501100-98-7

Upstream product

• 105-36-2 ethyl bromoacetate 
• 188819-44-5 1-Deoxy-2,3,4,6-tetra-O-benzyl-β-D-mannopyranosyl cyanide 

Downstream Products

• 501101-21-9 diethyl (4R)-2-(2',3',4',6'-tetra-O-benzyl-β-D-mannopyranosyl)-1,4-dihydro-6-methyl-4-phenylpyridine-3,5-dicarboxylate 
• 501101-20-8 diethyl (4S)-2-(2',3',4',6'-tetra-O-benzyl-β-D-mannopyranosyl)-1,4-dihydro-6-methyl-4-phenylpyridine-3,5-dicarboxylate 
• 885481-11-8 (S)-3-Amino-3-((2S,3R,4R,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-propionic acid ethyl ester 

Relevant academic research and scientific papers

A facile and general entry to C-glycosyl (R)- and (S)-β-amino acid pairs from glycosyl cyanides through enamino ester intermediates

Four O-perbenzylated glycosyl cyanides (α- and β-D- mannopyranosyl, α-D-galactopyranosyl, and α-D-arabinofuranosyl) were converted by treatment with BrCH2CO2Et/Zn in THF at reflux (Blaise-Kishi reaction) into the corresponding C-glyc

Dihydropyridine C-glycoconjugates by Hantzsch cyclocondensation. Synthesis of a C(6)-glycosylated nifedipine analogue

The use of glycosylated reagents in Hantzsch-type cyclocondensation reactions leading to C-glycosylated dihydropyridines (DHPs) has been investigated. A three-component approach with an anomeric sugar aldehyde (galacto, manno, and ribo derivatives), a β-k