TY - JOUR
T1 - Chemistry of 1,2-anhydro sugars
AU - Li, Gefei
AU - Noguchi, Masato
AU - Serizawa, Kazunari
AU - Shoda, Shin Ichiro
N1 - Publisher Copyright:
© 2018 Swiss Chemical Society. All rights reserved.
PY - 2018
Y1 - 2018
N2 - The 1,2-anhydro sugars are a class of valuable and versatile intermediates in carbohydrate chemistry. In the first part of this article, a review is given on preparation methods of 1,2-anhydro sugars that are suitably protected. Protected 1,2-anhydro sugars have been widely used as glycosyl donors for the synthesis of glycosyl compounds such as oligosaccharides and nucleosides. In the second part, a brief history and the chemistry of unprotected 1,2-anhydro sugars is described. In the past few years, our research group has developed protection-free methods for synthesis of glycosyl compounds through unprotected 1,2-anhydro sugars as reactive intermediates based on the concept of 'direct anomeric activation'. In this article, the one-step preparation of glycosyl compounds such as thioglycoside derivatives and glycosyl azides by using formamidinium-type dehydrating agents is presented. Furthermore, the initial results on the first detection of unprotected 1,2-anhydro sugar intermediates by NMR measurements are shown along with their full structure characterizations.
AB - The 1,2-anhydro sugars are a class of valuable and versatile intermediates in carbohydrate chemistry. In the first part of this article, a review is given on preparation methods of 1,2-anhydro sugars that are suitably protected. Protected 1,2-anhydro sugars have been widely used as glycosyl donors for the synthesis of glycosyl compounds such as oligosaccharides and nucleosides. In the second part, a brief history and the chemistry of unprotected 1,2-anhydro sugars is described. In the past few years, our research group has developed protection-free methods for synthesis of glycosyl compounds through unprotected 1,2-anhydro sugars as reactive intermediates based on the concept of 'direct anomeric activation'. In this article, the one-step preparation of glycosyl compounds such as thioglycoside derivatives and glycosyl azides by using formamidinium-type dehydrating agents is presented. Furthermore, the initial results on the first detection of unprotected 1,2-anhydro sugar intermediates by NMR measurements are shown along with their full structure characterizations.
KW - 1,2-Anhydro sugar
KW - 2-Chloro-1,3-dimethylimidazolinium chloride (DMC)
KW - Direct anomeric activation
KW - Glycosyl Bunte-salt
KW - Glycosyl azide
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U2 - 10.2533/chimia.2018.874
DO - 10.2533/chimia.2018.874
M3 - Article
C2 - 30648954
AN - SCOPUS:85060055341
SN - 0009-4293
VL - 72
SP - 874
EP - 881
JO - Chimia
JF - Chimia
IS - 12
ER -