All Stories

  1. Mechanochemical Reductive Amination of Aldehydes and Ketones: Solid-State Synthesis of the Antiparkinsonian Drugs Rasagiline and Safinamide
  2. 2-Styrylquinolines with Push-Pull Architectures as Sensors for β-Amyloid Aggregation with Theranostic Properties
  3. Regioselective N-2 Alkylation of Tetrazoles with Phenacyl Halides under Mechanochemical Conditions and Its Application to a Solid-State Synthesis of the Antiepileptic Drug Cenobamate
  4. Network-Based Drug Optimization toward the Treatment of Parkinson’s Disease: NRF2, MAO-B, Oxidative Stress, and Chronic Neuroinflammation
  5. Twenty-first century antiepileptic drugs. An overview of their targets and synthetic approaches
  6. Dual Antitubercular and Antileishmanial Profiles of Quinoxaline Di-N-Oxides Containing an Amino Acidic Side Chain
  7. Fluorimetric Detection of Insulin Misfolding by Probes Derived from Functionalized Fluorene Frameworks
  8. Structure-Antitumor Activity Relationships of Aza- and Diaza-Anthracene-2,9,10-Triones and Their Partially Saturated Derivatives
  9. Cyclodextrin Inclusion Complexes for Improved Drug Bioavailability and Activity: Synthetic and Analytical Aspects
  10. Rapid Assembly of Functionalized 2H-Chromenes and 1,2-Dihydroquinolines via Microwave-Assisted Secondary Amine-Catalyzed Cascade Annulation of 2-O/N-Propargylarylaldehydes with 2,6-Dialkylphenols
  11. Quinones as Neuroprotective Agents
  12. m-Terphenylamines, Acting as Selective COX-1 Inhibitors, Block Microglia Inflammatory Response and Exert Neuroprotective Activity
  13. Small-molecule theranostics in Alzheimer's disease
  14. A New Method for the Introduction of an Acylsulfonamide Moiety Applied to a 3-Substituted Functionalized Indole Framework ­Related to the Welwitindolinone Alkaloids
  15. 2-(3-Bromophenyl)imidazo[2,1-b]oxazole
  16. Anticancer drugs acting on signaling pathways, part 1: Tyrosine kinase inhibitors
  17. Anticancer drugs acting on signaling pathways, part 2: Inhibitors of serine-threonine kinases and miscellaneous signaling pathways
  18. Anticancer drugs targeting tubulin and microtubules
  19. Anticancer drugs that interact with the DNA minor groove
  20. Anticancer drugs that modulate hormone action
  21. Anticancer strategies involving radical species
  22. Antimetabolites
  23. Cancer chemoprevention
  24. Cancer immunotherapy
  25. DNA alkylating agents
  26. DNA intercalation and topoisomerase inhibition
  27. Drug targeting in anticancer chemotherapy
  28. Drugs that modulate resistance to antitumor agents
  29. Epigenetic therapy of cancer
  30. General aspects of cancer therapy
  31. Miscellaneous small- molecule and biological approaches to targeted cancer therapy
  32. Protein degradation-based cancer therapy
  33. Small Molecules as Toll-like Receptor 4 Modulators Drug and In-House Computational Repurposing
  34. An Efficient Synthesis of a Highly Functionalized Dihydrobenzo­thiophene Derivative: A Ring-Contracted Analogue of the Anti-inflammatory Drug Propoxicam
  35. Fluorescence Sensors Based on Hydroxycarbazole for the Determination of Neurodegeneration-Related Halide Anions
  36. Approaches to the Potential Therapy of COVID-19: A General Overview from the Medicinal Chemistry Perspective
  37. Enantioselective Synthesis and Pharmacological Evaluation of Aza-CGP37157–Lipoic Acid Hybrids for the Treatment of Alzheimer’s Disease
  38. Enantioselective catalytic Povarov reactions
  39. Curcumin-Piperlongumine Hybrids with a Multitarget Profile Elicit Neuroprotection in In Vitro Models of Oxidative Stress and Hyperphosphorylation
  40. Enhanced Stability and Bioactivity of Natural Anticancer Topoisomerase I Inhibitors through Cyclodextrin Complexation
  41. Mechanochemical Synthesis of Primary Amides
  42. Neuroprotective Action of Multitarget 7-Aminophenanthridin-6(5H)-one Derivatives against Metal-Induced Cell Death and Oxidative Stress in SN56 Cells
  43. Bisavenathramide Analogues as Nrf2 Inductors and Neuroprotectors in In Vitro Models of Oxidative Stress and Hyperphosphorylation
  44. (2S*,4S*)-4-[(E)-(2,2-Dimethylhydrazono)methyl]-6-methoxy-4-methyl-2-[(E)-styryl]-1,2,3,4-tetrahydroquinoline
  45. (E)-3-((2-Fluorophenyl)(hydroxy)methylene)imidazo[1,2-a]pyridin-2(3H)-one
  46. Mechanochemical Aza-Vinylogous Povarov Reactions for the Synthesis of Highly Functionalized 1,2,3,4-Tetrahydroquinolines and 1,2,3,4-Tetrahydro-1,5-Naphthyridines
  47. Sustainable Access to Acridin-9-(10H)ones with an Embedded m-Terphenyl Moiety Based on a Three-Component Reaction
  48. Synthesis of 1,4-Diazepanes and Benzo[b][1,4]diazepines by a Domino Process Involving the In Situ Generation of an Aza-Nazarov Reagent
  49. Antioxidant, Anti-inflammatory and Neuroprotective Profiles of Novel 1,4-Dihydropyridine Derivatives for the Treatment of Alzheimer’s Disease
  50. Antioxidants as Molecular Probes: Structurally Novel Dihydro-m-Terphenyls as Turn-On Fluorescence Chemodosimeters for Biologically Relevant Oxidants
  51. NRF2 Regulation Processes as a Source of Potential Drug Targets against Neurodegenerative Diseases
  52. D-Ring-Modified Analogues of Luotonin A with Reduced Planarity: Design, Synthesis, and Evaluation of Their Topoisomerase Inhibition-Associated Cytotoxicity
  53. Front Cover: Rearrangement Reactions in Aza-Vinylogous Povarov Products: Metal-Free Synthesis of C3 -Functionalized Quinolines and Studies on their Synthetic Application (Eur. J. Org. Chem. 38/2019)
  54. Proline and its Derivatives as Organocatalysts for Multi‐ Component Reactions in Aqueous Media: Synergic Pathways to the Green Synthesis of Heterocycles
  55. Rearrangement Reactions in Aza-Vinylogous Povarov Products: Metal-Free Synthesis of C3 -Functionalized Quinolines and Studies on their Synthetic Application
  56. Design and synthesis of A- and D ring-modified analogues of luotonin A with reduced planarity
  57. Spirooxindole-pyrrolidine heterocyclic hybrids promotes apoptosis through activation of caspase-3
  58. Structure-activity relationships and mechanistic studies of novel mitochondria-targeted, leishmanicidal derivatives of the 4-aminostyrylquinoline scaffold
  59. Progress in the Chemistry of Tetrahydroquinolines
  60. Diversity‐Oriented Synthesis of Complex Pyrrole‐Based Architectures from Very Simple Starting Materials
  61. Multicomponent domino protocol for the stereoselective synthesis of novel pyrrolo[3,2-c]quinolinone hybrid heterocycles
  62. Heterogeneous Amberlyst-15-catalyzed synthesis of complex hybrid heterocycles containing [1,6]-naphthyridine under metal-free green conditions
  63. Oxidant-free, three-component synthesis of 7-amino-6H-benzo[c]chromen-6-ones under green conditions
  64. The Hantzsch Pyrrole Synthesis: Non-conventional Variations and Applications of a Neglected Classical Reaction
  65. Three-Component Synthesis of a Library of m-Terphenyl Derivatives with Embedded β-Aminoester Moieties
  66. Multicomponent Domino Synthesis, Anticancer Activity and Molecular Modeling Simulation of Complex Dispirooxindolopyrrolidines
  67. Highly functionalized pyrrolidine analogues: stereoselective synthesis and caspase-dependent apoptotic activity
  68. Multicomponent mechanochemical synthesis
  69. A systematic 1 H- and 13 C-NMR spectral analysis of bicyclo[n.3.1]alkanone systems: Determination of the relative configuration of the stereogenic centres and conformation of the six-membered ring
  70. One-Pot Synthesis of Functionalized Carbazoles via a CAN-Catalyzed Multicomponent Process Comprising a C–H Activation Step
  71. Mild and General Synthesis of Pyrrolo[2,1-a]isoquinolines and Related Polyheterocyclic Frameworks from Pyrrole Precursors Derived from a Mechanochemical Multicomponent Reaction
  72. Synthesis of 6,12-Epiminodibenzo[b,f][1,5]diazocines via an Ytterbium Triflate-Catalyzed, AB2 Three-Component Reaction
  73. Three-component synthesis of highly functionalized aziridines containing a peptide side chain and their one-step transformation into β-functionalized α-ketoamides
  74. From Simple Cyclic 1,3-Ketoamides to Complex Spirolactams by Supported Heterogeneous Organocatalysis with PS-BEMP
  75. Tetrahydroisoquinoline-Derived Urea and 2,5-Diketopiperazine Derivatives as Selective Antagonists of the Transient Receptor Potential Melastatin 8 (TRPM8) Channel Receptor and Antiprostate Cancer Agents
  76. One-Pot Access to a Library of Dispiro Oxindole-pyrrolidine/pyrrolothiazole-thiochromane Hybrids via Three-Component 1,3-Dipolar Cycloaddition Reactions
  77. Three-Component Synthesis of Pyrrole-Related Nitrogen Heterocycles by a Hantzsch-Type Process: Comparison between Conventional and High-Speed Vibration Milling Conditions
  78. A Sustainable Approach to the Stereoselective Synthesis of Diazaheptacyclic Cage Systems Based on a Multicomponent Strategy in an Ionic Liquid
  79. ChemInform Abstract: Dipolar Cycloaddition-Based Multicomponent Reactions in Ionic Liquids: A Green, Fully Stereoselective Synthesis of Novel Polycyclic Cage Systems with the Generation of Two New Azaheterocyclic Rings.
  80. ChemInform Abstract: Expedient, Catalyst-Free, Three-Component Synthesis of Fused Tetrahydropyridines in Water.
  81. Efficient synthesis of 2-acylquinolines based on an aza-vinylogous Povarov reaction
  82. Three-component access to 2-pyrrolin-5-ones and their use in target-oriented and diversity-oriented synthesis
  83. Synthesis of 5,6-Dihydrodibenzo[b,h][1,6]naphthyridines via Copper Bromide Catalyzed Intramolecular [4 + 2] Hetero-Diels–Alder Reactions
  84. Straightforward synthesis of pyrrolo[3,4-b]quinolines through intramolecular Povarov reactions
  85. ChemInform Abstract: An Efficient Synthesis of N-Substituted 3-Nitrothiophen-2-amines.
  86. ChemInform Abstract: Highly Efficient Regioselective Synthesis of Pyrroles via a Tandem Enamine Formation-Michael Addition-Cyclization Sequence under Catalyst- and Solvent-Free Conditions.
  87. An efficient synthesis of N-substituted 3-nitrothiophen-2-amines
  88. An Expedient Regio- and Diastereoselective Synthesis of Hybrid Frameworks with Embedded Spiro[9,10]dihydroanthracene [9,3′]-pyrrolidine and Spiro[oxindole-3,2′-pyrrolidine] Motifs via an Ionic Liquid-Mediated Multicomponent Reaction
  89. ChemInform Abstract: Palladium(II)-Catalyzed Intramolecular Carboxypalladation-Olefin Insertion Cascade: Direct Access to Indeno[1,2-b]furan-2-ones.
  90. Dipolar Cycloaddition-Based Multicomponent Reactions in Ionic Liquids: A Green, Fully Stereoselective Synthesis of Novel Polycyclic Cage Systems with the Generation of Two New Azaheterocyclic Rings
  91. ChemInform Abstract: Lewis Acid-Catalyzed Generation of C-C and C-N Bonds on π-Deficient Heterocyclic Substrates.
  92. Six-Membered Heterocycles
  93. ChemInform Abstract: One-Pot α-Amidosulfone-Mediated Variation of the Pictet-Spengler Tetrahydroisoquinoline Synthesis, Suitable for Amide-Type Substrates.
  94. ChemInform Abstract: A Heavy Metal- and Oxidant-Free, One-Pot Synthesis of Pyridines and Fused Pyridines Based on a Lewis Acid-Catalyzed Multicomponent Reaction.
  95. Imaging of β-amyloid plaques by near infrared fluorescent tracers: a new frontier for chemical neuroscience
  96. Palladium(ii)-catalyzed intramolecular carboxypalladation–olefin insertion cascade: direct access to indeno[1,2-b]furan-2-ones
  97. Highly efficient regioselective synthesis of pyrroles via a tandem enamine formation–Michael addition–cyclization sequence under catalyst- and solvent-free conditions
  98. Cancer Chemoprevention
  99. Preface
  100. DNA Alkylating Agents
  101. Biological Therapy of Cancer
  102. Anticancer Drugs Targeting Tubulin and Microtubules
  103. Drug Targeting in Anticancer Chemotherapy
  104. Anticancer Drugs Acting via Radical Species
  105. Anticancer Drugs That Modulate Hormone Action
  106. Epigenetic Therapy of Cancer
  107. General Aspects of Cancer Chemotherapy
  108. Drugs That Modulate Resistance to Antitumor Agents
  109. Antimetabolites That Interfere with Nucleic Acid Biosynthesis
  110. Other Nonbiological Approaches to Targeted Cancer Chemotherapy
  111. Anticancer Drugs That Interact with the DNA Minor Groove
  112. Other Anticancer Drugs Targeting DNA and DNA-Associated Enzymes
  113. Drugs That Inhibit Signaling Pathways for Tumor Cell Growth and Proliferation
  114. ChemInform Abstract: Fully Diastereoselective Synthesis of Polysubstituted, Functionalized Piperidines and Decahydroquinolines Based on Multicomponent Reactions Catalyzed by Cerium(IV) Ammonium Nitrate.
  115. Expedient, catalyst-free, three-component synthesis of fused tetrahydropyridines in water
  116. Lewis Acid-Catalyzed Generation of CC and CN Bonds on π-Deficient Heterocyclic Substrates
  117. Axial Chirality of 4-Arylpyrazolo[3,4-b]pyridines. Conformational Analysis and Absolute Configuration
  118. ChemInform Abstract: Recent Advances in the Synthesis of Pyrroles by Multicomponent Reactions
  119. One-Pot α-Amidosulfone-Mediated Variation of the Pictet-Spengler Tetrahydroisoquinoline Synthesis, Suitable for Amide-Type Substrates
  120. Fully Diastereoselective Synthesis of Polysubstituted, Functionalized Piperidines and Decahydroquinolines Based on Multicomponent Reactions Catalyzed by Cerium(IV) Ammonium Nitrate
  121. Montmorillonite Clay-Promoted, Solvent-Free Cross-Aldol Condensations under Focused Microwave Irradiation
  122. B-Ring-Aryl Substituted Luotonin A Analogues with a New Binding Mode to the Topoisomerase 1-DNA Complex Show Enhanced Cytotoxic Activity
  123. New 5-Unsubstituted Dihydropyridines with Improved CaV1.3 Selectivity as Potential Neuroprotective Agents against Ischemic Injury
  124. A catalyst-free multicomponent domino sequence for the diastereoselective synthesis of (E)-3-[2-arylcarbonyl-3-(arylamino)allyl]chromen-4-ones
  125. ChemInform Abstract: A β-Enaminone-Initiated Multicomponent Domino Reaction for the Synthesis of Indoloquinolizines and Benzoquinolizines from Acyclic Precursors.
  126. Concise synthesis of atorvastatin lactone under high-speed vibration milling conditions
  127. Recent advances in the synthesis of pyrroles by multicomponent reactions
  128. A heavy metal- and oxidant-free, one-pot synthesis of pyridines and fused pyridines based on a Lewis acid-catalyzed multicomponent reaction
  129. Synthesis of Heterocycles Through Multicomponent Reactions in Water
  130. ChemInform Abstract: A New CAN-Catalyzed Domino Process Related to the Nenitzescu Reaction: Very Concise Access to Fused ortho-Indolequinones from Simple Precursors.
  131. Modulation of Prion by Small Molecules: From Monovalent to Bivalent and Multivalent Ligands
  132. ChemInform Abstract: Chemodivergent, Multicomponent Domino Reactions in Aqueous Media: L-Proline-Catalyzed Assembly of Densely Functionalized 4H-Pyrano[2,3-c]pyrazoles and Bispyrazolyl Propanoates from Simple, Acyclic Starting Materials.
  133. ChemInform Abstract: Michael Additions in Aqueous Media: “On-Water” and “In-Water” Processes from α-Nitro Ketones and Their Anions.
  134. A β-Enaminone-Initiated Multicomponent Domino Reaction for the Synthesis of Indoloquinolizines and Benzoquinolizines from Acyclic Precursors
  135. A new CAN-catalyzed domino process related to the Nenitzescu reaction: very concise access to fused ortho-indolequinones from simple precursors
  136. Editorial (Hot Topic: Multibond Forming Reactions: A New Frontier in the Synthesis of Heterocycles)
  137. L-Proline Catalysed Domino Reactions for the Synthesis of Heterocycles
  138. ChemInform Abstract: Diastereoselective, Multicomponent Access to trans-2-Aryl-4-arylamino-1,2,3,4-tetrahydroquinolines via an AA′BC Sequential Four-Component Reaction and Their Application to 2-Arylquinoline Synthesis.
  139. ChemInform Abstract: Microwave-Assisted, Sequential Four-Component Synthesis of Polysubstituted 5,6-Dihydroquinazolinones (IV) from Acyclic Precursors and a Mild, Halogenation-Initiated Method for Their Aromatization [→(V)] under Focused Microwave Irradia
  140. ChemInform Abstract: Three-Component Access to Pyrroles Promoted by the CAN-Silver Nitrate System under High-Speed Vibration Milling Conditions: A Generalization of the Hantzsch Pyrrole Synthesis.
  141. Synthesis of a D Ring-Functionalized Derivative of the Epiwelwistatin Tetracyclic Core
  142. Michael Additions in Aqueous Media: “On-Water” and “In-Water” Processes from α-Nitro Ketones and Their Anions
  143. ChemInform Abstract: Privileged Scaffolds in Synthesis: 2,5-Piperazinediones as Templates for the Preparation of Structurally Diverse Heterocycles
  144. A Fluorescent Styrylquinoline with Combined Therapeutic and Diagnostic Activities against Alzheimer’s and Prion Diseases
  145. Three-component access to pyrroles promoted by the CAN–silver nitrate system under high-speed vibration milling conditions: a generalization of the Hantzsch pyrrole synthesis
  146. Identification of 4,6-diaryl-1,4-dihydropyridines as a new class of neuroprotective agents
  147. Diastereoselective, multicomponent access to trans-2-aryl-4-arylamino-1,2,3,4-tetrahydroquinolines via an AA′BC sequential four-component reaction and their application to 2-arylquinoline synthesis
  148. Chemodivergent, multicomponent domino reactions in aqueous media: l-proline-catalyzed assembly of densely functionalized 4H-pyrano[2,3-c]pyrazoles and bispyrazolyl propanoates from simple, acyclic starting materials
  149. Microwave-assisted, sequential four-component synthesis of polysubstituted 5,6-dihydroquinazolinones from acyclic precursors and a mild, halogenation-initiated method for their aromatization under focused microwave irradiation
  150. Solvent- and chromatography-free amination of π-deficient nitrogen heterocycles under microwave irradiation. A fast, efficient and green route to 9-aminoacridines, 4-aminoquinolines and 4-aminoquinazolines and its application to the synthesis of the dr...
  151. ChemInform Abstract: Facile Ionic Liquid-Mediated, Three-Component Sequential Reactions for the Green, Regio- and Diastereoselective Synthesis of Furocoumarins.
  152. One-Pot Access to a Library of Structurally Diverse Nicotinamide Derivatives via a Three-Component Formal Aza [3 + 3] Cycloaddition
  153. Fluorescence properties of the anti-tumour alkaloid luotonin A and new synthetic analogues: pH modulation as an approach to their fluorimetric quantitation in biological samples
  154. ChemInform Abstract: Aryl Grignard Reagents in Chemodivergent N- and C-Arylations: Concise Access to Two Families of Tetracyclic Fused Carbazoles from 6-Nitroquinolines.
  155. ChemInform Abstract: Domino Reactions in Water: Diastereoselective Synthesis of Densely Functionalized Indolyldihydrofuran Derivatives.
  156. Facile ionic liquid-mediated, three-component sequential reactions for the green, regio- and diastereoselective synthesis of furocoumarins
  157. ChemInform Abstract: Synthesis of Polysubstituted, Functionalized Quinolines Through a Metal-Free Domino Process Involving a C4-C3Functional Group Rearrangement.
  158. Synthesis of Polysubstituted, Functionalized Quinolines through a Metal-Free Domino Process Involving a C 4 –C 3 Functional Group Rearrangement
  159. Aryl Grignard Reagents in Chemodivergent N- and C-Arylations: Concise Access to Two Families of Tetracyclic Fused Carbazoles from 6-Nitroquinolines
  160. ChemInform Abstract: L-Proline-Catalyzed Sequential Four-Component “On Water” Protocol for the Synthesis of Structurally Complex Heterocyclic ortho-Quinones.
  161. New Types of Reactivity of α,β‐Unsaturated N , N ‐Dimethylhydrazones: Chemodivergent Diastereoselective Synthesis of Functionalized Tetrahydroquinolines and Hexahydropyrrolo[3,2‐ b ...
  162. ChemInform Abstract: A General Protocol for the Solvent- and Catalyst-Free Synthesis of 2-Styrylquinolines under Focused Microwave Irradiation.
  163. ChemInform Abstract: Brief, Efficient and Highly Diastereoselective Synthesis of (.+-.)-Pumiliotoxin C Based on the Generation of an Octahydroquinoline Precursor via a Four-Component Reaction.
  164. ChemInform Abstract: L-Proline-Catalyzed Three-Component Domino Reactions for the Diastereoselective Synthesis of 5,6-Disubstituted 3-Thiomorpholinones.
  165. Privileged scaffolds in synthesis: 2,5-piperazinediones as templates for the preparation of structurally diverse heterocycles
  166. A one-pot sequence for the efficient synthesis of highly functionalized macrocarbocycles or bridged 2,8-dioxabicyclo[3.2.1]octanes from 1-nitrobicyclic compounds
  167. Domino reactions in water: diastereoselective synthesis of densely functionalized indolyldihydrofuran derivatives
  168. A systematic study of two complementary protocols allowing the general, mild and efficient deprotection of N-pivaloylindoles
  169. ChemInform Abstract: Advances in the Chemistry of Tetrahydroquinolines
  170. ChemInform Abstract: A Facile, Three-Component Domino Protocol for the Microwave-Assisted Synthesis of Functionalized Naphtho[2,3-b]furan-4,9-diones in Water.
  171. Advances in the Chemistry of Tetrahydroquinolines
  172. ChemInform Abstract: Domino Reactions for the Synthesis of Bridged Bicyclic Frameworks: Fast Access to Bicyclo[n.3.1]alkanes
  173. A General Protocol for the Solvent- and Catalyst-Free Synthesis of 2-Styrylquinolines under Focused Microwave Irradiation
  174. l-Proline-catalysed three-component domino reactions for the diastereoselective synthesis of 5,6-disubstituted 3-thiomorpholinones
  175. Two chemodivergent anionic domino processes from cyclic α-nitroketones and aromatic aldehydes
  176. ChemInform Abstract: A Facile Three-Component [3 + 2]-Cycloaddition/Annulation Domino Protocol for the Regio- and Diastereoselective Synthesis of Novel Penta- and Hexacyclic Cage Systems, Involving the Generation of Two Heterocyclic Rings and Five Contigu
  177. ChemInform Abstract: Synthesis of Benzo- and Naphtho-Fused Bicyclo[n.3.1]alkane Frameworks with a Bridgehead Nitrogen Function by Palladium-Catalyzed Intramolecular α′-Arylation of α-Nitroketones.
  178. Antimycobacterial activity of novel 1,2,4-oxadiazole-pyranopyridine/chromene hybrids generated by chemoselective 1,3-dipolar cycloadditions of nitrile oxides
  179. ChemInform Abstract: A Three-Component Domino Protocol for the Facile Synthesis of Highly Functionalized Tetrahydroisoquinolines by Creation of Their Benzene Ring.
  180. New four-component reactions in water: a convergent approach to the metal-free synthesis of spiro[indoline/acenaphthylene-3,4′-pyrazolo[3,4-b]pyridine derivatives
  181. A facile three-component [3+2]-cycloaddition/annulation domino protocol for the regio- and diastereoselective synthesis of novel penta- and hexacyclic cage systems, involving the generation of two heterocyclic rings and five contiguous stereocenters
  182. A General, Diastereoselective Synthesis of Highly Functionalized Bicyclo[n.3.1]alkane Systems Based on an Anionic Domino Reaction of α-Nitrocycloalkanones
  183. ChemInform Abstract: CAN-Promoted, Diastereoselective Synthesis of Fused 2,3-Dihydrofurans and Their Transformation into Tetrahydroindoles.
  184. A three-component domino protocol for the facile synthesis of highly functionalized tetrahydroisoquinolines by creation of their benzene ring
  185. ChemInform Abstract: Multicomponent Reactions for the Synthesis of Pyrroles
  186. ChemInform Abstract: Three-Component, Diastereoselective Synthesis of Highly Functionalized Indan Derivatives Based on an Anionic Domino Sequence from α-Nitroketones.
  187. Brief, efficient and highly diastereoselective synthesis of (±)-pumiliotoxin C based on the generation of an octahydroquinoline precursor via a four-component reaction
  188. Domino reactions for the synthesis of bridged bicyclic frameworks: fast access to bicyclo[n.3.1]alkanes
  189. Antimycobacterial activity of spirooxindolo-pyrrolidine, pyrrolizine and pyrrolothiazole hybrids obtained by a three-component regio- and stereoselective 1,3-dipolar cycloaddition
  190. 1,3-Dipolar cycloadditions from tricyclic hemiaminals. Synthesis of the quinocarcin core through catalyst-free generation of azomethine ylides
  191. Synthesis of benzo- and naphtho-fused bicyclo[n.3.1]alkane frameworks with a bridgehead nitrogen function by palladium-catalyzed intramolecular α′-arylation of α-nitroketones
  192. Eco-friendly liquid chromatographic separations based on the use of cyclodextrins as mobile phase additives
  193. l-Proline-catalysed sequential four-component “on water” protocol for the synthesis of structurally complex heterocyclic ortho-quinones
  194. A facile, three-component domino protocol for the microwave-assisted synthesis of functionalized naphtho[2,3-b]furan-4,9-diones in water
  195. CAN-promoted, diastereoselective synthesis of fused 2,3-dihydrofurans and their transformation into tetrahydroindoles
  196. ChemInform Abstract: Expedient, One-Pot Preparation of Fused Indoles via CAN-Catalyzed Three-Component Domino Sequences and Their Transformation into Polyheterocyclic Compounds Containing Pyrrolo[1,2-a]azepine Fragments.
  197. Environmental Effects on the Fluorescence of the Reaction Products of 2,3-Diphenylquinolizinium Bromide and Amines
  198. Half-Wave Potentials of 1-AZA- and 1,8-Diazaanthraquinones
  199. Corrigendum: Cover Picture: Discovery of a Class of Diketopiperazines as Antiprion Compounds (ChemMedChem 8/2010)
  200. Three-Component, Diastereoselective Synthesis of Highly Functionalized Indane Derivatives Based on an Anionic Domino Sequence from α-Nitroketones
  201. ChemInform Abstract: Cerium(IV) Ammonium Nitrate as a Catalyst in Organic Synthesis
  202. Cover Picture: Discovery of a Class of Diketopiperazines as Antiprion Compounds (ChemMedChem 8/2010)
  203. Synthesis of a Library of 5,6-Unsubstituted 1,4-Dihydropyridines Based on a One-Pot 4CR/Elimination Process and Their Application to the Generation of Structurally Diverse Fused Nitrogen Heterocycles
  204. ChemInform Abstract: Concise Synthesis of Tetrahydro Derivatives of the Pyrido[2,3-b]acridine and Pyrido[3,2-b]acridine Ring Systems.
  205. Discovery of a Class of Diketopiperazines as Antiprion Compounds
  206. ChemInform Abstract: Improvements in the Hetero Diels-Alder Reactions of 1-Dimethylamino-1-azadienes in the Presence of an Electrophilic Scavenger Resin.
  207. ChemInform Abstract: Hetero Diels-Alder Reactions of 1-Acetylamino- and 1-Dimethylamino-1-azadienes with Benzoquinones.
  208. ChemInform Abstract: A New Route Toward 4-Substituted Pyrazino[2,1-b]quinazoline-3,6-dione Systems. Total Synthesis of Glyantrypine.
  209. ChemInform Abstract: (o-Trifluoroacetamido)cinnamaldehyde Dimethylhydrazone, a Useful Azadiene in the Hetero Diels-Alder Approach to the Pyrido[2,3,4-kl]acridine System.
  210. ChemInform Abstract: Versatile Synthesis of Malonamic Acid Derivatives from a β-Ketothioester.
  211. ChemInform Abstract: L-Proline-Catalyzed Three-Component Domino [3 + 2 + 1] Annulation for the Regio- and Diastereoselective Synthesis of Highly Substituted Thienothiopyrans Containing Three or Four Stereocenters.
  212. ChemInform Abstract: Efficient Generation of Highly Functionalized Fused Oxazepine Frameworks Based on a CAN-Catalyzed Four-Component Tetrahydropyridine Synthesis/Ring-Closing Metathesis Sequence.
  213. Cerium(IV) Ammonium Nitrate as a Catalyst in Organic Synthesis
  214. ChemInform Abstract: Vinylation of Nitro-Substituted Indoles, Quinolinones, and Anilides with Grignard Reagents.
  215. ChemInform Abstract: A Mild Protocol for the Efficient Synthesis of 5,6-Unsubstituted 1,4-Dihydropyridines.
  216. ChemInform Abstract: Cerium(IV) Ammonium Nitrate Is an Excellent, General Catalyst for the Friedlaender and Friedlaender—Borsche Quinoline Syntheses: Very Efficient Access to the Antitumor Alkaloid Luotonin A.
  217. Concise and very efficient synthesis of the N-methylwelwistatin tetracyclic core based on an anionic domino process
  218. Expedient, one-pot preparation of fused indoles via CAN-catalyzed three-component domino sequences and their transformation into polyheterocyclic compounds containing pyrrolo[1,2-a]azepine fragments
  219. Multicomponent reactions for the synthesis of pyrroles
  220. ChemInform Abstract: Acid‐Free Synthesis of Carbazoles and Carbazolequinones by Intramolecular Pd‐Catalyzed, Microwave‐Assisted Oxidative Biaryl Coupling Reactions — Efficient Syntheses of Murrayafoline A, 2‐Methoxy‐3‐methylcarbazole, and Glycozolidine.
  221. l-Proline-Catalyzed Three-Component Domino [3+2+1] Annulation for the Regio- and Diastereoselective Synthesis of Highly Substituted Thienothiopyrans Containing Three or Four Stereocenters
  222. Mild and High-Yielding Synthesis of β-Keto Esters and β-Ketoamides
  223. Efficient Generation of Highly Functionalized Fused Oxazepine Frameworks Based on a CAN-Catalyzed Four-Component Tetrahydropyridine Synthesis/Ring-Closing Metathesis Sequence
  224. Vinylation of Nitro-Substituted Indoles, Quinolinones, and Anilides with Grignard Reagents
  225. Acid‐Free Synthesis of Carbazoles and Carbazolequinones by Intramolecular Pd‐Catalyzed, Microwave‐Assisted Oxidative Biaryl Coupling Reactions – Efficient Syntheses of Murrayafoline A, 2‐Methoxy‐3‐methylcarbazole, and Glycozolidine
  226. ChemInform Abstract: A Very Efficient Cerium(IV) Ammonium Nitrate Catalyzed, Four-Component Synthesis of Tetrahydropyridines and Its Application in the Concise Generation of Functionalized Homoquinolizine Frameworks.
  227. A Mild Protocol for the Efficient Synthesis of 5,6-Unsubstituted 1,4-Dihydropyridines
  228. ChemInform Abstract: New Synthetic Approaches to Biologically Relevant Heterocyclic Quinones and Quinoneimines
  229. ChemInform Abstract: Convenient, Two-Step Synthesis of 2-Styrylquinolines: An Application of the CAN-Catalyzed Vinylogous Type-II Povarov Reaction.
  230. Cerium(IV) Ammonium Nitrate Is an Excellent, General Catalyst for the Friedländer and Friedländer−Borsche Quinoline Syntheses: Very Efficient Access to the Antitumor Alkaloid Luotonin A
  231. A Very Efficient Cerium(IV) Ammonium Nitrate Catalyzed, Four-Component Synthesis of Tetrahydropyridines and Its Application in the Concise Generation of Functionalized Homoquinolizine Frameworks
  232. Convenient, two-step synthesis of 2-styrylquinolines: an application of the CAN-catalyzed vinylogous type-II Povarov reaction
  233. ChemInform Abstract: Stereoselective Synthesis of Bicyclo[4.2.1]nonanes - A Temporary-Bridge Approach to Cyclooctanoids.
  234. ChemInform Abstract: Two-Step Stereocontrolled Synthesis of Densely Functionalized Cyclic β-Aminoesters Containing Four Stereocenters, Based on a New Cerium(IV) Ammonium Nitrate Catalyzed Sequential Three-Component Reaction.
  235. Efficient, one-pot transformation of indoles into functionalized oxindole and spirooxindole systems under Swern conditions
  236. Stereoselective Synthesis of Bicyclo[4.2.1]nonanes - a Temporary-Bridge Approach to Cyclooctanoids
  237. ChemInform Abstract: Synthesis of Pyrido[3,2-b]carbazolequinones Involving N-Arylation of 5,8-Dimethoxy-6-nitroquinolines by Aryl Grignard Reagents and a New One-Pot, Palladium-Promoted Oxidative Coupling-Oxidative Demethylation Sequence.
  238. Two-Step Stereocontrolled Synthesis of Densely Functionalized Cyclic β-Aminoesters Containing Four Stereocenters, Based on a New Cerium(IV) Ammonium Nitrate Catalyzed Sequential Three-Component Reaction
  239. ChemInform Abstract: New Findings on the Cerium(IV) Ammonium Nitrate Catalyzed Povarov Reaction: Stereoselective Synthesis of 4-Alkoxy-2-aryl-1,2,3,4-tetrahydroquinoline Derivatives.
  240. Trends in the Design and Application of Optical Chemosensors in Pharmaceutical and Biomedical Analysis
  241. Synthesis of Pyrido[3,2-b]carbazolequinones Involving N-Arylation of 5,8-Dimethoxy-6-nitroquinolines by Aryl Grignard Reagents and a New One-Pot, Palladium-Promoted Oxidative Coupling-Oxidative Demethylation Sequence
  242. ChemInform Abstract: Microwave-Assisted, Solvent-Free Synthesis of Several Quinazoline Alkaloid Frameworks.
  243. ChemInform Abstract: One-Pot Synthesis of Highly Functionalized Oxindoles under Swern Oxidation Conditions.
  244. ChemInform Abstract: The Directed Lithiation Route to 2-Amino-3-alkylquinones: Highly Regioselective Introduction of Electrophiles at the C-7 Position of 2(1H)-Quinolinones.
  245. New Findings on the Cerium(IV) Ammonium Nitrate Catalyzed Povarov Reaction: Stereoselective Synthesis of 4-Alkoxy-2-aryl-1,2,3,4-tetrahydro­quinoline Derivatives
  246. DNA Alkylating Agents
  247. Introduction
  248. Cancer Chemoprevention
  249. Antimetabolites
  250. Preface
  251. DNA Intercalators and Topoisomerase Inhibitors
  252. Anticancer Drugs Targeting Tubulin and Microtubules
  253. Other Approaches to Targeted Therapy
  254. Drug Targeting in Anticancer Chemotherapy
  255. Drugs That Modulate Resistance to Antitumor Agents
  256. Anticancer Drugs That Inhibit Hormone Action
  257. Alkylating and Non-Alkylating Compounds Interacting with the DNA Minor Groove
  258. Drugs That Inhibit Signalling Pathways for Tumor Cell Growth and Proliferation
  259. Anticancer Drugs Acting via Radical Species, Photosensitizers and Photodynamic Therapy of Cancer
  260. Medicinal Chemistry of Anticancer Drugs
  261. Convenient Synthesis of Highly Functionalized, 3,4-Disubstituted Indole Building Blocks
  262. Convenient Synthesis of Highly Functionalized, 3,4-Disubstituted Indole Building Blocks
  263. Microwave-Assisted, Solvent-Free Synthesis of Several Quinazoline Alkaloid Frameworks
  264. One-Pot Synthesis of Highly Functionalized Oxindoles under Swern Oxidation Conditions
  265. The Directed Lithiation Route to 2-Amino-3-alkylquinones: Highly Regioselective Introduction of Electrophiles at the C-7 Position of 2(1H)-Quinolinones
  266. The First Aza Diels—Alder Reaction Involving an α,β-Unsaturated Hydrazone as the Dienophile: Stereoselective Synthesis of C-4 Functionalized 1,2,3,4-Tetrahydroquinolines Containing a Quaternary Stereocenter.
  267. Peptidomimetics in cancer chemotherapy
  268. A New Three-Component Domino Synthesis of 1,4-Dihydropyridines.
  269. CAN-Catalyzed Vinylogous Povarov Reactions: The First Three-Component Synthesis of 2-Functionalized Tetrahydroquinolines from Anilines, Cinnamaldehyde and Vinyl Ethers.
  270. General, Mild and Efficient Synthesis of β-Enaminones Catalyzed by Ceric Ammonium Nitrate.
  271. CAN-Catalyzed Three-Component Reaction Between Anilines and Alkyl Vinyl Ethers: Stereoselective Synthesis of 2-Methyl-1,2,3,4-tetrahydroquinolines and Studies on Their Aromatization.
  272. A new three-component domino synthesis of 1,4-dihydropyridines
  273. CAN-Catalyzed Vinylogous Povarov Reactions: The First Three-Component Synthesis of 2-Functionalized Tetrahydroquinolines from Anilines, ­Cinnamaldehyde and Vinyl Ethers
  274. General, Mild and Efficient Synthesis of β-Enaminones Catalyzed by Ceric Ammonium Nitrate
  275. Changes in the reactivity of the fluorescent reagents carbazole-9-carbonyl chloride and 9-carbazolylacetic acid in the presence of cyclodextrins
  276. Synthesis of Oxygenated Carbazoles by Palladium‐Mediated Oxidative Double C—H Activation of Diarylamines Assisted by Microwave Irradiation.
  277. The first aza Diels–Alder reaction involving an α,β-unsaturated hydrazone as the dienophile: stereoselective synthesis of C-4 functionalized 1,2,3,4-tetrahydroquinolines containing a quaternary stereocenter
  278. CAN-catalyzed three-component reaction between anilines and alkyl vinyl ethers: stereoselective synthesis of 2-methyl-1,2,3,4-tetrahydroquinolines and studies on their aromatization
  279. Structural Studies on Heterocyclic Quinones and Quinonimines
  280. Synthesis of Oxygenated Carbazoles by Palladium-Mediated Oxidative Double C-H Activation of Diarylamines Assisted by Microwave Irradiation
  281. Efficient Synthesis of N -Prenylpyrroloindoline and N -Prenylindole Alkaloids Based on a New Four-Reaction Anionic Domino Process
  282. Multicomponent Reactions
  283. MDR Reversal by Deprenylated Tetracyclic and Hexacyclic Analogues of N-Acetylardeemin: Confirmation of the Ardeemin Pharmacophore
  284. Microwave-Assisted, Solvent-Free Bischler Indole Synthesis.
  285. Microwave-Assisted Synthesis of 2,5-Piperazinediones under Solvent-Free Conditions.
  286. Microwave Assisted Organic Synthesis
  287. Microwave-Assisted, Solvent-Free Bischler Indole Synthesis
  288. Solvent-Free, Efficient Synthesis of 2,5-Piperazinediones from Boc-Protected Dipeptide Esters under Microwave Irradiation.
  289. An Efficient Procedure for the Deprotection of N-Pivaloylindoles, Carbazoles and β-Carbolines with LDA.
  290. Environmental effects on the fluorescence behaviour of carbazole derivatization reagents
  291. Unique Michael Addition-Initiated Domino Reaction for the Stereoselective Synthesis of Functionalized Macrolactones from α-Nitroketones in Water
  292. Microwave-Assisted Synthesis of 2,5-Piperazinediones under Solvent-Free Conditions
  293. An Efficient Procedure for the Deprotection of N -Pivaloylindoles, Carbazoles and β-Carbolines with LDA
  294. Solvent-Free, Efficient Synthesis of 2,5-Piperazinediones from Boc-Protected Dipeptide Esters under Microwave Irradiation
  295. Synthetic Studies on N-Methylwelwitindolinone C Isothiocyanate (Welwistatin) and Related Substructures
  296. Stereoselective Synthesis of Bicyclo[4.2.1]nonane Skeletons by Ring-Closing Metathesis: A New Versatile Methodology for the Efficient Assembly of Functionalized Cyclooctanoids.
  297. Synthesis and Structure—Activity Relationships of 1,5-Diazaanthraquinones as Antitumor Compounds.
  298. Synthesis and biological evaluation of new 1,5-diazaanthraquinones with cytotoxic activity
  299. Solvent-Free Cyclocondensation of Lactim Ethers with Anthranilic Acid under Microwave Irradiation.
  300. Stereoselective Synthesis of Bicyclo[4.2.1]nonane Skeletons by Ring-Closing Metathesis:  A New Versatile Methodology for the Efficient Assembly of Functionalized Cyclooctanoids
  301. Synthesis and structure–activity relationships of 1,5-diazaanthraquinones as antitumour compounds
  302. Practical and User-Friendly Procedure for Michael Reactions of α-Nitroketones in Water.
  303. Brief Total Synthesis of the Cell Cycle Inhibitor Tryprostatin B (I) and Related Preparation of Its Alanine Analogue (II).
  304. Solvent-Free Cyclocondensation of Lactim Ethers with Anthranilic Acid under Microwave Irradiation
  305. Synthetic Studies on N-Methylwelwitindolinone C Isothiocyanate (Welwistatin) and Related Substructures
  306. Regioselective Diels-Alder Reactions of 3-Vinylindoles with Quinones
  307. Efficient Synthesis of the Pyrido[2,3,4-kl]acridin-4-one System Common to Several Cytotoxic Marine Alkaloids.
  308. Brief Total Synthesis of the Cell Cycle Inhibitor Tryprostatin B and Related Preparation of Its Alanine Analogue
  309. Regioselective Diels—Alder Reactions of 3-Indolylquinones.
  310. Detection and characterization of cyclodextrin complexes with β-carboline derivatives by spectroscopic techniques
  311. Efficient synthesis of the pyrido[2,3,4-kl]acridin-4-one system common to several cytotoxic marine alkaloids
  312. Chemistry of Pyrazino[2,1-b]quinazoline-3,6-diones
  313. Regioselective Diels–Alder reactions of 3-indolylquinones
  314. Efficient, Multigram-Scale Synthesis of Three 2,5-Dihalobenzoquinones
  315. Practical and User-Friendly Procedure for Michael Reactions of α-Nitro­ketones in Water
  316. Chemistry of Pyrazino[2,1-b]quinazoline-3,6-diones
  317. Differentiating geometrical isomers of retinoids and controlling their photo-isomerization by complexation with cyclodextrins
  318. EFFICIENT, MULTIGRAM-SCALE SYNTHESIS OF THREE 2,5-DIHALOBENZOQUINONES
  319. Inhibitors of Multidrug Resistance to Antitumor Agents (MDR)
  320. One-pot assembly of large heterocyclic quinones through three-component reactions
  321. Versatile synthesis of malonamic acid derivatives from a β-ketothioester
  322. A C-Ring Regioisomer of the Marine Alkaloid Meridine Exhibits Selective In Vitro Cytotoxicity for Solid Tumours
  323. Hydantoin and Its Derivatives
  324. ChemInform Abstract: Concise Preparation of 1,8-Diazaanthracene-2,7,9,10-tetraones. Two Alternative Syntheses of the Natural Antifolate Diazaquinomycin A.
  325. Concise Preparation of 1,8-Diazaanthracene-2,7,9,10-Tetraones. Two Alternative Syntheses of the Natural Antifolate Diazaquinomycin A
  326. Hetero Diels–Alder Reactions of 1-Acetylamino- and 1-Dimethylamino-1-azadienes with Benzoquinones
  327. A New Route toward 4-Substituted Pyrazino[2,1-b]quinazoline-3,6-dione Systems. Total Synthesis of Glyantrypine
  328. Improvements in the Hetero Diels-Alder Reactions of 1-Dimethylamino-1-azadienes in the Presence of an Electrophilic Scavenger Resin
  329. Synthesis of a Seco Analogue of Ardeemin
  330. ELECTROCHEMICAL EVIDENCE FOR OXO-ENOL TAUTOMERISM OF AZAANTHRACENE-4,9,10-TRIONES
  331. Steric and stereochemical effects on the free-radical bromination of tetracyclic and hexacyclic fragments of the MDR inhibitor N-acetylardeemin
  332. Concise synthesis of tetrahydro derivatives of the pyrido[2,3-b]acridine and pyrido[3,2-b]acridine ring systems
  333. Synthesis of 1,2,3,4-tetrahydroascididemin
  334. Quantitative determination of dimethicone in commercial tablets and capsules by Fourier transform infrared spectroscopy and antifoaming activity test
  335. Comparative study of synthetic approaches to 1-arylmethylenepyrazino[2,1-b]quinazoline-3,6-diones
  336. On the fate of the tryptophan stereocenter during the synthesis of hexacyclic analogues of N-acetylardeemin
  337. Stereochemical issues related to the synthesis and reactivity of pyrazino[2′,1′-5,1]pyrrolo[2,3-b]indole-1,4-diones
  338. A General Synthesis of Quinoline-2,5,8(1H)-triones via Acylation of 2,5-Dimethoxyaniline with S-tert-Butyl Thioacetates by Application of the Knorr Cyclization
  339. Total synthesis of diazaquinomycin A
  340. Hetero Diels-Alder reactions of 4,5,8(1H)-quinolinetriones
  341. A very efficient synthesis of 1,8-diazaanthraquinones
  342. 1,2-Dihydroquinolin-2-one (carbostyril) anions as bidentate nucleophiles in their reactions with aryllead triacetates: synthesis of 1-aryl- and 3-aryl-tetrahydroquinoline-2,5,8-triones
  343. Silica gel-supported hetero Diels-Alder reactions of quinolinetriones
  344. Analytical applications of retinoid—cyclodextrin inclusion complexes
  345. New findings in hetero Diels-Alder reactions of quinolinetriones
  346. Bicyclic 6-6 Systems with One Ring Junction Nitrogen Atom: No Extra Heteroatom
  347. New Synthetic Applications of Aryllead Triacetates. N-Arylation of Amides
  348. New synthetic applications of aryllead triacetates. N-arylation of azoles.
  349. 1-Acylamino-1-azadienes as an alternative to 1-dimethylamino-1-azadienes in the preparation of 1,8-diazaanthracene-2,9,10-triones.
  350. Solvent effects on the fluorescent emission of some new benzimidazole derivatives
  351. Regioselectivity of the Diels-Alder reactions of 2,5,8(1H)-quinolinetriones
  352. Ultrasound assisted Diels-Alder reactions of 1-azadienes with “normal” electronic demand.
  353. Re-examination of the Synthesis of 3,5-Dimethoxy-2-nitrobenzaldehyde
  354. New findings on the Vilsmeier-Haack approach to quinoline derivatives
  355. Amide N-arylation with p-tolyllead triacetate
  356. An Improved Multigram-Scale Preparation ofS-TertButyl Acetothioacetate
  357. N-arylation of azoles and their benzo derivatives by p-tolyllead triacetate
  358. Synthesis, anticonvulsant and antihypertensive activity of diastereomeric 9,10-dimethoxy-1,3,4,6,7,11b-hexahydrospiro-[benzo[a]quinolizin-2,4′-imidazolidine]-2′,5′-diones
  359. Total Synthesis of the Carboxylic Acid lonophore Antibiotic CP-61,405 (Routiennocin): Preparation of the Inherent Spiroketal Unit via a Reverse Coupling Process
  360. Total synthesis of the ionophore antibiotic CP-61,405 (routiennocin)
  361. Synthesis of 1′-substituted and 1′,3′-disubstituted (±)-2R*, 11bS*-9,10-Dimethoxy-1,3,4,6,7,11 b-Hexahydrospiro-[benzo[a]quinolizin-2,5′-imidazolidine]-2′,4′-diones
  362. Study of the Reaction Between Cyanohydrins and Chlorosulfonyl Isocyanate. A New, Efficient Method for the One-Pot Synthesis of 2,4-Oxazolidinediones
  363. The application of ultrasound to the strecker synthesis on 9,10-dimethoxy-1,3,4,6,7,11b-hexahydrobenzo[a]quinolizin-2-one
  364. Chemistry of the Welwitindolinones