58479-67-7

Upstream product

• 58479-62-2 (2R,3S,4S,5R,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-6-methoxy-tetrahydro-pyran-3,4,5-triol 
• 100-39-0 benzyl bromide 
• 53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 97-30-3 methyl-alpha-D-glucopyranoside 

Downstream Products

• 58479-62-2 (2R,3S,4S,5R,6S)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-6-methoxy-tetrahydro-pyran-3,4,5-triol 
• 53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 503173-63-5 1-O-acetyl-2,3,4-tri-O-benzyl-6-O-tert-butyldiphenylsilyl-α-D-glucopyranoside 
• 441018-00-4 Acetic acid (2R,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-iodo-tetrahydro-pyran-2-ylmethoxy)-tetrahydro-pyran-2-ylmethyl ester 
• 153541-58-3 1-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 145149-86-6 O-(6-O-Acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranosyl)-(1->6)-1-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranose 

Relevant academic research and scientific papers

Solution- and solid-phase oligosaccharide synthesis using glucosyl iodides: a comparative study

Glycosyl iodide donors have been used in both solid- and solution-phase syntheses yielding α-(1->6)-linked glucosyl oligomers in highly efficient protocols. While the solid-phase strategy offers advantages in terms of ease of purification, it requires a t

Synthesis of aminophosphonate haptens for an aminoacylation reaction between methyl glucoside and a β-alanyl ester

Two 2-aminophosphonate haptens derived from methyl α-D-glucopyranoside were synthesized to mimic the transition-state of a transesterification reaction between methyl α-D-glucopyranoside and 4-nitrophenylester of tert-BOC-β-alanine. Two sets of monoclonal

Novel Silylating Agents Employing 4-Pentenyl Silyl Ethers

Nonsymmetrical silaketals R'OSiR2OR" other than R = Me were efficiently prepared by the activation of 4-pentenyl silyl ethers with IDCP in the presence of an alcohol.In addition, trialkylsilyl ethers could be prepared from the corresponding trialkylsilyl

Carbohydrate biguanides as potential hypoglycemic agents

A series of monosaccharides containing a biguanide functionality was prepared and evaluated for hypoglycemic activity. Among the analogues prepared were those involving D-glucose substituted on the 6- or 1- position (19 and 24), D-galactose substituted on