368452-29-3

Upstream product

• 201232-73-7 p-tert-butylphenyl 4,6-di-O-tert-butyl(dimethyl)silyl-2,3-dideoxy-α-D-erythro-hex-2-enopyranoside 
• 201232-87-3 [4,6-di-O-(tert-butyldimethylsilyl)-2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl]benzene 
• 368452-23-7 (2,3-dideoxy-β-D-erythro-hex-2-enopyranosyl)benzene 

Relevant academic research and scientific papers

Enantiopure trioxadecalin derived liquid crystals: Influence of phenyl substitution on the mesogenic properties

Nickel(0)-catalyzed reaction of pseudo-glucal 1 with Grignard reagents derived from bromobenzene and 1-bromo-4-phenylbenzene gives the corresponding β-C-aryl glycosides 2. Desilylation and hydrogenation of 2 leads to saturated β-C-aryl glycosides 4, which

Synthesis and Mesogenic Properties of Enantiopure Trioxadecalin Derivatives Bearing a n-Alkylphenyl Substituent

Reaction of pseudo-glucal 1 with Grignard reagents derived from various 4-n-alkyl-4-bromobenzene in the presence of a catalytic amount of NiCl2(dppe), gives the corresponding unsaturated β-C-aryl glycosides 2. Desilylation and hydrogenation of these compo