124647-06-9

Upstream product

• 4520-29-0 1,3-bis(trimethylsiloxy)benzene 
• 96863-21-7 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl dimethylphosphinothioate 
• 125343-69-3 2,3,4,6-tetra-O-benzyl-1-O-(trifluoroacetyl)-α-D-glucopyranose 
• 124647-05-8 1-α-O-(3,5-dinitro-benzoyl)-2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 

Relevant academic research and scientific papers

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

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

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.