130780-27-7

Upstream product

• 106988-66-3 3,4-di-O-benzyl-2,6-dideoxy-D-ribo-hexopyranoside 
• 135-19-3 β-naphthol 
• 130780-25-5 C₂₂H₂₂O₇ 
• 102919-79-9 methyl α-D-digitoxoside 
• 88999-66-0 C₂₂H₂₂O₇ 
• 32469-90-2 methyl 3,4-di-O-benzoyl-2,6-dideoxy-α-D-ribohexopyranoside 
• 64429-65-8 methyl 3,4-di-O-benzoyl-2,6-dideoxy-β-L-lyxo-hexopyranoside 
• 106988-66-3 C₂₀H₂₀O₆ 

Relevant academic research and scientific papers

Aryl and Allyl C-Glycosidation Methods Using Unprotected Sugars

Practical and highly stereoselective aryl and allyl C-glycosidation methods using unprotected sugars as glycosyl donors have been developed. Aryl C-glycosidations of several unprotected 2-deoxy sugars with phenol and naphthol derivatives by the combined u

C-Arylglycosylation of Unprotected Free Sugar

Highly regio- and stereo-selective C-arylglycosylations of the protected free sugars 1-4, the unprotected methyl glycosides 6-9 and the unprotected free sugars 10 and 11 with 2-naphthol 5 are effectively realized by the combined use of TMSOTf-AgClO4 (TMSO

Efficient C-arylglycosylation of 1-O-methyl sugar by novel use of TMSOTf-AgClO4 catalyst system

Highly β-stereoselective C-arylglycosylations of the 1-O-methyl sugars 1-4 with 2-naphthol (9) were effectively achieved by novel combinational use of a catalytic amount of TMSOTf-AgClO4 as an activator. Also, C-arylglycosylations of the 1-O-ac

Improvement in O -> C Glycoside Rearrangement Approach to C-Aryl Glycosides: Use of 1-O-Acetyl Sugar as Stable but Efficient Glycosyl Donor

1-O-Acetyl sugars serve as efficient glycosyl donor in the O -> C-glycoside rearrangement approach to C-aryl glycosides.Model study was carried out on three types of 2-deoxy-glycosyl acetates including amino sugar derivative.Comparison of the promoters, Cp2HfCl2-AgClO4, SnCl4, BF3*OEt2 is described.