All Stories

  1. Flow technology for organometallic-mediated synthesis
  2. Exploiting structural and conformational effects for a site-selective lithiation of azetidines
  3. ChemInform Abstract: Harnessing the ortho-Directing Ability of the Azetidine Ring for the Regioselective and Exhaustive Functionalization of Arenes.
  4. Enantioselective carbolithiation of S-alkenyl-N-aryl thiocarbamates: kinetic and thermodynamic control
  5. Deconstruction of 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline moiety to separate P-glycoprotein (P-gp) activity from σ2 receptor affinity in mixed P-gp/σ2 receptor agents
  6. Easy access to constrained peptidomimetics and 2,2-disubstituted azetidines by the unexpected reactivity profile of α-lithiated N-Boc-azetidines
  7. External Trapping of Halomethyllithium Enabled by Flow Microreactors
  8. Lithium Compounds in Organic Synthesis. From Fundamentals to Applications. Herausgegeben von Renzo Luisi und Vito Capriati.
  9. Lithium Compounds in Organic Synthesis. From Fundamentals to Applications. Edited by Renzo Luisi and Vito Capriati.
  10. Regio- and stereochemistry of Na-mediated reductive cleavage of alkyl aryl ethers
  11. ChemInform Abstract: Complexation Phenomena and Dynamics at Work in the Lithiation Reactions of Small-Ring Heterocycles: Regio- and Stereoselectivity
  12. ChemInform Abstract: Recent Advances in the Stereoselective Synthesis of Aziridines
  13. Recent Advances in the Stereoselective Synthesis of Aziridines
  14. ChemInform Abstract: Expanding the Synthetic Portfolio of Organolithiums: Direct Use in Catalytic Cross-Coupling Reactions
  15. Harnessing theortho-Directing Ability of the Azetidine Ring for the Regioselective and Exhaustive Functionalization of Arenes
  16. Complexation Phenomena and Dynamics at Work in the Lithiation Reactions of Small-Ring Heterocycles: Regio- and Stereoselectivity
  17. Synthesis of Functionalized Arylaziridines as Potential Antimicrobial Agents
  18. ChemInform Abstract: Regioselective Functionalization of 2-Arylazetidines: Evaluating the ortho-Directing Ability of the Azetidinyl Ring and the α-Directing Ability of the N-Substituent.
  19. Expanding the Synthetic Portfolio of Organolithiums: Direct Use in Catalytic Cross-Coupling Reactions
  20. Lithium Compounds in Organic Synthesis
  21. Practical Aspects of Organolithium Chemistry
  22. Nitrogen-Bearing Lithium Compounds in Modern Synthesis
  23. Regioselective functionalization of 2-arylazetidines: evaluating the ortho-directing ability of the azetidinyl ring and the α-directing ability of the N-substituent
  24. Straightforward access to 4-membered sulfurated heterocycles: introducing a strategy for the single and double functionalization of thietane 1-oxide
  25. Stereocontrolled lithiation/trapping of chiral 2-alkylideneaziridines: investigation into the role of the aziridine nitrogen stereodynamics
  26. Correction: Stereocontrolled lithiation/trapping of chiral 2-alkylideneaziridines: investigation into the role of the aziridine nitrogen stereodynamics
  27. ChemInform Abstract: Carbolithiation of S-Alkenyl-N-aryl thiocarbamates: Carbanion Arylation in a Connective Route to Tertiary Thiols.
  28. Commemorating Professor Renzo Galanello (July 21st 1948 - May 13th 2013)
  29. Microreactor-Mediated Organocatalysis: Towards the Development of Sustainable Domino Reactions
  30. Carbolithiation ofS-Alkenyl-N-aryl Thiocarbamates: Carbanion Arylation in a Connective Route to Tertiary Thiols
  31. Synthesis of 1,2,3,4-Tetrahydroisoquinolines by Microreactor-Mediated Thermal Isomerization of Laterally Lithiated Arylaziridines
  32. ChemInform Abstract: One-Pot Preparation of Piperazines by Regioselective Ring-Opening of Non-Activated Arylaziridines.
  33. One-pot preparation of piperazines by regioselective ring-opening of non-activated arylaziridines
  34. Restricted rotations and stereodynamics of aziridine-2-methanol derivatives
  35. Nitrogen Dynamics and Reactivity of Chiral Aziridines: Generation of Configurationally Stable Aziridinyllithium Compounds
  36. BH 3 -Promoted Stereoselective β-Lithiation of N -Alkyl-2-phenylaziridines
  37. ChemInform Abstract: Aziridinyl Anions: Generation, Reactivity, and Use in Modern Synthetic Chemistry
  38. Solvent- and Temperature-Dependent Functionalisation of Enantioenriched Aziridines
  39. Aziridinyl Anions: Generation, Reactivity, and Use in Modern Synthetic Chemistry
  40. ChemInform Abstract: Boron Azaenolates of Chiral Oxazolines: Synthesis of Optically Active Formyl Oxiranes.
  41. ChemInform Abstract: New Arylaziridinyldifluoroborates: Useful Suzuki-Miyaura Reagents.
  42. ChemInform Abstract: Highly Stereoselective Synthesis of Optically Active Oxazolinyl Oxiranes from Azaenolates of a Chiral 2-Chloromethyloxazoline.
  43. ChemInform Abstract: Critical Survey Covering the Year 2007 Organometallic Compounds in Organic Synthesis
  44. ChemInform Abstract: A Stereospecific Synthesis of Oxazolinyloxiranes.
  45. ChemInform Abstract: On the Coupling Reaction of Lithium Azaenolates of Chiral Oxazolines with Carbonyl Compounds.
  46. ChemInform Abstract: A Highly Stereoselective Synthesis of α,β-Unsaturated Oxazolines.
  47. ChemInform Abstract: Lithiation of 2-(1-Chloroethyl)-2-oxazolines: Synthesis of Substituted Oxazolinyloxiranes and Oxazolinylaziridines.
  48. ChemInform Abstract: Stereospecific β-Lithiation of Oxazolinyloxiranes: Synthesis of α,β-Epoxy-γ-butyrolactones
  49. ChemInform Abstract: Oxiranyl Anion Mediated Synthesis of Highly Enantiomerically Enriched Styrene Oxide Derivatives.
  50. New Arylaziridinyldifluoroborates: Useful Suzuki-Miyaura Reagents
  51. Terminal oxazolinyloxiranes: synthesis, reaction with amines and regioselective β-lithiation
  52. Lithiation of N -Alkyl-( o -tolyl)aziridine: Stereoselective Synthesis of Isochromans §
  53. ChemInform Abstract: Synthesis of Optically Active Arylaziridines by Regio- and Stereospecific Lithiation of N-Bus-phenylaziridine.
  54. Synthesis of Optically Active Arylaziridines by Regio- and Stereospecific Lithiation of N -Bus-Phenylaziridine
  55. Influence of an ortho-sulfinyl group on the configurational stability of α-lithiated aryloxiranes: deuteration of tolylsulfinyl styrene oxides
  56. 2-Lithio-3,3-dimethyl-2-oxazolinyloxirane: Carbanion or Azaenolate? Structure, Configurational Stability, and Stereodynamics in Solution
  57. α- vs Ortho-Lithiation of N -Alkylarylaziridines: Probing the Role of the Nitrogen Inversion Process †
  58. Crystal structure of (2R*,3R*)-3-amino-2-ethyl-N-(2-hydroxy-1,1- dimethylethyl)-3-p-methoxyphenylpropanamide, C17H28N2O3
  59. Crystal structure of (+)-(2S,3S,1'S)-2-ethyl-N-(1-hydroxymethyl-2- methylpropyl)-2-methyl-3-phenyl-3-phenylamino propanamide, C23H32N2O2
  60. ChemInform Abstract: Michael Addition of ortho-Lithiated Aryloxiranes to α,β-Unsaturated Malonates: Synthesis of Tetrahydroindenofuranones.
  61. ChemInform Abstract: α-Substituted α-Lithiated Oxiranes: Useful Reactive Intermediates
  62. A computational study of the effect of C-lithiation on the NMR properties (chemical shifts and coupling constants) of aziridines
  63. α-Substituted α-Lithiated Oxiranes: Useful Reactive Intermediates
  64. Michael Addition of Ortho-Lithiated Aryloxiranes to α,β-Unsaturated Malonates: Synthesis of Tetrahydroindenofuranones
  65. Regio- and Stereoselective Lithiation of 2,3-Diphenylaziridines:  A Multinuclear NMR Investigation
  66. ChemInform Abstract: Oxazoline-Mediated Highly Stereoselective Synthesis of α,β-Substituted-β-aminoalkanamides, Potential Precursors of Unnatural β2,2,3-Amino Acids.
  67. Synthesis of 2,3-Dihydro-10bH-oxazolo[2,3-a]isoquinolines from ortho-Lithiated Phenyloxazolinyloxiranes.
  68. Regio- and Stereoselective Lithiation of Terminal Oxazolinylaziridines: The Aziridine N-Substituent and the Oxazolinyl Group Effect.
  69. Oxazoline-mediated highly stereoselective synthesis of α,β-substituted-β-aminoalkanamides, potential precursors of unnatural β2,2,3-amino acids
  70. Asymmetric synthesis of α,β-substituted β-aminoalkanamides and stereochemical determination
  71. Synthesis of 2,3-Dihydro-10b H -oxazolo[2,3- a ]isoquinolines from ortho -Lithiated Phenyloxazolinyloxiranes †
  72. Regio- and Stereoselective Lithiation of Terminal Oxazolinylaziridines:  The Aziridine N -Substituent and the Oxazolinyl Group Effect †
  73. Regio- and Stereoselective Lithiation and Electrophilic Substitution Reactions of N -Alkyl-2,3-diphenylaziridines:  Solvent Effect †
  74. Stereoselective Synthesis of Novel 4,5-Epoxy-1,2-oxazin-6-ones and α,β-Epoxy-γ-amino Acids from β-Lithiated Oxazolinyloxiranes and Nitrones.
  75. Stereoselective Synthesis of Novel β,γ-Epoxyhydroxylamines and 4-Hydroxyalkyl-1,2-oxazetidines.
  76. Stereoselective Synthesis of Novel 4,5-Epoxy-1,2-oxazin-6-ones and α,β-Epoxy-γ-amino Acids from β-Lithiated Oxazolinyloxiranes and Nitrones
  77. Synthesis of 1,3-Dihydrobenzo[c]furans from ortho-Lithiated Aryloxiranes.
  78. Stereoselective Synthesis of Novel 4,5-Epoxy-1,2-oxazin-6-ones and α,β-Epoxy-γ-amino Acids from β-Lithiated Oxazolinyloxiranes and Nitrones
  79. Stereoselective Synthesis of Novel β,γ-Epoxyhydroxylamines and 4-Hydroxyalkyl-1,2-oxazetidines
  80. Synthesis of 1,3-Dihydrobenzo[ c ]furans from Ortho-Lithiated Aryloxiranes
  81. An Efficient Route to Tetrahydronaphthols via Addition of ortho-Lithiated Stilbene Oxides to α,β-Unsaturated Fischer Carbene Complexes.
  82. Directed ortho-Lithiation of N-Alkylphenylaziridines.
  83. Asymmetric Synthesis of Cyclopropanes from Lithiated Aryloxiranes and α,β-Unsaturated Fischer Carbene Complexes.
  84. An Efficient Route to Tetrahydronaphthols via Addition of Ortho-Lithiated Stilbene Oxides to α,β-Unsaturated Fischer Carbene Complexes
  85. α-Lithiated Aryloxiranes: Useful Reactive Intermediates
  86. Asymmetric Synthesis of Cyclopropanes from Lithiated Aryloxiranes and α,β-Unsaturated Fischer Carbene Complexes.
  87. Directed Ortho Lithiation of N -Alkylphenylaziridines
  88. α-Chloroalkylheterocycles: Utility in Synthetic Organic Chemistry
  89. Asymmetric Synthesis of Cyclopropanes from Lithiated Aryloxiranes and α,β-Unsaturated Fischer Carbene Complexes
  90. Stereoselective Synthesis of Pentacarbonyl(3-oxa-2-bicyclo[3.1.0]hexylidene)- and Pentacarbonyl(cyclopropylmethoxymethylene)tungsten Compounds on the Route to Cyclopropane-?-lactones and -carboxylates.
  91. Synthesis and lithiation of oxazolinylaziridines: the N-substituent effect
  92. Synthesis of α-Oxazolinylalkanamides.
  93. α-Lithiated Aryloxiranes: Useful Reactive Intermediates
  94. Stereoselective Synthesis of Pentacarbonyl(3-oxa-2-bicyclo[3.1.0]hexylidene)- and Pentacarbonyl(cyclopropylmethoxymethylene)tungsten Compounds on the Route to Cyclopropane-γ-lactones and -carboxylates
  95. Synthetic Approach to Substituted Cyclopropanes Based on the Coupling Reaction of Lithiated Chloroalkyloxazolines with Fischer Carbene Complexes.
  96. Lithiated α-Chloroalkylheterocycles: Utility in Synthetic Organic Chemistry
  97. Synthesis of α-oxazolinylalkanamides
  98. Stereospecific Synthesis of Optically Active Phenylpropylene Oxides.
  99. Vicarious Nucleophilic Substitution of (Chloroalkyl)heterocycles with Nitroarenes.
  100. Synthetic Approach To Substituted Cyclopropanes Based on the Coupling Reaction of Lithiated Chloroalkyloxazolines with Fischer Carbene Complexes
  101. One-Pot Regioselective Synthesis of Nitrophenyloxazolinyl Styrene Oxides by the Darzens Reaction of Vicarious Nucleophilic Substitution-Formed Carbanions of 2-Dichloromethyl-4,4-dimethyloxazoline
  102. Stereoselective Synthesis of Heterosubstituted Aziridines and Their Functionalization.
  103. Synthesis of Enantiomerically Enriched Oxazolinyl[1,2]oxazetidines.
  104. Stereospecific Synthesis of Optically Active Phenylpropylene Oxides
  105. Vicarious Nucleophilic Substitution of (Chloroalkyl)heterocycles with Nitroarenes
  106. New Synthesis of Optically Active 5-Isoxazolidinones and β-Amino Acids.
  107. Oxazolinyloxiranyllithium-Mediated Synthesis of Highly Strained Heterocyclic Compounds.
  108. Stereoselective synthesis of heterosubstituted aziridines and their functionalization
  109. Oxazolinyloxiranyllithium-mediated synthesis of highly strained heterocyclic compounds
  110. Lithiation of optically active oxazolinyloxiranes: configurational stability
  111. New Synthesis of Optically Active 5-Isoxazolidinones and β-Amino Acids
  112. Synthesis of Enantiomerically Enriched Oxazolinyl[1,2]Oxazetidines
  113. Oxazolinyloxiranyllithium-Mediated Stereoselective Synthesis of α-Epoxy-β-amino Acids.
  114. Isomerization of Oxazolinyl Allylic Alcohols: Synthesis of 3-Alkylidene-2-iminooxetanes.
  115. Oxazolinyloxiranyllithium-Mediated Stereoselective Synthesis of α-Epoxy-β-amino Acids†
  116. Lithiation of Oxazolinylaziridines.
  117. Synthesis of Allylic Alcohols from Oxazolinyloxiranes.
  118. Isomerization of oxazolinyl allylic alcohols: synthesis of 3-alkylidene-2-iminooxetanes
  119. On the lithiation of oxazolinylaziridines
  120. Michael Addition of Chloroalkyloxazolines to Electron-Poor Alkenes:  Synthesis of Heterosubstituted Cyclopropanes†
  121. An Unexpected Base-Promoted Isomerization of Oxazolinylaryl Oxiranes: Synthesis of Oxazolinylaryl Alkanones.
  122. On the Addition of Lithiated 2-Alkyloxazolines to Nitrones: Stereoselective Synthesis of Oxazetidines and Isoxazolidinones
  123. Lithiated Styrene Oxides: Influence of the C-Li Bond Nature on Their Reactivity
  124. Synthesis of Allylic Alcohols from Oxazolinyloxiranes
  125. An unexpected base-promoted isomerization of oxazolinylaryl oxiranes: synthesis of oxazolinylaryl alkanones
  126. On the Addition of Lithiated 2-Alkyl- and 2-(Chloroalkyl)-4,5-dihydro-1,3-oxazoles to Nitrones − A Mechanistic Investigation
  127. Oxiranyl Anion-Mediated Synthesis of Highly Enantiomerically Enriched Styrene Oxide Derivatives
  128. Stereospecific β-Lithiation of Oxazolinyloxiranes:  Synthesis of α,β-Epoxy-γ-butyrolactones
  129. Metalation of 2-Chloromethyl-2-oxazolines:  Synthesis of 1,2,3-Tris(oxazolinyl)cyclopropanes and Derivatives
  130. A highly stereoselective synthesis of α,β-unsaturated oxazolines
  131. On the coupling reaction of lithium azaenolates of chiral oxazolines with carbonyl compounds
  132. Azaenolates of 2-Chloromethyl-4-methoxymethyl-5-phenyl-2-oxazoline − A Highly Diastereo- and Enantioselective Synthesis of Oxazolinyloxiranes
  133. A Stereospecific Synthesis of Oxazolinyloxiranes ⊥
  134. ChemInform Abstract: Oxiranyllithium Based Synthesis of α-Keto-2-oxazolines.
  135. Lithiation of 2-(1-Chloroethyl)-2-oxazolines: Synthesis of Substituted Oxazolinyloxiranes and Oxazolinylaziridines
  136. Oxiranyllithium based synthesis of α-keto-2-oxazolines
  137. Highly stereoselective synthesis of optically active oxazolinyl oxiranes from azaenolates of a chiral 2-chloromethyloxazoline
  138. Boron azaenolates of chiral oxazolines: synthesis of optically active formyl oxiranes
  139. An oxazoline-mediated synthesis of formyl epoxides
  140. Professor Renzo De Felice and the Fascist Phenomenon