421553-98-2

Upstream product

• 105-36-2 ethyl bromoacetate 
• 359017-25-7 ethyl 3-((2R,3R,4S,5S,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)tetrahydro-2H-pyran-2-yl)-3-oxopropanoate 

Downstream Products

• 501101-15-1 diethyl (4S)-2-(2',3',4',6'-tetra-O-benzyl-β-D-galactopyranosyl)-1,4-dihydro-6-methyl-4-phenylpyridine-3,5-dicarboxylate 
• 421554-05-4 2-Methyl-4-phenyl-6-((2S,3S,4R,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester 

Relevant academic research and scientific papers

Two- and three-component Hantzsch reaction using C-glycosylated reagents. Approach to the asymmetric synthesis of 1,4-diyhydropyridines

Two- and three-component Hantzsch-type cyclocondensation reactions were carried out under thermal conditions using C-glycosylated reagents, namely sugar aldehydes, ketoesters, and enamines. Two different series of 1,4-dihydropyridines bearing C-glycosyl m

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