Synthetic approach toward the partial sequences of betaglycan in the linkage region on solid support and in solution phase

…, A Yamaguchi, J Tanaka, Y Nishimura

Index: Tamura, Jun-Ichi; Yamaguchi, Akihiro; Tanaka, Junko; Nishimura, Yuko Journal of Carbohydrate Chemistry, 2007 , vol. 26, # 2 p. 61 - 82

Full Text: HTML

Citation Number: 5

Abstract

We have synthesized, for the first time, the partial sequence of the betaglycan composed of the tetraosyl hexapeptide, which was directly usable as a probe for enzymatic glycosyl transfer. Stepwise elongation afforded the corresponding tetraosyl trichloroacetimidate. The common glycosyl dipeptide:[β??d??GlcA??(1→ 3)?螃漫?d??Gal??(1→ 3)?螃漫?d??Gal??(1→ 4)?螃漫?d??Xyl?? (1→ O)??Ser??Gly] was synthesized by glycosylation of the corresponding tetraosyl ...

Related Articles:

Protic acid immobilized on solid support as an extremely efficient recyclable catalyst system for a direct and atom economical esterification of carboxylic acids with …

[Chakraborti, Asit K.; Singh, Bavneet; Chankeshwara, Sunay V.; Patel, Alpesh R. Journal of Organic Chemistry, 2009 , vol. 74, # 16 p. 5967 - 5974]

More Articles...