Simplifying oligosaccharide synthesis: efficient synthesis of lactosamine and siaylated lactosamine oligosaccharide donors
…, E Eichler, WW Wakarchuk, M Gilbert…
Index: Mehta, Seema; Gilbert, Michel; Wakarchuk, Warren W.; Whitfield, Dennis M. Organic Letters, 2000 , vol. 2, # 6 p. 751 - 753
Full Text: HTML
Citation Number: 32
Abstract
A practical sequence is described for converting d-glucosamine into peracetylated Gal (β-1, 4) GlcNTroc (β1-S) Ph and Neu5Ac (α-2, 3) Gal (β-1, 4) GlcNTroc (β1-S) Ph building blocks using a synthetic strategy based on chemoenzymatic oligosaccharide synthesis. The known trichloroethoxycarbonyl, N-Troc, protecting group was selected as a suitable protecting group for both enzymatic and chemical reaction conditions. These oligosaccharide ...
Related Articles:
Odorless Preparation of Thioglycosides and Thio??Michael Adducts of Carbohydrate Derivatives
[Mukherjee, Chinmoy; Misra, Anup Kumar Journal of Carbohydrate Chemistry, 2007 , vol. 26, # 4 p. 213 - 221]
[Ghosh, Tamashree; Santra, Abhishek; Misra, Anup Kumar Beilstein Journal of Organic Chemistry, 2013 , vol. 9, p. 974 - 982]