129575-89-9Relevant articles and documents
Synthesis of glycosyl acceptors by regioselective benzylations of a 2-deoxy-2-phthalimido-D-glucoside
Robina, Inmaculada,Lopez-Barba, Eugenia,Fuentes, Jose
, p. 2847 - 2856 (1996)
The direct regioselective benzylation of p-methoxyphenyl 2-deoxy-2-phthalimido-β-D-glucopyranoside (1) with benzyl bromide under basic conditions gives 4,6-di-O-benzyl (2a), 4-O-benzyl (3a) and 6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 4a. When
Chemoenzymatic approach for the preparation of asymmetric bi-, tri-, and tetra-antennary N-glycans from a common precursor
Gagarinov, Ivan A.,Li, Tiehai,Tora?o, Javier Sastre,Caval, Tomislav,Srivastava, Apoorva D.,Kruijtzer, John A. W.,Heck, Albert J. R.,Boons, Geert-Jan
, p. 1011 - 1018 (2017/05/16)
Progress in glycoscience is hampered by a lack of well-defined complex oligosaccharide standards that are needed to fabricate the next generation of microarrays, to develop analytical protocols to determine exact structures of isolated glycans, and to elu
Use of methanesulfonic acid in the reductive ring-opening of O-benzylidene acetals
Zinin, Alexander I.,Malysheva, Nelly N.,Shpirt, Anna M.,Torgov, Vladimir I.,Kononov, Leonid O.
, p. 627 - 630 (2008/03/13)
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