Cyclohexan‐1,2‐diacetale (CDA): eine neue Schutzgruppe für vicinale Diole in Kohlenhydraten
暂无分享,去创建一个
[1] S. V. Ley,et al. Eintopfsynthese einer Trisaccharideinheit des gemeinen Polysaccharid-Antigens von Streptococci der Gruppe B unter Verwendung Cyclohexan-1,2-diacetal(CDA)-geschützter Rhamnoside† , 1994 .
[2] S. Ley,et al. Dispiroketals in synthesis (part 7): Protection of D-glucopyranose substrates☆ , 1994 .
[3] S. Oscarson,et al. Syntheses of the octyl and tetradecyl glycosides of 3,6-di-O-α-d-mannopyranosyl-α-d-mannopyranose and of 3,4-di-O-α-d-mannopyranosyl-α-d-mannopyranose. A new way for 2,4-di-O-protection of mannopyranosides , 1993 .
[4] S. Ley,et al. Dispiroketals in synthesis (Part 5): A new opportunity for oligosaccharide synthesis using differentially activated glycosyl donors and acceptors , 1993 .
[5] S. Ley,et al. Dispiroketals in synthesis (part 2): A new group for the selective protection of diequatorial vicinal diols in carbohydrates. , 1992 .
[6] J. Brisson,et al. Synthetic oligosaccharides related to Group B streptococcal polysaccharides. The rhamnotriose moiety of the common antigen , 1987 .
[7] D. I. Rawson,et al. Assignment of ring size in isopropylidene acetals by 13C N.M.R. , 1980 .
[8] F. W. Parrish,et al. Monomolar acetalations of methyl α-d-mannosides—synthesis of methyl α-d-talopyranoside , 1977 .