125164-10-5Relevant articles and documents
A short access to the macrocyclic core of cycloviracin and glucolipsin
Bailliez, Vincent,Figueiredo, Renata M. de,Olesker, Alain,Cleophax, Jeannine
, p. 9151 - 9154 (2007/10/03)
The macrocyclic core of cycloviracin and glucolipsin has been synthesised in ten steps from levoglucosan and (S)-(-)-dimethyl malate. The limited number of steps to obtain this macrolide makes it a valuable procedure for the synthesis of analogues of cycl
A concise synthesis of the fully functional lactide core of cycloviracin B with implications for the structural assignment of related glycolipids
Fuerstner, Alois,Albert, Martin,Mlynarski, Jacek,Matheu, Maribel
, p. 1168 - 1169 (2007/10/03)
The absolute stereochemistry at the site of attachment of the fatty acid residues to the lactide core of the glycolipids cycloviracin B1 (1) and glucolipsin A (13) has been elucidated as (3R,3-R) by comparison of their 13C NMR data w
Synthesis of a pentasaccharide and a heptasaccharide corresponding to an ovarian glycoprotein; studies towards glycosylations
Spijker,Westerduin,Van Boeckel
, p. 6297 - 6316 (2007/10/02)
The syntheses of pentasaccharide I and heptasaccharide II, which correspond to an ovarian O-glycoprotein, are presented. The protected pentasaccharide 1 was prepared by condensing a trisaccharide donor (18c) with a disaccharide acceptor (8b), while conden