82300-66-1Relevant articles and documents
New Synthetic Methods and Reagents for Complex Carbohydrates. IX. Aryl D-Glucopyranosides and 1-Aryl-1-deoxy-D-glucopyranoses from 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl Dimethylphosphinothioate
Yamanoi, takashi,Fujioka, Ayumi,Inazu, Toshiyuki
, p. 1488 - 1491 (2007/10/02)
The reactions of 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl dimethylphosphinothioate and phenolic compounds gave the corresponding aryl α-D-glucopyranosides predominantly in good yields, even when the trimethylsiloxy derivatives of benzene, which are known
STUDIES ON C-GLYCOSIDES. XIII. C-GLUCOSIDES FROM O-GLUCOSYL 3,5-DINITRO BENZOATE
Cai, Meng-Shen,Qiu, Dong-Xu
, p. 851 - 856 (2007/10/02)
From O-glucopyranosyl 3,5-dinitro benzoate (1) and aryl ethers C-glucosides were obtained stereoselectively in the presence of Lewis acid in high yield.In most cases, the β-anomer was formed.
C-GLYCOSIDES FROM O-GLYCOSYL TRICHLOROACETIMIDATES
Schmidt, Richard R.,Hoffmann, Michael
, p. 409 - 412 (2007/10/02)
From O-glycosyl trichloroacetimidates 2, 9, and 13 and activated benzene derivatives C-aryl glycosides were obtained by mild Lewis acid catalysis.In most cases only one stereoisomer was formed, however, the α-alkoxyalkyl transfer took place not always by
