All Stories

  1. Visible‐Light‐Promoted Dearomatization for The Construction of Imidazole Scaffolds
  2. Eco-Friendly Synthesis of Aminophosphonates with Unique Fluorescence
  3. Metal‐Free Aminophosphonation: Eco‐Friendly Synthesis and Photophysical Properties of Fluorescent 3‐(Aminoimidazo[1,2‐a]Pyridin‐2‐yl)Phosphonates
  4. (Ph3P)AuCl-catalyzed homocoupling of arylboronic acids under benchtop conditions: Synthesis of biphenyls
  5. Synthesis of 3,4-Dihydropyrimidin(thio)one Containing Scaffold: Biginelli-like Reactions
  6. Discovering Efficient Cobalt Catalysts for Selective Chemical Reactions
  7. Synthesis of Ketones by C−H Functionalization of Aldehydes with Boronic Acids under Transition‐Metal‐Free Conditions
  8. Unlocking a Chemistry's Secret: Nitrosobenzene Unleashes Aldehyde Power for C-H to C-C Conversion
  9. How to make C–N bonds using boronic acids without transition metals
  10. Unlocking the Power of “Boronics”: Easy Method for Creating Tertiary Aryl Amines from “Nitros”
  11. Mono-N-Methyl/Alkyl Amines: Synthesis without overalkylation
  12. Making Flufenamic Acid with Boronic Acids & Nitrosoarenes – A Lab Adventure for Chemistry Students
  13. Selective Functionalization of Achmatowicz Rearrangement Products by Reactions with Potassium Organotrifluoroborates under Transition-Metal-Free Conditions
  14. Metal-Free Organocatalysis
  15. Synthesis of Di(hetero)arylamines from Nitrosoarenes and Boronic Acids: A General, Mild, and Transition-Metal-Free Coupling
  16. Towards understanding the behavior of polyelectrolyte–surfactant mixtures at the water/vapor interface closer to technologically-relevant conditions
  17. Transition-Metal-Free Stereocomplementary Cross-Coupling of Diols with Boronic Acids as Nucleophiles
  18. C–C Bond Formation with Boronic Acids and Derivatives by Tran­sition-Metal-Free Conjugate Addition Reactions
  19. Ring-Opening of Donor–Acceptor Cyclopropanes by Boronic Acids and Potassium Organotrifluoroborates under Transition-Metal-Free Conditions
  20. Transition-metal free reactions of boronic acids: cascade addition – ring-opening of furans towards functionalized γ-ketoaldehydes
  21. Metal-Free Conjugate Addition of Alkenylboronic Acids to Enedicarbonyl Compounds towards the Synthesis of Pyridazine Derivatives
  22. Transition-Metal-Free Direct anti-Carboboration of Alkynes with Boronic Acids To Produce Alkenylheteroarenes
  23. 1,2‐Stereochemical Induction in the PdII‐Catalyzed Conjugate Addition of Boronic Acids
  24. Metal-free ring-opening of epoxides with potassium trifluoroborates
  25. Transition-metal-free C–C bond forming reactions of aryl, alkenyl and alkynylboronic acids and their derivatives
  26. Transition-Metal-Free Reactions of Boronic Acids: 1,3-Stereochemical Induction in the Substrate-Controlled Conjugate Addition
  27. Discovery of alkenylboronic acids as neuroprotective agents affecting multiple biological targets involved in Alzheimer’s disease
  28. Stereoselective Synthesis of Indanylglycine Derivatives by a Tandem Michael–Michael Reaction
  29. PdII‐Catalyzed Conjugate Addition of Boronic Acids to Ketoglutaconic Esters toward the Synthesis of Functionalized Pyridazin‐3(2H)‐ones with Neuroprotective Activity
  30. Trifluoroacetic anhydride—catalyzed conjugate addition of boronic acids to α,β-unsaturated ketones
  31. Trifluoroacetic Anhydride Promoted Tandem Conjugate Addition of Boronic Acids/Acetal Ring Opening
  32. Regioselective 1,6-Conjugate Addition of Boronic Acids and Grignard Reagents to Dienylpyridines
  33. Synthesis and evaluation of arylquinones as BACE1 inhibitors, β-amyloid peptide aggregation inhibitors, and destabilizers of preformed β-amyloid fibrils
  34. In vitro antiamyloidogenic properties of 1,4-naphthoquinones
  35. Conjugate addition reactions of carbon nucleophiles to electron-deficient dienes
  36. N-Heterocyclic Carbene-Catalyzed Monoacylation of 1,4-Naphthoquinones with Aldehydes
  37. Arylation of Benzo-Fused 1,4-Quinones by the Addition of Boronic Acids under Dicationic Pd(II)-Catalysis
  38. 1,6-Conjugate Addition of Boronic Acids to 2-Allylidenemalonates
  39. 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
  40. Diastereoselective Synthesis of 1,2,3-Trisubstituted Indanes via Rhodium(I)-Catalyzed Tandem Conjugate Additions
  41. Stereoselective Rhodium-Catalyzed Conjugate Addition of Boronic Acids to Unprotected δ-Hydroxy-γ-butenolides. Synthesis of (−)-7-Oxamuricatacin and β-Substituted Derivatives
  42. Stereoselective RhI-Catalyzed Tandem Conjugate Addition of Boronic Acids−Michael Cyclization
  43. Stereoselective Conjugate Addition of Aryl- and Alkenylboronic Acids to Acyclic γ,δ-Oxygen-Substituted α,β-Enoates
  44. An Efficient Synthesis of Enantiomerically Pure (1R,2S,5S)- and (1S,2R,5R)-Rosaprostol Methyl Esters
  45. Benzylic Substitution of Gramines with Boronic Acids and Rhodium or Iridium Catalysts†
  46. Stereochemistry of the Tetrabutylammonium Cyanide-Catalyzed Cyanosylilation of Cyclic α,β-Epoxyketones – Dependence of the Diastereoselectivity on the Ring Size
  47. Rhodium-Catalyzed Reaction of Aryl- and Alkenylboronic Acids with 2,4-Dienoate Esters:  Conjugate Addition and Heck Reaction Products
  48. Stereoselective Synthesis of Tetrahydrofuran Spiro‐β‐Lactams by Ru‐Catalyzed Metathesis of 7‐Oxabicyclo[2.2.1]heptenes
  49. Stereoselectivity Control in the Rh(I)-Catalyzed Conjugate Additions of Aryl and Alkenylboronic Acids to Unprotected Hydroxycyclopentenones
  50. Tetrabutylammonium cyanide catalyzed diasteroselective cyanosilylation of chiral α-hydroxyketones
  51. The reaction of spiroepoxycyclohexadienones towards cyanide nucleophiles
  52. Asymmetric synthesis of cyclopentenones with benzylic α-quaternary carbon stereogenic centres from furans
  53. 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
  54. Enantioselective Synthesis of γ,δ-Disubstituted β-Hydroxy δ-Lactones from Furans: Synthesis of (+)-Prelactone B and its C-4 Epimer
  55. The Staudinger reaction of imines derived from 7-oxanorbornenone: formation of spiranic oxazinone versus β-lactam rings
  56. Asymmetric C C bond formation by the mixed oxidative coupling of 1,1′-bi-2-naphthyl esters
  57. Diastereoselective Synthesis and Estimation of the Conformational Flexibility of 6-Oxoperhydropyridazine-3-carboxylic Acid Derivatives
  58. Domino Metathesis of 2-Azanorbornenones:  A New Strategy for the Enatioselective Synthesis of 1-Azabicyclic Compounds
  59. On the Reactivity of (7-Oxabicyclo[2.2.1]hept-5-en-2-ylidene)amines. Different Reaction Paths Leading to the Same Final Products
  60. Regio- and Stereoselective Addition of Grignard and Organolithium Reagents to 4-Hydroxy-2-cyclopentenones
  61. Regio- and stereoselective ring-opening dimerization–cross-coupling metathesis of 7-oxanorbornene derivatives
  62. First intermolecular Pauson–Khand reaction of 7-azanorbornenes. Control of the regioselectivity by the effect of the substituents attached to the olefinic partner
  63. Conformationally restricted glutamic acid derivatives: asymmetric synthesis of 4-substituted 4,5-dihydro-3(2H)-pyridazinones
  64. Stereoselective coupling of ketone and carboxylate enolates
  65. Regioselective domino metathesis of 7-oxanorbornene derivatives as a new stereoselective entry into 2,6-dioxabicyclo[4.3.0]nonenes
  66. 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
  67. Synthesis of γ,δ-Didehydrohomoglutamates by the Phosphine-Catalyzed γ-Addition Reaction to Acetylenic Esters
  68. An expeditious entry to the hydrophenalene ring system of pseudopterosins
  69. Regioselective Ring-Opening and Cross-Coupling Metathesis of 2-Substituted 7-Oxanorbornenes. New Stereoselective Entry into Trisubstituted Tetrahydrofurans
  70. Carboxylates as pronucleophiles in the phosphine-catalyzed γ-addition reaction
  71. Control of the Regioselectivity in the Pauson−Khand Reaction of 7-Oxanorbornene Derivatives
  72. Reaction of α,β-unsaturated ketones with LiAlH4 under oxygen: synthesis of 1,3-diols
  73. Study of the asymmetric synthesis of (Z)-γ-substituted α,β-dihehydroglutamates from N-alkylideneglycinates
  74. Diastereoselective synthesis of syn,syn- and syn,anti-2,4-diamino-3-hydroxyglutaric acid derivatives from ethyl α-acyl alaninates
  75. Diastereoselective Aldol Reactions of ( Z )- N -[Bis(methylthio)methylene]-α,β-didehydroglutamates
  76. Reaction of N-[bis(methylthio)methylene]glycinates with electron deficient alkynes. Synthesis of (Z)-α,β-didehydroglutamic acid derivatives
  77. Asymmetric Oxidative Dimerization of the Enolates ofN-[Bis(methylthio)methylene]- andN-(Diphenylmethylene)glycine Esters
  78. On the acylation reactions of aza-allyl carbanions derived from N-[bis(methylthio)methylene]glycine ethyl ester and N-[bis(methylthio)methylene]benzylamine
  79. Diastereoselective reduction of α-acyl-N-[Bis(methylthio)methylene]alaninates and phenylalaninates: Synthesis of α,α-disubstituted β-hydroxy α-amino esters
  80. Diastereoselective Synthesis of α,α-Disubstituted γ-Carboxypyroglutamates via Sm(III)−Azomethine Ylide Cycloadditions
  81. Diastereoselective 1,3-dipolar cycloaddition of Sm(III)-azomethine ylides to α,β-unsaturated esters
  82. Asymmetric Alkylation of 8-Phenylmenthyl N-[Bis(methylthio)methylene]glycinate Enolates. Synthesis of D- and L-.alpha.-Amino Acids from a Single Chiral Precursor
  83. Diastereoselective Synthesis of Substituted Glutamic Acid Derivatives via Michael Additions of N-[Bis(methylthio)methylene]glycinates under Solid-Liquid Phase Transfer Catalysis
  84. Diastereoselective Alkylation of 8-Phenylmenthyl Phenylacetate: Aggregated Lithium Enolate versus "Naked" Enolate
  85. Stereochemistry of Silyl Ketene Acetals of Some 8-Phenylmenthyl Arylacetates
  86. Diastereoselective synthesis of functionalized 2,4-diamino-3-hydroxyglutaric acid derivatives of potential biological interest from glycine derivatives
  87. New aspects in the regioselective functionalization of furans. synthesis of tri-and tetrasubstituted furan derivatives.
  88. Chemoselective reduction in carbonyl-conjugated vinylfurans by the Mg/MeOH system
  89. Synthesis of 2,5-bis-(Ethynyl) furan Derivatives from 2,5-Furandicarboxaldehyde
  90. 1,3-Dipolar cycloadditions of benzonitrile oxide to vinyl and azavinyl furan derivatives
  91. Magnesium monoperoxyphtalate: A new reagent for the oxidative ring opening of furans to cis-enediones
  92. Selective Double Bond Reduction in Carbonyl-Conjugated Vinylfurans