All Stories

  1. “Taming” Glycosyl Cations

    Article • Trends in Glycoscience and Glycotechnology, May 2020, Forum: Carbohydrates Coming of Age

    Kaname SASAKI

  2. “Taming” Glycosyl Cations

    Article • Trends in Glycoscience and Glycotechnology, May 2020, Forum: Carbohydrates Coming of Age

    Kaname SASAKI

  3. NMR characterization of α- and β-mannopyranurono-2,6-lactones

    Article • Tetrahedron, September 2018, Elsevier

    Kaname SASAKI

  4. 2,6-Lactones as a New Entry in Stereoselective Glycosylations

    Article • Synlett, February 2017, Thieme Publishing Group

    Kaname SASAKI

  5. β-Stereoselective Mannosylation Using 2,6-Lactones

    Article • Journal of the American Chemical Society, November 2016, American Chemical Society (ACS)

    Kaname SASAKI

  6. Pterin-7-carboxamides as a new class of aldose reductase inhibitors

    Article • Bioorganic & Medicinal Chemistry Letters, October 2016, Elsevier

    Kaname SASAKI

  7. α-Methylphenacyl thioesters as convenient thioacid precursors

    Article • Organic & Biomolecular Chemistry, January 2016, Royal Society of Chemistry

    Kaname SASAKI

  8. ChemInform Abstract: Total Synthesis of Vineomycin B2(I).

    Article • ChemInform, March 2014, Wiley

    Kaname SASAKI

  9. Total Synthesis of Vineomycin B2

    Article • Journal of the American Chemical Society, October 2013, American Chemical Society (ACS)

    Kaname SASAKI, Dr Daisuke Takahashi

  10. Exploration of an imide capture/N,N-acyl shift sequence for asparagine native peptide bond formation

    Article • Bioorganic & Medicinal Chemistry, June 2013, Elsevier

    Oleg Melnyk, Kaname SASAKI

  11. Ionic Liquids as Green Solvents for Glycosylation Reactions

    Article • January 2012, Springer Science + Business Media

    Kaname SASAKI, Dr Daisuke Takahashi

  12. ChemInform Abstract: Facile Amide Bond Formation from Carboxylic Acids and Isocyanates.

    Article • ChemInform, August 2011, Wiley

    Kaname SASAKI

  13. Facile Amide Bond Formation from Carboxylic Acids and Isocyanates

    Article • Organic Letters, May 2011, American Chemical Society (ACS)

    Kaname SASAKI

  14. Chemistry with and Around Thioacids

    Article • Phosphorus Sulfur and Silicon and the Related Elements, May 2011, Taylor & Francis

    Kaname SASAKI

  15. Exploring the potential of the β-thiolactones in bioorganic chemistry

    Article • Organic & Biomolecular Chemistry, January 2011, Royal Society of Chemistry

    Kaname SASAKI

  16. Cyclic Peptide Synthesis with Thioacids

    Article • Organic Letters, July 2010, American Chemical Society (ACS)

    Kaname SASAKI

  17. Effective and chemoselective glycosylations using 2,3-unsaturated sugars

    Article • Organic & Biomolecular Chemistry, January 2010, Royal Society of Chemistry

    Kaname SASAKI, Dr Daisuke Takahashi

  18. Chemoselective glycosylations using 2,3-unsaturated-4-keto glycosyl donors

    Article • Organic & Biomolecular Chemistry, January 2010, Royal Society of Chemistry

    Kaname SASAKI, Dr Daisuke Takahashi

  19. Influence of Protecting Groups on the Reactivity and Selectivity of Glycosylation: Chemistry of the 4,6-O-Benzylidene Protected Mannopyranosyl Donors and Related Species

    Article • January 2010, Springer Science + Business Media

    Kaname SASAKI

  20. Reaction of Thioacids with Isocyanates and Isothiocyanates: A Convenient Amide Ligation Process

    Article • Organic Letters, August 2009, American Chemical Society (ACS)

    Kaname SASAKI

  21. One-Pot Syntheses of Dissymmetric Diamides Based on the Chemistry of Cyclic Monothioanhydrides. Scope and Limitations and Application to the Synthesis of Glycodipeptides

    Article • The Journal of Organic Chemistry, May 2009, American Chemical Society (ACS)

    Kaname SASAKI

  22. Aryl C-Glycosylation Using an Ionic Liquid Containing a Protic Acid.

    Article • ChemInform, October 2007, Wiley

    Kaname SASAKI

  23. Toward the total synthesis of vineomycin B2: application of an efficient glycosylation methodology using 2,3-unsaturated sugars

    Article • Tetrahedron Letters, September 2007, Elsevier

    Kaname SASAKI

  24. Aryl C-glycosylation using an ionic liquid containing a protic acid

    Article • Tetrahedron Letters, June 2007, Elsevier

    Kaname SASAKI

  25. An Efficient Glycosidation Method Using 2,3-Unsaturated Glycosyl Donors.

    Article • ChemInform, April 2007, Wiley

    Kaname SASAKI

  26. An efficient glycosidation method using 2,3-unsaturated glycosyl donors

    Article • Tetrahedron Letters, December 2006, Elsevier

    Kaname SASAKI

  27. Synthesis of hexopyranosyl acetates and 2,3-disubstituted tetrahydropyrans via chemoselective hydrogenation of hex-2-enopyranosyl acetates

    Article • Tetrahedron Letters, November 2006, Elsevier

    Kaname SASAKI

  28. One-step syntheses of alkyl glycosides and alkyl-substituted DNA oligomers by chemoselective glycosidations using DNA bases

    Article • Tetrahedron Letters, February 2006, Elsevier

    Kaname SASAKI

  29. Environmentally benign β-stereoselective glycosidations of glycosyl phosphites using a reusable heterogeneous solid acid, montmorillonite K-10

    Article • Carbohydrate Research, February 2005, Elsevier

    Kaname SASAKI

  30. A Novel Glycosidation of Glycosyl Fluoride Using a Designed Ionic Liquid and Its Effect on the Stereoselectivity.

    Article • ChemInform, January 2005, Wiley

    Kaname SASAKI

  31. A novel glycosidation of glycosyl fluoride using a designed ionic liquid and its effect on the stereoselectivity

    Article • Tetrahedron Letters, September 2004, Elsevier

    Kaname SASAKI

  32. A novel greener glycosidation using an acid–ionic liquid containing a protic acid

    Article • Tetrahedron Letters, July 2003, Elsevier

    Kaname SASAKI