All Stories

  1. Eco-Friendly Synthesis of Aminophosphonates with Unique Fluorescence
  2. Synthesis of 3,4-Dihydropyrimidin(thio)one Containing Scaffold: Biginelli-like Reactions
  3. Synthesis of Ketones by C−H Functionalization of Aldehydes with Boronic Acids under Transition‐Metal‐Free Conditions
  4. Unlocking a Chemistry's Secret: Nitrosobenzene Unleashes Aldehyde Power for C-H to C-C Conversion
  5. How to make C–N bonds using boronic acids without transition metals
  6. Unlocking the Power of “Boronics”: Easy Method for Creating Tertiary Aryl Amines from “Ar-Nitros”
  7. Mono-N-Methyl/Alkyl Amines: Synthesis without overalkylation
  8. Making Flufenamic Acid with Boronic Acids & Nitrosoarenes – A Lab Adventure for Chemistry Students
  9. Selective Functionalization of Achmatowicz Rearrangement Products by Reactions with Potassium Organotrifluoroborates under Transition-Metal-Free Conditions
  10. Metal-Free Organocatalysis
  11. Synthesis of Di(hetero)arylamines from Nitrosoarenes and Boronic Acids: A General, Mild, and Transition-Metal-Free Coupling
  12. Towards understanding the behavior of polyelectrolyte–surfactant mixtures at the water/vapor interface closer to technologically-relevant conditions
  13. Transition-Metal-Free Stereocomplementary Cross-Coupling of Diols with Boronic Acids as Nucleophiles
  14. C–C Bond Formation with Boronic Acids and Derivatives by Tran­sition-Metal-Free Conjugate Addition Reactions
  15. Ring-Opening of Donor–Acceptor Cyclopropanes by Boronic Acids and Potassium Organotrifluoroborates under Transition-Metal-Free Conditions
  16. Transition-metal free reactions of boronic acids: cascade addition – ring-opening of furans towards functionalized γ-ketoaldehydes
  17. Metal-Free Conjugate Addition of Alkenylboronic Acids to Enedicarbonyl Compounds towards the Synthesis of Pyridazine Derivatives
  18. Transition-Metal-Free Direct anti-Carboboration of Alkynes with Boronic Acids To Produce Alkenylheteroarenes
  19. 1,2‐Stereochemical Induction in the PdII‐Catalyzed Conjugate Addition of Boronic Acids
  20. Metal-free ring-opening of epoxides with potassium trifluoroborates
  21. Transition-metal-free C–C bond forming reactions of aryl, alkenyl and alkynylboronic acids and their derivatives
  22. Transition-Metal-Free Reactions of Boronic Acids: 1,3-Stereochemical Induction in the Substrate-Controlled Conjugate Addition
  23. Discovery of alkenylboronic acids as neuroprotective agents affecting multiple biological targets involved in Alzheimer’s disease
  24. Stereoselective Synthesis of Indanylglycine Derivatives by a Tandem Michael–Michael Reaction
  25. PdII‐Catalyzed Conjugate Addition of Boronic Acids to Ketoglutaconic Esters toward the Synthesis of Functionalized Pyridazin‐3(2H)‐ones with Neuroprotective Activity
  26. Trifluoroacetic anhydride—catalyzed conjugate addition of boronic acids to α,β-unsaturated ketones
  27. Trifluoroacetic Anhydride Promoted Tandem Conjugate Addition of Boronic Acids/Acetal Ring Opening
  28. Regioselective 1,6-Conjugate Addition of Boronic Acids and Grignard Reagents to Dienylpyridines
  29. Synthesis and evaluation of arylquinones as BACE1 inhibitors, β-amyloid peptide aggregation inhibitors, and destabilizers of preformed β-amyloid fibrils
  30. In vitro antiamyloidogenic properties of 1,4-naphthoquinones
  31. Conjugate addition reactions of carbon nucleophiles to electron-deficient dienes
  32. N-Heterocyclic Carbene-Catalyzed Monoacylation of 1,4-Naphthoquinones with Aldehydes
  33. Arylation of Benzo-Fused 1,4-Quinones by the Addition of Boronic Acids under Dicationic Pd(II)-Catalysis
  34. 1,6-Conjugate Addition of Boronic Acids to 2-Allylidenemalonates
  35. A Convenient Approach to Polycyclic Derivatives with a cis‐Fused 2,6‐Dioxabicyclo[4.3.0]nonane System by the Sequence Ring‐Opening/Intramolecular Ring‐Closing Enyne Metathesis/Diels–Alder Reaction
  36. Diastereoselective Synthesis of 1,2,3-Trisubstituted Indanes via Rhodium(I)-Catalyzed Tandem Conjugate Additions
  37. Stereoselective Rhodium-Catalyzed Conjugate Addition of Boronic Acids to Unprotected δ-Hydroxy-γ-butenolides. Synthesis of (−)-7-Oxamuricatacin and β-Substituted Derivatives
  38. Stereoselective RhI-Catalyzed Tandem Conjugate Addition of Boronic Acids−Michael Cyclization
  39. Stereoselective Conjugate Addition of Aryl- and Alkenylboronic Acids to Acyclic γ,δ-Oxygen-Substituted α,β-Enoates
  40. An Efficient Synthesis of Enantiomerically Pure (1R,2S,5S)- and (1S,2R,5R)-Rosaprostol Methyl Esters
  41. Benzylic Substitution of Gramines with Boronic Acids and Rhodium or Iridium Catalysts†
  42. Stereochemistry of the Tetrabutylammonium Cyanide-Catalyzed Cyanosylilation of Cyclic α,β-Epoxyketones – Dependence of the Diastereoselectivity on the Ring Size
  43. Rhodium-Catalyzed Reaction of Aryl- and Alkenylboronic Acids with 2,4-Dienoate Esters:  Conjugate Addition and Heck Reaction Products
  44. Stereoselective Synthesis of Tetrahydrofuran Spiro‐β‐Lactams by Ru‐Catalyzed Metathesis of 7‐Oxabicyclo[2.2.1]heptenes
  45. Stereoselectivity Control in the Rh(I)-Catalyzed Conjugate Additions of Aryl and Alkenylboronic Acids to Unprotected Hydroxycyclopentenones
  46. The reaction of spiroepoxycyclohexadienones towards cyanide nucleophiles
  47. Asymmetric synthesis of cyclopentenones with benzylic α-quaternary carbon stereogenic centres from furans
  48. Control of product distribution in the domino metathesis reactions of N-alkynyl 2-azabicyclo[2.2.1]hept-5-en-3-ones. A convenient synthesis of functionalized γ-lactams and indolizidinones
  49. Enantioselective Synthesis of γ,δ-Disubstituted β-Hydroxy δ-Lactones from Furans: Synthesis of (+)-Prelactone B and its C-4 Epimer
  50. The Staudinger reaction of imines derived from 7-oxanorbornenone: formation of spiranic oxazinone versus β-lactam rings
  51. Asymmetric C C bond formation by the mixed oxidative coupling of 1,1′-bi-2-naphthyl esters
  52. Diastereoselective Synthesis and Estimation of the Conformational Flexibility of 6-Oxoperhydropyridazine-3-carboxylic Acid Derivatives
  53. Domino Metathesis of 2-Azanorbornenones:  A New Strategy for the Enatioselective Synthesis of 1-Azabicyclic Compounds
  54. On the Reactivity of (7-Oxabicyclo[2.2.1]hept-5-en-2-ylidene)amines. Different Reaction Paths Leading to the Same Final Products
  55. Regio- and Stereoselective Addition of Grignard and Organolithium Reagents to 4-Hydroxy-2-cyclopentenones
  56. Regio- and stereoselective ring-opening dimerization–cross-coupling metathesis of 7-oxanorbornene derivatives
  57. First intermolecular Pauson–Khand reaction of 7-azanorbornenes. Control of the regioselectivity by the effect of the substituents attached to the olefinic partner
  58. Conformationally restricted glutamic acid derivatives: asymmetric synthesis of 4-substituted 4,5-dihydro-3(2H)-pyridazinones
  59. Stereoselective coupling of ketone and carboxylate enolates
  60. Regioselective domino metathesis of 7-oxanorbornene derivatives as a new stereoselective entry into 2,6-dioxabicyclo[4.3.0]nonenes
  61. Synthesis of 1,1′-methylenedi[(1 R ,1′ R ,3 R ,3′ R ,5 R ,5′ R )-8-oxabicyclo[3.2.1]oct-6-en-3-ol] and derivatives: precursors of long-chain polyketides
  62. Synthesis of γ,δ-Didehydrohomoglutamates by the Phosphine-Catalyzed γ-Addition Reaction to Acetylenic Esters
  63. An expeditious entry to the hydrophenalene ring system of pseudopterosins
  64. Carboxylates as pronucleophiles in the phosphine-catalyzed γ-addition reaction
  65. Control of the Regioselectivity in the Pauson−Khand Reaction of 7-Oxanorbornene Derivatives
  66. Reaction of α,β-unsaturated ketones with LiAlH4 under oxygen: synthesis of 1,3-diols
  67. Study of the asymmetric synthesis of (Z)-γ-substituted α,β-dihehydroglutamates from N-alkylideneglycinates
  68. Diastereoselective synthesis of syn,syn- and syn,anti-2,4-diamino-3-hydroxyglutaric acid derivatives from ethyl α-acyl alaninates
  69. Diastereoselective Aldol Reactions of ( Z )- N -[Bis(methylthio)methylene]-α,β-didehydroglutamates
  70. Reaction of N-[bis(methylthio)methylene]glycinates with electron deficient alkynes. Synthesis of (Z)-α,β-didehydroglutamic acid derivatives
  71. Asymmetric Oxidative Dimerization of the Enolates ofN-[Bis(methylthio)methylene]- andN-(Diphenylmethylene)glycine Esters
  72. On the acylation reactions of aza-allyl carbanions derived from N-[bis(methylthio)methylene]glycine ethyl ester and N-[bis(methylthio)methylene]benzylamine
  73. Diastereoselective Synthesis of α,α-Disubstituted γ-Carboxypyroglutamates via Sm(III)−Azomethine Ylide Cycloadditions
  74. Diastereoselective 1,3-dipolar cycloaddition of Sm(III)-azomethine ylides to α,β-unsaturated esters
  75. Asymmetric Alkylation of 8-Phenylmenthyl N-[Bis(methylthio)methylene]glycinate Enolates. Synthesis of D- and L-.alpha.-Amino Acids from a Single Chiral Precursor
  76. Diastereoselective Synthesis of Substituted Glutamic Acid Derivatives via Michael Additions of N-[Bis(methylthio)methylene]glycinates under Solid-Liquid Phase Transfer Catalysis
  77. Diastereoselective Alkylation of 8-Phenylmenthyl Phenylacetate: Aggregated Lithium Enolate versus "Naked" Enolate
  78. Stereochemistry of Silyl Ketene Acetals of Some 8-Phenylmenthyl Arylacetates
  79. Diastereoselective synthesis of functionalized 2,4-diamino-3-hydroxyglutaric acid derivatives of potential biological interest from glycine derivatives
  80. New aspects in the regioselective functionalization of furans. synthesis of tri-and tetrasubstituted furan derivatives.
  81. Chemoselective reduction in carbonyl-conjugated vinylfurans by the Mg/MeOH system
  82. Synthesis of 2,5-bis-(Ethynyl) furan Derivatives from 2,5-Furandicarboxaldehyde
  83. 1,3-Dipolar cycloadditions of benzonitrile oxide to vinyl and azavinyl furan derivatives
  84. Magnesium monoperoxyphtalate: A new reagent for the oxidative ring opening of furans to cis-enediones
  85. Selective Double Bond Reduction in Carbonyl-Conjugated Vinylfurans