Nelly N Malysheva

Publications (3)8.52 Total impact

• Article: Stereoselectivity of Glycosylation May Change During the Reaction Course: Highly α‐Stereoselective Sialylation Achieved by Supramer Approach

  Leonid O. Kononov, Nelly N. Malysheva, Anna V. Orlova
  Annalen der Chemie und Pharmacie 12/2008; 2009(5):611 - 616. · 3.10 Impact Factor
• Article: Intermolecular Hydrogen‐Bonding Pattern of a Glycosyl Donor: The Key to Understanding the Outcome of Sialylation

  Leonid O. Kononov, Nelly N. Malysheva, Elena G. Kononova, Anna V. Orlova
  Annalen der Chemie und Pharmacie 05/2008; 2008(19):3251 - 3255. · 3.10 Impact Factor
• Article: Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals.

  Alexander I Zinin, Nelly N Malysheva, Anna M Shpirt, Vladimir I Torgov, Leonid O Kononov
  [show abstract] [hide abstract]
  ABSTRACT: Methanesulfonic acid was shown to be an efficient and convenient substitute for ethereal HCl in reductive 4,6-O-benzylidene acetal ring-opening reaction with sodium cyanoborohydride in THF. Normal regioselectivity was observed, the 6-O-benzyl ethers with free 4-OH group being the major products of the reaction.
  Carbohydrate Research 03/2007; 342(3-4):627-30. · 2.33 Impact Factor