741685-92-7

Upstream product

• 58479-61-1 tert-butylchlorodiphenylsilane 
• 741685-83-6 ethyl (3R,4S,5R,6R,7R)-3-(allylamino)-4,5,6-tris(benzyloxy)-7,8-dihydroxyoctanoate 

Downstream Products

• 741686-00-0 ethyl (3R,4S,5R,6R,7R)-3-{allyl[(9H-fluoren-9-yl)methoxycarbonyl]amino}-4,5,6-tris(benzyloxy)-8-[(tert-butyldiphenylsilyl)oxy]-7-hydroxyoctanoate 
• 1054797-32-8 3-[allyl-(9H-fluoren-9-ylmethoxycarbonyl)-amino]-4,5,6-tris-benzyloxy-8-(tert-butyl-diphenyl-silanyloxy)-7-oxo-octanoic acid ethyl ester 
• 741686-07-7 ethyl [(2R,3S,4R,5R,6R)-1-allyl-3,4,5-tris(benzyloxy)-6-{[(tert-butyldiphenylsilyl)oxy]methyl}piperidin-2-yl]acetate 
• 741686-18-0 ethyl [(2R,3S,4R,5R,6R)-1-allyl-3,4,5-tris(benzyloxy)-6-(hydroxymethyl)piperidin-2-yl]acetate 
• 741686-22-6 [(2R,3S,4R,5R,6R)-1-allyl-3,4,5-tris(benzyloxy)-6-(hydroxymethyl)piperidin-2-yl]acetic acid 
• 741686-28-2 ethyl [(2R,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(hydroxymethyl)piperidin-2-yl]acetate 

Relevant academic research and scientific papers

Synthesis of imino sugar scaffolds for the generation of glycosidase inhibitor libraries

We have synthesized imino sugar scaffolds bearing two points of diversity - the stereocenters located in α positions relative to the nitrogen atom - and three points of orthogonal derivatization - a carboxylic function, the primary hydroxy group, and the