearrangement of thiocoumarins to new fused benzo[b]thiophene derivatives
  149. β-Cyclodextrin and Caffeine Complexes with Natural Polyphenols from Olive and Olive Oils: NMR, Thermodynamic, and Molecular Modeling Studies
  150. Could N-(diethylcarbamothioyl)benzamide be a good ionophore for sensor membranes?
  151. Structural determinants of resveratrol for cell proliferation inhibition potency: Experimental and docking studies of new analogs
  152. Synthesis of C-4′Truncated Phosphonated Carbocyclic 2′-Oxa-3′-azanucleosides as Antiviral Agents
  153. Biomimetic Synthesis of Natural and “Unnatural” Lignans by Oxidative Coupling of Caffeic Esters
  154. Stereoselective Synthesis and Biological Evaluations of Novel 3′-Deoxy-4′-azaribonucleosides as Inhibitors of Hepatitis C Virus RNA Replication
  155. Structures and properties in different media of N,N-(diethylcarbamothioyl)furan-2-carboxamide: A ionophore for sensor membranes
  156. Recent Developments on Rotaxane-Based Shuttles
  157. 3-Amino-2(5H)furanones as inhibitors of subgenomic hepatitis C virus RNA replication
  158. Cyclopropanation of 5-methylene galactopyranosides by dihalo-, ethoxycarbonyl-, and unsubstituted carbenes
  159. Conversion of Oximes to Carbonyl Compounds by Triscetylpyridinium Tetrakis(oxodiperoxotungsto) Phosphate (PCWP)-mediated Oxidation with Hydrogen Peroxide
  160. Synthesis of Methyleneisoxazolidine Nucleoside Analogues by Microwave-Assisted Nitrone Cycloaddition
  161. Phosphonated Carbocyclic 2‘-Oxa-3‘-azanucleosides as New Antiretroviral Agents
  162. A Novel Class of Modified Nucleosides: Synthesis of Alkylidene Isoxazolidinyl Nucleosides Containing Thymine
  163. A DFT study on the 1,3-dipolar cycloaddition reactions of C-(hetaryl) nitrones with methyl acrylate and vinyl acetate
  164. Synthesis and biological evaluation of phosphonated carbocyclic 2′-oxa-3′-aza-nucleosides
  165. Binding of a non-ionic pyrenylisoxazolidine derivative to double-stranded polynucleotides: spectroscopic and molecular modelling studies
  166. Synthesis and Biological Activity of Isoxazolidinyl Polycyclic Aromatic Hydrocarbons:  Potential DNA Intercalators
  167. Corrigendum to “Enantioselective synthesis of N,O-psiconucleosides”
  168. Zinc(II) Triflate-Controlled 1,3-Dipolar Cycloadditions of C -(2-Thiazolyl)nitrones:  Application to the Synthesis of a Novel Isoxazolidinyl Analogue of Tiazofurin
  169. Synthesis of functionalized polyhedral oligomeric silsesquioxane (POSS) macromers by microwave assisted 1,3-dipolar cycloaddition
  170. From Amino Acids to Enantiopure Bicyclic Isoxazolidinylpyridin-4(1H)-ones through Intramolecular Nitrone Cycloadditions
  171. Synthesis of Phosphonated Carbocyclic 2‘-Oxa-3‘-aza-nucleosides:  Novel Inhibitors of Reverse Transcriptase
  172. Reactions of Benzonitrile Oxide with Methoxypyrimidines and Pyrimidones
  173. C-Alkoxycarbonyl Nitrones: Building Blocks for the Synthesis of Butenolides, Lactams and Modified Nucleosides
  174. Synthesis of pyrimidine-containing 3-aminobutenolides
  175. A DFT rationalization for the observed regiochemistry in the nitrile oxide cycloaddition with anthracene and acridine
  176. From cyclopentadiene to isoxazoline–carbocyclic nucleosides: a rapid access to biological molecules through nitrosocarbonyl chemistry
  177. Steric course of some cyclopropanation reactions of L-threo-hex-4-enopyranosides
  178. Diastereoselective synthesis of homo-N,O-nucleosides
  179. Diastereo- and Enantioselective Synthesis of 1′-C-BranchedN,O-Nucleosides
  180. Diastereo- and enantioselective synthesis of N,O-nucleosides
  181. Enantioselective synthesis of N,O-psiconucleosides
  182. Enantioselective Syntheses and Cytotoxicity ofN,O-Nucleosides
  183. Isoxazolidine analogues of pseudouridine: a new class of modified nucleosides
  184. A DFT study on the 1,3-dipolar cycloaddition reactions of C-(methoxycarbonyl)-N-methyl nitrone with methyl acrylate and vinyl acetate
  185. New Rearrangement of 4-Isoxazoline System:  Conversion of Ketones into α,β-Unsaturated Amides
  186. Enantioselective synthesis of isoxazolidinyl nucleosides containing uracil, 5-fluorouracil, thymine and cytosine as new potential anti-HIV drugs
  187. Syntheses of new chiral bicyclic sultams and their use as auxiliaries in asymmetric conjugate addition of Grignard reagents
  188. Intramolecular Cycloadditions of α-Allyloxycarbonylnitrones:  Stereoselective Synthesis of 3-Amino-2(5H)furanones
  189. Diastereoselective Synthesis ofN,O-Psiconucleosides, a New Class of Modified Nucleosides
  190. Enantioselective synthesis of 4-hydroxy-d-pyroglutamic acid derivatives by an asymmetric 1,3-dipolar cycloaddition
  191. Modified nucleosides. A general and diastereoselective approach to N,O-psiconucleosides
  192. A Stereoselective Approach to Isoxazolidinyl Nucleosides
  193. Stereoselective synthesis of homochiral annulated sultams via intramolecular cycloaddition reactions
  194. Diastereoselective synthesis of N,O-psiconucleosides via 1,3-dipolar cycloadditions
  195. Diastereoselective and enantioselective synthesis of 4′-aza analogues of 2′,3′-dideoxynucleosides
  196. Cycloadditions of mesitonitrile oxide with amino- and nitrostilbenes†
  197. An Unusual Route for the Regioselective Acylation of Polycyclic Aromatic Hydrocarbons: Nitrile Oxide Addition Followed by Isoxazoline Degradation
  198. Homochiral α-d- and β-d-Isoxazolidinylthymidines via 1,3-Dipolar Cycloaddition†
  199. Stereoselective Synthesis of Enantiomerically Pure Isoxa-zolidine-fused d-Lactams
  200. Stereoselective Synthesis of 2‘-Amino-2‘,3‘-dideoxynucleosides by Nitrone 1,3-Dipolar Cycloaddition:  A New Efficient Entry Toward d4T and Its 2-Methyl Analogue †
  201. Cycloaddition of nitrile oxides to aza-analogues of phenanthrene
  202. A general synthetic approach to 5-alkyl-2(5H)furanonesvia 1,3-dipolar cycloaddition
  203. THE REACTION OF UNSATURATED CARBONYL COMPOUNDS WITH "ACTIVATED" SULFUR PART 3.1 REACTION COURSE
  204. The Reaction of Unsaturated Carbonyl Compounds with “Activated” Sulfur. Part 3.1Reaction Course
  205. The Reaction of Unsaturated Carbonyl Compounds with "Activated" Sulfur (II). Formation of Cyclic Disulfide and Polysulfides
  206. Cycloadditions of Mesitonitrile Oxide with Hydroxy- and Methoxy-substituted Stilbenes. A Directing Hydrogen Bonding Model
  207. Biomimetic Supramolecular Biophenol−Carbohydrate and Biophenol−Protein Models by NMR Experiments
  208. Stereoselective synthesis of isoxazole and pyrazole annulated sultams via intramolecular 1,3-dipolar cycloaddition reactions
  209. Intramolecular nitrone cycloaddition: Stereoselective synthesis of piperidine systems
  210. Intramolecular nitrile oxide cycloaddition (INOC) of substituted amido-oximes
  211. An asymmetric approach to pyrrolidinone and pyrrolizidinone systems by intramolecular oxime-olefin cycloaddition
  212. Modified dideoxynucleosides: Synthesis of 2′-N-alkyl-3′-hydroxyalkyl-1′,2′-isoxazolidinyl thymidine and 5-fluorouridine derivatives
  213. Synthesis of 1-alkyl-3-dialkylaminoalkylamine[1]benzo-thieno[2,3-b]pyrazin-2(1H))-ones and their ability to antagonize KCl-induced contractions
  214. Ring opening of the isoxazolidine system: A new synthesis of 3-amino-2(5H)furanones
  215. α-Amino acids as chiral educts for stereoselective syntheses of pyrrolidine and pyrrolizidine systems
  216. Ring-opening of isoxazolidine nucleus: Competitive formation of α,β-enones and tetrahydro-1,3-oxazines
  217. Stereoselective synthesis of fused γ-lactams by intramolecular nitrone cycloaddition
  218. Stereoselective control in 1,3-dipolar cycloaddition of nitrones to substituted styrenes
  219. The Reaction of Unsaturated Carbonyl Compounds with "Activated" Sulfur
  220. Functionalized g-Lactones via Intramolecular Nitrile Oxide Cycloaddition
  221. A New Synthesis of Streptomyces Lactones by 1,3-Dipolar Cycloaddition
  222. Ring-Opening of 4-Isoxazolines: Competitive Formation of Enamino Derivatives and a,b-Enones
  223. Formation of Isoxazolines and Isoxazoles Via Dipolar Cycloaddition by Catalytic Oxidation of Aldoximes with Hydrogen Peroxide and W(Vi) Peroxo Complexes
  224. Novel approach to the ring-opening of 4-isoxazolines: One-pot synthesis of α,β-enones
  225. One-flask transformation of secondary amines to nitrones by oxidation with hydrogen peroxide mediated by triscetylpyridinium tetrakis oxodiperoxotungsto-phosphate (PCWP). Some mechanistic considerations
  226. Rearrangement of o-alkynyl substituted α-diazoacetophenones. Conversion to β-naphthols via arylketene intermediates