All Stories

  1. ChemInform Abstract: Chopping Unfunctionalized Carbon—Carbon Bonds: a New Paradigm for the Synthesis of Organonitriles
  2. Copper-Mediated Cross-Coupling Reactions. Editors: Gwilherm Evano and Nicolas Blanchard
  3. ChemInform Abstract: Practical Methods for the Synthesis of Trifluoromethylated Alkynes: Oxidative Trifluoromethylation of Copper Acetylides and Alkynes.
  4. Synthetic Variants of Mycolactone Bind and Activate Wiskott–Aldrich Syndrome Proteins
  5. Copper‐Mediated Cross‐Coupling Reactions. Herausgegeben von Gwilherm Evano und Nicolas Blanchard.
  6. Copper-Mediated Cross-Coupling Reactions. Edited by Gwilherm Evano and Nicolas Blanchard.
  7. Practical Methods for the Synthesis of Trifluoromethylated Alkynes: Oxidative Trifluoromethylation of Copper Acetylides and Alkynes
  8. On the Synthesis, Characterization and Reactivity of N-Heteroaryl-Boryl Radicals, a New Radical Class Based on Five-Membered Ring Ligands
  9. Chopping unfunctionalized carbon–carbon bonds: a new paradigm for the synthesis of organonitriles
  10. Formation of N-Heterocyclic Carbene–Boryl Radicals through Electrochemical and Photochemical Cleavage of the B–S bond in N-Heterocyclic Carbene–Boryl Sulfides
  11. Copper‐Mediated Cross‐Coupling Reactions
  12. Copper‐Catalyzed C–C Bond Formation in Natural Product Synthesis: Elegant and Efficient Solutions to a Key Bond Disconnection
  13. ChemInform Abstract: Taming Sulfur Dioxide: A Breakthrough for Its Wide Utilization in Chemistry and Biology
  14. Mechanistic and Preparative Studies of Radical Chain Homolytic Substitution Reactions of N-Heterocyclic Carbene Boranes and Disulfides
  15. BODIPY derivatives and boranil as new photoinitiating systems of cationic polymerization exhibiting a tunable absorption in the 400–600 nm spectral range
  16. History, biology and chemistry of Mycobacterium ulcerans infections (Buruli ulcer disease)
  17. Taming sulfur dioxide: a breakthrough for its wide utilization in chemistry and biology
  18. Soft Photopolymerizations Initiated by Dye-Sensitized Formation of NHC-Boryl Radicals under Visible Light
  19. Photopolymerization of Cationic Monomers and Acrylate/Divinylether Blends under Visible Light Using Pyrromethene Dyes
  20. Photoredox Catalysis for Polymerization Reactions
  21. Tunable Organophotocatalysts for Polymerization Reactions Under Visible Lights.
  22. Iridium Photocatalysts in Free Radical Photopolymerization under Visible Lights
  23. ChemInform Abstract: Synthesis of Spiroketals under Neutral Conditions via a Type III Ring‐Rearrangement Metathesis Strategy.
  24. Organic Photocatalyst for Polymerization Reactions: 9,10-Bis[(triisopropylsilyl)ethynyl]anthracene
  25. Cover Picture: A Diverted Total Synthesis of Mycolactone Analogues: An Insight into Buruli Ulcer Toxins (Chem. Eur. J. 51/2011)
  26. Ruthenium-catalyzed [2+2] cycloaddition reactions of a 2-oxa-3-azabicyclo[2.2.1]hept-5-ene with unsymmetrical alkynes
  27. A Diverted Total Synthesis of Mycolactone Analogues: An Insight into Buruli Ulcer Toxins
  28. Subtle Ligand Effects in Oxidative Photocatalysis with Iridium Complexes: Application to Photopolymerization
  29. Household LED irradiation under air: cationic polymerization using iridium or ruthenium complex photocatalysts
  30. A Novel Photopolymerization Initiating System Based on an Iridium Complex Photocatalyst
  31. Decatungstate (W10O 324−)/Silane: A New and Promising Radical Source Under Soft Light Irradiation
  32. ChemInform Abstract: Synthesis of Natural Products Containing Medium‐Size Carbocycles by Ring‐Closing Alkene Metathesis
  33. Tandem cationic and sol-gel photopolymerizations of a vinyl ether alkoxysilane
  34. Silyloxyamines as sources of silyl radicals: ESR spin‐trapping, laser flash photolysis investigation, and photopolymerization ability
  35. An Approach Toward Homocalystegines and Silyl-homocalystegines. Acid-Mediated Migrations of Acetates in Seven-Membered Ring Systems
  36. Synthesis of spiroketals under neutral conditions via a type III ring-rearrangement metathesis strategy
  37. Controlled synthesis of branched poly(vinyl acetate)s by xanthate-mediated RAFT self-condensing vinyl (co)polymerization
  38. New thioxanthone and xanthone photoinitiators based on silyl radical chemistry
  39. Efficient dual radical/cationic photoinitiator under visible light: a new concept
  40. Green Bulb Light Source Induced Epoxy Cationic Polymerization under Air Using Tris(2,2′-bipyridine)ruthenium(II) and Silyl Radicals
  41. Near UV–visible light induced cationic photopolymerization reactions: A three component photoinitiating system based on acridinedione/silane/iodonium salt
  42. New Boryl Radicals Derived from N‐Heteroaryl Boranes: Generation and Reactivity
  43. ChemInform Abstract: Diastereoselective Hydroboration of Isopropenylcyclopropanes.
  44. ChemInform Abstract: Stereoselective Synthesis of Cyclopropanes Bearing Adjacent Stereocenters.
  45. Synthesis of Natural Products Containing Medium‐Size Carbocycles by Ring‐Closing Alkene Metathesis
  46. α-Acyloxynitroso dienophiles in [4+2] hetero Diels–Alder cycloadditions: mechanistic insights
  47. Bis(germyl)ketones: Toward a New Class of Type I Photoinitiating Systems Sensitive Above 500 nm?
  48. ChemInform Abstract: Rhodium-Catalyzed Ring-Opening Reactions of a 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene with Arylboronic Acids.
  49. ChemInform Abstract: Ruthenium‐Catalyzed Nucleophilic Ring‐Opening Reactions of a 3‐Aza‐2‐oxabicyclo[2.2.1]hept‐5‐ene with Alcohols.
  50. Rhodium-Catalyzed Ring-Opening Reactions of a 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene with Arylboronic Acids
  51. Effect of Lewis base coordination on boryl radical reactivity: investigation using laser flash photolysis and kinetic ESR
  52. Ruthenium-Catalyzed Nucleophilic Ring-Opening Reactions of a 3-Aza-2-oxabicyclo[2.2.1]hept-5-ene with Alcohols
  53. ChemInform Abstract: Copper‐Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis
  54. Tris(trimethylsilyl)silyl versus tris(trimethylsilyl)germyl: Radical reactivity and oxidation ability
  55. ChemInform Abstract: Efficient Cleavage of the N-O Bond of 3,6-Dihydro-1,2-oxazines Mediated by Some α-Hetero Substituted Carbonyl Compounds in Mild Conditions.
  56. Copper-Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis
  57. Efficient cleavage of the N–O bond of 3,6-dihydro-1,2-oxazines mediated by some α-hetero substituted carbonyl compounds in mild conditions
  58. Domino Metathesis of 3,6‐Dihydro‐1,2‐oxazine: Access to Isoxazolo[2,3‐a]pyridin‐7‐ones.
  59. 2,2-Dimethyl-5-nitroso-1,3-dioxan-5-yl benzoate, 2,2-dimethyl-5-nitroso-1,3-dioxan-5-yl 4-chlorobenzoate and 5-nitroso-1,3-dioxan-5-yl 4-chlorobenzoate
  60. Metathesis of Heteroatom‐Substituted Olefins and Alkynes: Current Scope and Limitations.
  61. Domino Metathesis of 3,6-Dihydro-1,2-oxazine:  Access to Isoxazolo[2,3-a]pyridin-7-ones
  62. Metathesis of heteroatom-substituted olefins and alkynes: Current scope and limitations
  63. Daucus carota L. Mediated Bioreduction of Prochiral Ketones
  64. Synthesis of Polysubstituted Pyrroles from Nitroso-Diels—Alder Cycloadducts.
  65. Intermolecular Nitroso Diels—Alder Cycloaddition of α‐Acetoxynitroso Derivatives in Aqueous Medium.
  66. Daucus carota L. mediated bioreduction of prochiral ketones
  67. Total Synthesis of Zincophorin and Its Methyl Ester
  68. Synthesis of polypropionate subunits from cyclopropanes
  69. Intermolecular nitroso Diels–Alder cycloaddition of α-acetoxynitroso derivatives in aqueous medium
  70. Total synthesis of zincophorin
  71. Synthesis of Polysubstituted Pyrroles from Nitroso-Diels-Alder Cycloadducts
  72. Total Synthesis of Formamicin.
  73. Lewis Acid Promoted Hetero Diels—Alder Cycloaddition of α‐Acetoxynitroso Dienophiles.
  74. Total Synthesis of Formamicin
  75. Lewis Acid-Promoted Hetero Diels−Alder Cycloaddition of α-Acetoxynitroso Dienophiles
  76. Total Synthesis of Zincophorin and Its Methyl Ester
  77. Total Synthesis of Zincophorin Methyl Ester.
  78. Stereoselective Synthesis of Polypropionate Units and Heterocyclic Compounds by Cyclopropylcarbinol Ring-Opening with Mercury(II) Salts
  79. Chapter 10 Total synthesis of zincophorin and its methyl ester
  80. Total Synthesis of Zincophorin Methyl Ester
  81. Stereoselective Synthesis of Polypropionate Units and Heterocyclic Compounds by Cyclopropylcarbinol Ring-Opening with Mercury(II) Salts
  82. Total Synthesis of the Formamicin Aglycon, Formamicinone.
  83. Total Synthesis of the Formamicin Aglycon, Formamicinone
  84. 2-Deoxy-2-iodo-β-glucopyranosyl Fluorides:  Mild and Highly Stereoselective Glycosyl Donors for the Synthesis of 2-Deoxy-β-glycosides from β-Hydroxy Ketones
  85. A Synthetic Approach Towards the C1—C9 Subunit of Zincophorin.
  86. ChemInform Abstract: Stereoselective Oxymercuration of Cyclopropylcarbinols with Anchimeric Assistance by Aromatic Groups.
  87. A Synthetic Approach towards the C1–C9 Subunit of Zincophorin
  88. A Synthetic Approach towards the C1–C9 Subunit of Zincophorin
  89. ChemInform Abstract: Synthesis of Isopropenylcyclopropanes — Revision of the Relative Configuration of Cyclopropyl Ketones Obtained by 1,3‐Elimination of γ‐Epoxy Ketones.
  90. Stereoselective oxymercuration of cyclopropylcarbinols with anchimeric assistance by aromatic groups
  91. ChemInform Abstract: Synthesis of Stereotriads by Oxymercuration of Substituted Cyclopropylcarbinols.
  92. Synthesis of Stereotriads by Oxymercuration of Substituted Cyclopropylcarbinols
  93. Synthesis of Isopropenylcyclopropanes − Revision of the Relative Configuration of Cyclopropyl Ketones Obtained by 1,3-Elimination of γ-Epoxy Ketones
  94. Synthesis of Isopropenylcyclopropanes − Revision of the Relative Configuration of Cyclopropyl Ketones Obtained by 1,3-Elimination of γ-Epoxy Ketones
  95. ChemInform Abstract: Diastereoselectivity in the Dihydroxylation of Isopropenyl‐Substituted Three‐Membered Rings.
  96. Diastereoselectivity in the dihydroxylation of isopropenyl substituted three-membered rings
  97. Diastereoselective Hydroboration of Isopropenylcyclopropanes
  98. Directing Effect of a Neighboring Aromatic Group in the Cyclopropanation of Allylic Alcohols