All Stories

  1. Conformation–activity relationships of polyketide natural products
  2. Draft Genome Sequence of Gephyronic Acid Producer Cystobacter violaceus Strain Cb vi76
  3. Ether Transfer Methodology: Application to the Synthesis of Polyketide Natural Products
  4. Stereoselective Synthesis of the C9–C19 Fragment of Lyngbyaloside B and C via Ether Transfer
  5. Application of Stereoselective Ether Transfer to the Synthesis of Isotactic Polyethers
  6. ChemInform Abstract: A Formal Total Synthesis of Epothilone A: Enantioselective Preparation of the C1-C6 and C7-C12 Fragments
  7. ChemInform Abstract: Conformational Properties of Epothilone.
  8. ChemInform Abstract: Structural Diversity Based on Cyclopropane Scaffolds.
  9. ChemInform Abstract: Synthetic Efforts Towards the Marine Polyketide Peloruside A
  10. New Sources of Chemical Diversity Inspired by Biosynthesis: Rational Design of a Potent Epothilone Analogue
  11. ChemInform Abstract: Concise Enantioselective Total Synthesis of Neopeltolide Macrolactone Highlighted by Ether Transfer.
  12. ChemInform Abstract: Tedanolide and the Evolution of Polyketide Inhibitors of Eukaryotic Protein Synthesis
  13. Concise Enantioselective Total Synthesis of Neopeltolide Macrolactone Highlighted by Ether Transfer
  14. Synthetic efforts towards the marine polyketide peloruside A
  15. Electrophile-Induced Ether Transfer: Stereoselective Synthesis of 2,6-Disubstituted-3,4-Dihydropyrans
  16. ChemInform Abstract: Electrophile-Induced Ether Transfer: An Expedient Route to 2-Cyano-tetrahydropyrans.
  17. Tedanolide and the evolution of polyketide inhibitors of eukaryotic protein synthesis
  18. ChemInform Abstract: Electrophile-Induced Ether Transfer: Stereoselective Synthesis of 2,4,6-Trisubstituted Tetrahydropyrans.
  19. Electrophile-Induced Ether Transfer: Stereoselective Synthesis of 2,4,6-Trisubstituted Tetrahydropyrans
  20. Electrophile-Induced Ether Transfer: Stereoselective Synthesis of 2,4,6-Trisubstituted Tetrahydropyrans
  21. Electrophile-Induced Ether Transfer: A New Approach to Polyketide Structural Units.
  22. Electrophile-Induced Ether Transfer: An Expedient Route to 2-Cyanotetrahydropyrans
  23. Conformation–activity relationships in polyketide natural products. Towards the biologically active conformation of epothilone
  24. Biosynthetic Inspirations: Cationic Approaches to Cyclopropane Formation
  25. Cyclopropane Structural Units from Homoaldol Adducts.
  26. Biosynthetic inspirations: cationic approaches to cyclopropane formation
  27. Cyclopropane Structural Units from Homoaldol Adducts
  28. Conformation−Activity Relationships in Polyketide Natural Products:  A New Perspective on the Rational Design of Epothilone Analogues
  29. The Conformational Properties of Epothilone.
  30. Structural Diversity Based on Cyclopropane Scaffolds
  31. Conformational Properties of Epothilone
  32. A Formal Total Synthesis of Epothilone A:  Enantioselective Preparation of the C1−C6 and C7−C12 Fragments 1
  33. Towards the synthesis of epothilone A: Enantioselective preparation of the thiazole sidechain and macrocyclic ring closure