All Stories

  1. Iridium-Catalyzed Reductive Nucleophilic Addition to Secondary Amides
  2. How Do You Increase Total Yield in Natural Product Synthesis?
  3. Synthesis of β-Hydroxy-α,α-disubstituted Amino Acids through the Orthoamide-Type Overman Rearrangement of an α,β-Unsaturated Ester and Stereodivergent Intramolecular SN2′ Reaction: Development and Application to the Total Synthesis of Sphingofungin F
  4. Synthesis of Kaitocephalin Facilitated by Three Stereoselective Allylic Transposition Reactions
  5. Stereodivergent Hydroboration of Allenes
  6. Total synthesis of complex alkaloids by nucleophilic addition to amides
  7. Unified Total Synthesis of Stemoamide-Type Alkaloids by Chemoselective Assembly of Five-Membered Building Blocks
  8. Reductive Approach to Nitrones from N-Siloxyamides and N-Hydroxyamides
  9. Unified Total Synthesis of Madangamines A, C, and E
  10. An Iridium-Catalyzed Reductive Approach to Nitrones from N-Hydroxyamides
  11. Total Synthesis of (–)-Stemoamide by Sequential Overman/Claisen Rearrangement
  12. Practical synthesis of the C-ring precursor of paclitaxel from 3-methoxytoluene
  13. Enantioselective Total Synthesis of (+)-Neostenine
  14. Copper-catalyzed electrophilic amination using N-methoxyamines
  15. Synthesis of (±)-Lasubine II Using N -Methoxyamines
  16. Synthesis of Paclitaxel. 2. Construction of the ABCD Ring and Formal Synthesis
  17. Synthesis of Paclitaxel. 1. Synthesis of the ABC Ring of Paclitaxel by SmI2-Mediated Cyclization
  18. Synthesis of Diazatricyclic Common Structure of Madangamine Alkaloids
  19. Total Syntheses of (±)-Gephyrotoxin and (±)-Perhydrogephyrotoxin
  20. Iridium-Catalyzed Chemoselective Reductive Nucleophilic Addition toN-Methoxyamides
  21. Total Synthesis of Sphingofungin F by Orthoamide-Type Overman Rearrangement of an Unsaturated Ester
  22. Chemoselective Reductive Nucleophilic Addition to Tertiary Amides, Secondary Amides, andN-Methoxyamides
  23. Cover Picture: Two-step Synthesis of Multi-Substituted Amines by Using anN-Methoxy Group as a Reactivity Control Element (Chem. Eur. J. 26/2014)
  24. Two-Step Synthesis of Multi-Substituted Amines by Using anN-Methoxy Group as a Reactivity Control Element
  25. Two-step Synthesis of Multi-Substituted Amines by Using anN-Methoxy Group as a Reactivity Control Element
  26. Nucleophilic addition to N-alkoxyamides
  27. Total Synthesis of (±)-Gephyrotoxin by Amide-Selective Reductive Nucleophilic Addition
  28. Cascade- and Orthoamide-Type Overman Rearrangements of Allylic Vicinal Diols
  29. Synthesis of (−)-Morphine: Application of Sequential Claisen/Claisen Rearrangement of an Allylic Vicinal Diol
  30. Direct Nucleophilic Addition toN-Alkoxyamides
  31. Chirality Transfers through Sequential Sigmatropic Rearrangements of Allylic Vicinal Diols: Development and Application to Total Synthesis of (-)-Kainic Acid
  32. Concise Synthesis of α-Trisubstituted Amines from Ketones UsingN-Methoxyamines
  33. Direct Chemoselective Allylation of Inert Amide Carbonyls
  34. Total Synthesis of Broussonetine F: The Orthoamide Overman Rearrangement of an Allylic Diol
  35. Novel Sequential Sigmatropic Rearrangements of Allylic Diols: Application to the Total Synthesis of (−)-Kainic Acid
  36. Total Synthesis of (−)-Salinosporamide A
  37. A Direct Entry to Substituted N-Methoxyamines from N-Methoxyamides via N-Oxyiminium Ions
  38. Formal Synthesis of Salinosporamide A Starting from d-Glucose
  39. Total Synthesis of (−)-Agelastatin A: The Application of a Sequential Sigmatropic Rearrangement
  40. Construction of Epidithiodioxopiperazines by Directed Oxidation of Hydroxyproline-Derived Dioxopiperazines
  41. Total Synthesis and Bioactivity of an Unnatural Enantiomer of Merrilactone A:  Development of an Enantioselective Desymmetrization Strategy
  42. Asymmetric Total Synthesis of (−)-Merrilactone A: Use of a Bulky Protecting Group as Long-Range Stereocontrolling Element
  43. Total Synthesis of Merrilactone A