All Stories

  1. ChemInform Abstract: Catalytic Asymmetric Bromolactonization Reactions Using (DHQD)2PHAL‐Benzoic Acid Combinations.
  2. Fabrication of hybrid polymer/metal organic framework membranes: mixed matrix membranes versus in situ growth
  3. Proof-of-principle direct double cyclisation of a linear C15-precursor to a dibrominated bicyclic medium-ring ether relevant toLaurenciaspecies
  4. Studies towards the synthesis of halomon: asymmetric hexafunctionalisation of myrcene
  5. Catalytic asymmetric bromolactonization reactions using (DHQD)2PHAL-benzoic acid combinations
  6. An Enantiospecific Polyene Cyclization Initiated by an Enantiomerically Pure Bromonium Ion
  7. Epoxidation of bromoallenes connects red algae metabolites by an intersecting bromoallene oxide – Favorskii manifold
  8. A Unifying Stereochemical Analysis for the Formation of Halogenated C15-Acetogenin Medium-Ring Ethers From Laurencia Species via Intramolecular Bromonium Ion Assisted Epoxide Ring-Opening and Experimental Corroboration with a Model Ep...
  9. Verification of stereospecific dyotropic racemisation of enantiopure d and l-1,2-dibromo-1,2-diphenylethane in non-polar media
  10. ChemInform Abstract: Enantiospecific Bromonium Ion Generation and Intramolecular Capture: A Model System for Asymmetric Bromonium Ion‐Induced Polyene Cyclizations.
  11. Total Synthesis of the Marine Metabolite (±)-Polysiphenol via Highly Regioselective Intramolecular Oxidative Coupling
  12. ChemInform Abstract: The Reaction of Aromatic Dialdehydes with Enantiopure 1,2‐Diamines: An Expeditious Route to Enantiopure Tricyclic Amidines.
  13. Enantiospecific bromonium ion generation and intramolecular capture: a model system for asymmetric bromonium ion-induced polyene cyclisations
  14. The reaction of aromatic dialdehydes with enantiopure 1,2-diamines: an expeditious route to enantiopure tricyclic amidines
  15. Intramolecular Bromonium Ion Assisted Epoxide Ring-Opening: Capture of the Oxonium Ion with an Added External Nucleophile
  16. Correction to Clarification of the Stereochemical Course of Nucleophilic Substitution of Arylsulfonate-Based Nucleophile Assisting Leaving Groups
  17. Clarification of the Stereochemical Course of Nucleophilic Substitution of Arylsulfonate-Based Nucleophile Assisting Leaving Groups
  18. ChemInform Abstract: Bromonium Ion Induced Transannular Oxonium Ion Formation—Fragmentation in Model Obtusallene Systems and Structural Reassignment of Obtusallenes V—VII.
  19. ChemInform Abstract: The Generation and Trapping of Enantiopure Bromonium Ions.
  20. Bromonium Ion Induced Transannular Oxonium Ion Formation−Fragmentation in Model Obtusallene Systems and Structural Reassignment of Obtusallenes V−VII
  21. The generation and trapping of enantiopure bromonium ions
  22. ChemInform Abstract: The Stereochemical Course of Bromoetherification of Enynes.
  23. Structural Reassignment of Obtusallenes V, VI, and VII by GIAO-Based Density Functional Prediction
  24. The stereochemical course of bromoetherification of enynes
  25. Amidines as Potent Nucleophilic Organocatalysts for the Transfer of Electrophilic Bromine from N‐Bromosuccinimide to Alkenes.
  26. Amidines as potent nucleophilic organocatalysts for the transfer of electrophilic bromine from N-bromosuccinimide to alkenes
  27. Vacuum-driven anionic ligand exchange in Buchmeiser–Hoveyda–Grubbs ruthenium(II) benzylidenes
  28. Dimethylformamide, Dimethylacetamide and Tetramethylguanidine as Nucleophilic Organocatalysts for the Transfer of Electrophilic Bromine from N‐Bromosuccinimide to Alkenes.
  29. Dimethylformamide, dimethylacetamide and tetramethylguanidine as nucleophilic organocatalysts for the transfer of electrophilic bromine from N-bromosuccinimide to alkenes
  30. A Biosynthetically-Inspired Synthesis of the Tetrahydrofuran Core of Obtusallenes II and IV
  31. A Hypothesis Concerning the Biosynthesis of the Obtusallene Family of Marine Natural Products via Electrophilic Bromination
  32. Fractional crystallisation of (±)-iso-amarine with mandelic acid: convenient access to (R,R)- and (S,S)-1,2-diamino-1,2-diphenylethanes
  33. Anionic Ligand Exchange in Hoveyda−Grubbs Ruthenium(II) Benzylidenes
  34. ortho‐Substituted Iodobenzenes as Novel Organocatalysts for Bromination of Alkenes.
  35. Bromoiodinanes with an I(III)—Br Bond: Preparation, X‐Ray Crystallography and Reactivity as Electrophilic Brominating Agents.
  36. A Convenient Preparation of Enantiomerically Pure (+)‐(1R,2R)‐ and (−)‐(1S,2S)‐1,2‐Diamino‐1,2‐diphenylethanes
  37. Ortho-substituted iodobenzenes as novel organocatalysts for bromination of alkenes
  38. Bromoiodinanes with an I(iii)–Br bond: preparation, X-ray crystallography and reactivity as electrophilic brominating agents
  39. Tris[(perfluoroalkyl)sulfonyl]methanes and Related Salts
  40. A general synthesis of five, six and seven-membered silasultones via dehydrative cyclisation
  41. Oxidation and Reduction
  42. A convenient synthesis of high-loaded palladium(II) ROMP polymers
  43. A Silicon-Centred Tetrafunctionalised Reagent for the Cyclopropylmethylsilane-Terminated Prins Reaction and a Concise Synthesis of Lyngbic Acid
  44. An asymmetric synthesis of enantiopure chair and twist trans-cyclooctene isomers
  45. Planar Chiral PHANOLs as Double Hydrogen Bonding Donor Organocatalysts: Synthesis and Catalysis
  46. A preparative microwave method for the isomerisation of 4,16-dibromo[2.2]paracyclophane into 4,12-dibromo[2.2]paracyclophane
  47. (Diacetoxyiodo)benzene—Lithium Bromide as a Convenient Electrophilic Br+ Source.
  48. Tris[(trifluoromethyl)sulfonyl]methane and Related Salts
  49. (Diacetoxyiodo)benzene-Lithium Bromide as a Convenient Electrophilic Br + Source
  50. Planar Chiral PHANOLs as Organocatalysts for the Diels—Alder Reaction via Double Hydrogen‐Bonding to a Carbonyl Group.
  51. The Cyclopropylmethylsilane Terminated Prins Reaction: Stereoelectronic Controlled Formation of (E)‐Skipped Dienes Alcohols and a (Z)‐Skipped Diene Modification.
  52. A Highly Active Ytterbium(III) Methide Complex for Truly Catalytic Friedel—Crafts Acylation Reactions.
  53. Planar Chiral PHANOLs as Organocatalystsfor the Diels-Alder Reaction via Double Hydrogen-Bondingto a Carbonyl Group
  54. The Cyclopropylmethylsilane Terminated Prins Reaction: Stereoelectronic Controlled Formation of ( E )-Skipped Dienes Alcohols and a ( Z )-Skipped Diene Modification
  55. Improved Synthesis of (±)-4,12-Dihydroxy[2.2]paracyclophane and Its Enantiomeric Resolution by Enzymatic Methods:  Planar Chiral (R)- and (S)-Phanol
  56. Application of lanthanide catalysis in the penicillin to cephalosporin conversion
  57. ChemInform Abstract: In situ Tandem Allylic Acetate Isomerization‐Ring Closing Metathesis: 1,3‐Dimesityl‐4,5‐dihydroimidazol‐2‐ylidene Ruthenium Benzylidenes and Palladium(0)—Phosphine Combinations.
  58. ChemInform Abstract: 5,10,15,20‐Tetraphenylporphyrinatorhodium(III) Iodide Catalyzed Cyclopropanation Reactions of Alkenes Using Glycine Ester Hydrochloride.
  59. Synthesis of some ytterbium(III) tris-(perfluoroalkylsulfonyl)methides
  60. Bis(tricyclohexylphosphine)(4-polystyrylmethylidene)ruthenium Dichloride
  61. ChemInform Abstract: The Cyclopropylmethylsilane Terminated Prins Reaction: Stereoelectronic Controlled Formation of (E)‐Skipped Dienes.
  62. A Highly Active Ytterbium(III) Methide Complex for Truly Catalytic Friedel-Crafts Acylation Reactions
  63. 5,10,15,20-Tetraphenylporphyrinatorhodium(III) Iodide Catalyzed Cyclopropanation Reactions of Alkenes Using Glycine Ester Hydrochloride
  64. ChemInform Abstract: Asymmetric Synthesis and Lewis Acid Mediated Type II Carbonyl Ene Cyclizations of (R)‐2‐Isopropyl‐5‐methylhex‐5‐enal.
  65. ChemInform Abstract: Asymmetric Allylboration and Ring Closing Alkene Metathesis: A Novel Strategy for the Synthesis of Glycosphingolipids.
  66. Award
  67. The Cyclopropylmethylsilane Terminated Prins Reaction: Stereoelectronic Controlled Formation of (E)-Skipped Dienes
  68. ChemInform Abstract: Second Generation Recyclable “Boomerang” Polymer‐Supported Catalysts for Olefin Metathesis: Application of Arduengo Carbene Complexes.
  69. ChemInform Abstract: Tandem Ireland—Claisen Rearrangement Ring‐Closing Alkene Metathesis in the Construction of Bicyclic β‐Lactam Carboxylic Esters.
  70. ChemInform Abstract: Fluorous Biphase Catalytic Friedel—Crafts Acylation: Ytterbium Tris(Perfluoroalkanesulfonyl)methide Catalysts.
  71. ChemInform Abstract: Catalytic and Stoichiometric Lewis Acid Participation in Aldehyde Ene Cyclizations.
  72. Asymmetric Allylboration and Ring Closing Alkene Metathesis:  A Novel Strategy for the Synthesis of Glycosphingolipids
  73. ChemInform Abstract: Allene Cross‐Metathesis: Synthesis of 1,3‐Disubstituted Allenes.
  74. Tandem Ireland−Claisen Rearrangement Ring-Closing Alkene Metathesis in the Construction of Bicyclic β-Lactam Carboxylic Esters
  75. ChemInform Abstract: A Recyclable “Boomerang” Polymer‐Supported Ruthenium Catalyst for Olefin Metathesis.
  76. Allene Cross-Metathesis: Synthesis of 1,3-Disubstituted Allenes
  77. Bidirectional Asymmetric Allylboration. A Convenient Asymmetric Synthesis of C2-Symmetric 3-Methylenepentane-1,5-diols and Rapid Access to C2-Symmetric Spiroketals
  78. ChemInform Abstract: Ytterbium(III) Triflate as a Recyclable Catalyst for the Selective Atom Economic Oxidation of Benzyl Alcohols to Benzaldehydes.
  79. Ytterbium(III) Triflate as a Recyclable Catalyst for the Selective Atom Economic Oxidation of Benzyl Alcohols to Benzaldehydes
  80. ChemInform Abstract: Ytterbium(III) Triflate‐Catalyzed Preparation of Calix[4]resorcinarenes: Lewis Assisted Broensted Acidity.
  81. ChemInform Abstract: A Tripartite Asymmetric Allylboration — Silicon Tethered Alkene Ring Closing Metathesis — in situ Ring Opening Protocol for the Regiospecific Generation of Functionalized (E)‐Disubstituted Homoallylic Alcohols.
  82. ChemInform Abstract: Lanthanoid(III) and Group IV Metal Triflate Catalyzed Electrophilic Nitration: ′Nitrate Capture′ and the Role of the Metal Centre
  83. ChemInform Abstract: Bidirectional Asymmetric Allylboration and the Synthesis of C2 Symmetric 3‐Methylenepentane‐1,5‐diols.
  84. ChemInform Abstract: Rapid Entry into Mono‐, Bi‐, and Tricyclic β‐Lactam Arrays via Alkene Metathesis.
  85. Tris(trifluoromethanesulfonyl)methide (“Triflide”) Anion:  Convenient Preparation, X-ray Crystal Structures, and Exceptional Catalytic Activity as a Counterion with Ytterbium(III) and Scandium(III)
  86. A tripartite asymmetric allylboration ? Silicon tethered alkene ring closing metathesis ? in situ ring opening protocol for the regiospecific generation of functionalized (E)-disubstituted homoallylic alcohols
  87. Bidirectional asymmetric allylboration and the synthesis of C2 symmetric 3-methylenepentane-1,5-diols
  88. Lanthanide(III) and Group IV metal triflate catalysed electrophilic nitration: ‘nitrate capture’ and the rôle of the metal centre †
  89. Ytterbium(III) triflate-catalysed preparation of calix[4]resorcinarenes: Lewis assisted Brønsted acidity
  90. Rapid Entry into Mono-, Bi-, and Tricyclic β-Lactam Arrays via Alkene Metathesis
  91. Nucleophilic Substitution Reactions of (Alkoxymethylene)dimethylammonium Chloride
  92. Diastereoselective Conjugate Addition to (+)-Camphorsulfonic Acid Derived Nitroalkenes:  Synthesis of α-Hydroxy and α-Amino Acids
  93. Scandium(III) or lanthanide(III) triflates as recyclable catalysts for the direct acetylation of alcohols with acetic acid
  94. Lanthanide(iii) triflates as recyclable catalysts for atom economic aromatic nitration
  95. Enantioselective synthesis of homoallylic alcohols using (E)-but-2-enyl-trichlorosilane and chiral diamines
  96. Enyne metathesis for the facile synthesis of highly functionalised novel bicyclic β-lactams
  97. Nucleophilic substitution of (alkoxymethylene)dimethylammonium chloride with potassium phthalimide; a convenient procedure for the synthesis of imides with inversion of configuration
  98. Stereochemistry of the catalysed Diels–Alder reaction between cyclopentadiene and dimethyl monothionofumarate; soft versus hard Lewis acids
  99. Oxidation and Reduction