Influence of the O3 Protecting Group on Stereoselectivity in the Preparation of C-Mannopyranosides with 4,6-O-Benzylidene Protected Donors

Lignende værker

• Is Donor-Acceptor Hydrogen Bonding Necessary for 4,6-O-Benzylidene-directed β-Mannopyranosylation? Stereoselective Synthesis of β-C-Mannopyranosides and α-C-Glucopyranosides
  af: Crich, David, et al.
  Udgivet: (2008)
• Influence of Protecting Groups on the Anomeric Equilibrium; Case of the 4,6-O-Benzylidene Acetal in the Mannopyranose Series
  af: Sharma, Indrajeet, et al.
  Udgivet: (2012)
• Stereoselective C-Glycoside Formation with 2-O-Benzyl-4,6-O-benzylidene Protected 3-Deoxy Gluco-and Mannopyranoside Donors: Comparison with O-Glycoside Formation
  af: Moumé-Pymbock, Myriame, et al.
  Udgivet: (2012)
• On the regioselectivity of the Hanessian–Hullar reaction in 4,6-O-benzylidene protected galactopyranosides
  af: Crich, David, et al.
  Udgivet: (2006)
• Direct Stereocontrolled Synthesis of 3-Amino-3-deoxy-β-Mannopyranosides: Importance of the Nitrogen Protecting Group on Stereoselectivity
  af: Crich, David, et al.
  Udgivet: (2007)