All Stories

  1. Synthetic Applications of Aziridinium Ions
  2. Alkylative Aziridine Ring-Opening Reactions
  3. Preface to “Aziridine Chemistry”
  4. Building Diverse Medicinal Compounds from Aziridines
  5. Editorial: Strained Aza-Heterocycles in Synthesis
  6. Researchers in Korea
  7. Synthesis of 4- to 7-membered Heterocycles by Ring Expansion
  8. ChemInform Abstract: New Perspective on the Synthesis of Aziridine
  9. Atom economical synthesis of oxindoles by metal-catalyzed intramolecular C–C bond formation under solvent-free and aerobic conditions
  10. Stereoselective Pd-catalyzed etherification and asymmetric synthesis of furanomycin and its analogues from a chiral aziridine
  11. Ratiometric fluorescence probes based on a Michael acceptor type of coumarin and their application for the multichannel imaging of in vivo glutathione
  12. Caged rhodamine-based fluorescent probe for biothiol: Selective detection of cysteine over homocysteine and glutathione in water
  13. ChemInform Abstract: Highly Stereoselective Directed Reactions and an Efficient Synthesis of Azafuranoses from a Chiral Aziridine.
  14. ChemInform Abstract: CAL‐B Catalyzed Desymmetrization of 3‐Alkylglutarate: “Olefin Effect” and Asymmetric Synthesis of Pregabalin.
  15. CAL-B catalyzed desymmetrization of 3-alkylglutarate: “olefin effect” and asymmetric synthesis of pregabalin
  16. ChemInform Abstract: Synthesis of 2,5‐Disubstituted 6‐Azaindoles from Substituted Aziridines via Intramolecular Cyclization.
  17. Synthesis of 2,5-Disubstituted 6-Azaindoles from Substituted Aziridines via Intramolecular Cyclization
  18. ChemInform Abstract: Chiral Aziridine‐2‐carboxylates: Versatile Precursors for Functionalized Tetrahydroisoquinoline (THIQ) Containing Heterocycles.
  19. ChemInform Abstract: Regioselectivity in the Ring Opening of Non‐Activated Aziridines
  20. Regioselectivity in the ring opening of non-activated aziridines
  21. Chiral aziridine-2-carboxylates: versatile precursors for functionalized tetrahydroisoquinoline (THIQ) containing heterocycles
  22. Alkylative Ring Opening of N-Methylaziridinium Ions and a Formal Synthesis of Tyroscherin
  23. N-Methylative aziridine ring opening and asymmetric synthesis of MeBmt
  24. 3,4-Disubstituted oxazolidin-2-ones as constrained ceramide analogs with anticancer activities
  25. Fluorescence turn-on probe for biothiols: intramolecular hydrogen bonding effect on the Michael reaction
  26. ChemInform Abstract: Synthesis of 1,2,5‐ and 1,2,3,5‐Substituted Pyrroles from Substituted Aziridines via Ag(I)‐Catalyzed Intramolecular Cyclization.
  27. Synthesis of 1,2,5- and 1,2,3,5-substituted pyrroles from substituted aziridines via Ag(I)-catalyzed intramolecular cyclization
  28. ChemInform Abstract: An Efficient Synthesis of Enantiomerically Pure Aromatic‐Fused N‐Containing Heterocycles from Common Chiral Aziridines.
  29. Asymmetric synthesis of 1-deoxyazasugars from chiral aziridines
  30. An efficient synthesis of enantiomerically pure aromatic-fused N-containing heterocycles from common chiral aziridines
  31. Radiosynthesis and in vitro evaluation of 1‐(tetrahydro‐5‐hydroxy‐6‐(hydroxymethyl)‐2H‐pyran‐3‐yl)‐5‐[125I]iodouracil: A new potential agent for HSV1‐tk reporter gene monitoring
  32. ChemInform Abstract: Conjugate Addition of Amines to Chiral 3‐Aziridin‐2‐yl‐acrylates.
  33. A formal synthesis of (−)-swainsonine from a chiral aziridine
  34. ChemInform Abstract: Selective Reduction of C—C Double Bonds of 2‐Vinylaziridines: Preparation of Enantiomerically Pure 2‐Alkylaziridines.
  35. Conjugate addition of amines to chiral 3-aziridin-2-yl-acrylates
  36. Molecular Basis for the Stereoselective Ammoniolysis of N‐Alkyl Aziridine‐2‐Carboxylates Catalyzed by Candida antarctica Lipase B
  37. ChemInform Abstract: Synthesis of D‐erythro‐Sphingosine from D‐ribo‐Phytosphingosine.
  38. A simple Cu-64 production and its application of Cu-64 ATSM
  39. ChemInform Abstract: The Preparation of Stable Aziridinium Ions and Their Ring Openings.
  40. Nucleophilic substitution of (sulfonyloxymethyl)aziridines: an asymmetric synthesis of both isomers of mexiletine
  41. ChemInform Abstract: Asymmetric Formal Synthesis of (‐)‐Formoterol and (‐)‐Tamsulosin.
  42. The preparation of stable aziridinium ions and their ring-openings
  43. Selective Mono‐BOC Protection of Diamines.
  44. Dihydroxylation of 2‐Vinylaziridine: Efficient Synthesis of D‐ribo‐Phytosphingosine.
  45. Preparation of Enantiopure 2‐Acylazetidine and Their Reactions with Chloroformates.
  46. Selective Mono‐BOC Protection of Diamines
  47. Preparation of enantiopure 2-acylazetidines and their reactions with chloroformates
  48. Asymmetric Formal Synthesis of (-)-Formoterol and (-)-Tamsulosin
  49. Dihydroxylation of 2-vinylaziridine: efficient synthesis ofd-ribo-phytosphingosine
  50. Ring Opening of 2‐Acylaziridines by Acid Chlorides.
  51. Ring opening of 2-acylaziridines by acid chlorides
  52. Synthesis of Constrained Ceramide Analogues and Their Potent Antileukemic Activities.
  53. Synthesis of Functionalized Bicyclic Triazoles from Chiral Aziridines.
  54. Addition Reactions to Chiral Aziridine‐2‐carboxaldimine Toward Various Enantiopure Nitrogen‐Containing Heterocycles.
  55. Lewis Acid‐Catalyzed Stereospecific Ring Expansion of Aziridine‐2‐carboxylates to Imidazolidin‐2‐ones.
  56. Preparation of 2,3‐Diaminopropionate from Ring Opening of Aziridine‐2‐carboxylate.
  57. Addition reactions to chiral aziridine-2-carboxaldimine toward various enantiopure nitrogen-containing heterocycles
  58. Stereoselective Addition of Nucleophiles to Aziridinyl‐2‐carboxaldimine.
  59. Synthesis of Functionalized Bicyclic Triazoles from Chiral Aziridines
  60. Lewis acid-catalyzed stereospecific ring expansion of aziridine-2-carboxylates to imidazolidin-2-ones
  61. Synthesis and antibacterial activity of arylpiperazinyl oxazolidinones with diversification of the N-substituents
  62. Highlights of the Chemistry of Enantiomerically Pure Aziridine‐2‐carboxylates
  63. Novel Synthesis of 4′C‐Aryl‐Branched Acyclic Nucleoside Using [3,3]‐Sigmatropic Rearrangement.
  64. Novel Stereoselective Synthesis of Functionalized Oxazolidinones from Chiral Aziridines.
  65. Stereoselective Reduction of 2-Acylaziridines: An Efficient Synthesis of D-erythro- Sphinganine and Safingol From a Common Intermediate
  66. Synthetic Applications of Lewis Acid Induced N‐Methyleneamine Equivalents
  67. ChemInform Abstract: Synthesis of Substituted‐(l)‐Tryptophanols from an Enantiomerically Pure Aziridine‐2‐methanol.
  68. Synthetic Applications of Lewis Acid-induced N-Methyleneamine Equivalents
  69. FACILE SYNTHESIS OF β-ANILINOPROPIONATES FROM LEWIS ACID-INDUCEDN-METHYLENEANILINES WITH KETENE ACETALS*
  70. An Efficient Synthesis of N-Boc-D-diphenylalanine from a Chiral Azirdine-2-carboxylate
  71. Lipase-catalyzed enantioselective hydrolysis of β-acetyloxymethyl-β-valerolactone
  72. Serotonin Receptor and Transporter Ligands - Current Status
  73. ChemInform Abstract: Stereoselective Synthesis of Protected threo‐β‐Hydroxy‐L‐glutamic Acid Using a Chiral Aziridine.
  74. ChemInform Abstract: Stereocontrolled Iodolactonization of Acyclic Olefinic Amides.
  75. Stereocontrolled Iodolactonization of Acyclic Olefinic Amides
  76. Stereoselective synthesis of protected threo-β-hydroxy-l-glutamic acid using a chiral aziridine
  77. ChemInform Abstract: Formal Synthesis of (‐)‐Serricornin.
  78. Formal Synthesis of (-)-Serricornin
  79. Asymmetric synthesis of 3-amino-2-hydroxy-4-phenylbutanoate
  80. Practical synthesis of Taxol side chain
  81. Synthesis of analogues of 5-aminolaevulinic acid and inhibition of 5-aminolaevulinic acid dehydratase 1
  82. Facile Method for the Monomethylation of Anilines1
  83. Silica gel supported bis-cinchona alkaloid: a highly efficient chiral ligand for heterogeneous asymmetric dihydroxylation of olefins
  84. Addition of 2-Trimethylsilyloxyfuran to Catalytically Generated N-Methyleneamine Equivalents: Synthesis of 5-Aminomethyl-2,5-dihydrofuran-2-ones
  85. Addition of Propargyltrimethylsilane to N-Methyleneamine Equivalents: Generation and Electrophilic Cyclization of Vinylic Carbocations
  86. Efficient and practical polymeric catalysts for heterogeneous asymmetric dihydroxylation of olefins
  87. TiCl4Induced N-Methyleneamine Equivalents. 21. First Synthesis of Anilinomethylazides
  88. Selective Bromination of Ketones. A Convenient Synthesis of 5-Aminolevulinic Acid
  89. Polymeric cinchona alkaloids as catalysts in the enantioselective 2,2-cycloaddition reaction of ketene and chloral
  90. Fungicidal activity of a series of chloroacetylanilidophosphonates
  91. An Efficient Synthesis of Anilinobenzylphosphonates
  92. Stereochemistry in nucleophilic vinylic substitution of activated nitro olefins. 2
  93. TiCl4induced N-Methyleneamine Equivalents: A New Route to Aminoacetonitriles
  94. The synthesis of (3R)-nerolidol
  95. Stereochemistry in nucleophilic vinylic substitution of activated nitro olefins.
  96. Purification and inhibition of spinach .alpha.,.beta.-dihydroxyacid dehydratase
  97. Trichodiene biosynthesis and the role of nerolidyl pyrophosphate in the enzymic cyclization of farnesyl pyrophosphate
  98. Trichodiene biosynthesis and the enzymatic cyclization of nerolidyl pyrophosphate
  99. Trichodiene biosynthesis and the stereochemistry of the enzymatic cyclization of farnesyl pyrophosphate