Syntheses of spacer-armed carbohydrate model compounds
J Kerékgyártó, Z Nagy, Z Szurmai
Index: Kerekgyarto, Janos; Nagy, Zoltan; Szurmai, Zoltan Carbohydrate Research, 1997 , vol. 297, # 2 p. 107 - 115
Full Text: HTML
Citation Number: 2
Abstract
Commercially available chemicals, such as diethylene glycol, 1, 9-nonanediol, 9-decen-1-ol, 1, 2, 6-hexanetriol, and p-nitrophenol were used to prepare spacer-armed carbohydrate derivatives. Glycosides of d-glucose, N-acetyl-d-glucosamine and 3-O-methyl-d-glucose have been synthesized, carrying reactive groups at the end of the spacer-arms. These glycosides are capable of forming neoglycoproteins. When bromo sugars were reacted ...
Related Articles:
[Gill, G. Bryon; Pattenden, Gerald; Roan, Graeme A. Tetrahedron Letters, 1996 , vol. 37, # 52 p. 9369 - 9372]
[Takao; Nigawara; Nishino; Takagi; Maeda; Tadano; Ogawa Tetrahedron, 1994 , vol. 50, # 19 p. 5681 - 5704]
[Guindon, Yvan; Yoakim, Christiane; Morton, Howard E. Journal of Organic Chemistry, 1984 , vol. 49, # 21 p. 3912 - 3920]
[Alvarez, Eleuterio; Diaz, Maria T.; Perez, Ricardo; Ravelo, Jose L.; Regueiro, Alicia; et al. Journal of Organic Chemistry, 1994 , vol. 59, # 10 p. 2848 - 2876]
[Alvarez, Eleuterio; Diaz, Maria T.; Perez, Ricardo; Ravelo, Jose L.; Regueiro, Alicia; et al. Journal of Organic Chemistry, 1994 , vol. 59, # 10 p. 2848 - 2876]