233744-17-7

Upstream product

• 233744-16-6 [(2R,3R,4S,5R,6S)-3,4-Bis-benzyloxy-6-methoxy-5-(4-nitro-benzyloxy)-tetrahydro-pyran-2-yl]-methanol 

Downstream Products

• 233744-18-8 4-[4-((2S,3R,4S,5R,6R)-4,5-Bis-benzyloxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yloxymethyl)-phenylcarbamoyl]-butyric acid 
• 57783-73-0 methyl 3,4-di-O-benzyl-α-D-glucopyranoside 
• 350671-48-6 4-[4-((2S,3R,4S,5R,6R)-4,5-Bis-benzyloxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-3-yloxymethyl)-phenylcarbamoyl]-butyric acid 4-(5-ethyl-2,4,6-trioxo-hexahydro-pyrimidin-5-ylmethyl)-benzyl ester 

Relevant academic research and scientific papers

Synthesis based on affinity separation (SAS): Separation of products having barbituric acid tag from untagged compounds by using hydrogen bond interaction

A new method is described for affinity purification of synthetic compounds based on molecular recognition between bis(2,6-diaminopyridine)amide of isophthalic acid and a barbituric acid derivative. The desired compounds possessing the barbituric acid deri

A novel oxidatively removable linker and its application to α-selective solid-phase oligosaccharide synthesis on a macroporous polystyrene support

A novel p-acylaminobenzyl-type linker and its application to the solid phase synthesis of oligosaccharides are described. The p-glutarylaminobenzyl ether of a monosaccharide was readily introduced to a polymer support by amide bond formation. The linker moiety was smoothly cleaved by DDQ oxidation. α-Selective glycosylation was accomplished by virtue of the solvent effect of diethyl ether on a solid support of a macroporous polystyrene. High α-selectivity was achieved by the use of benzylated donors possessing the bulky t-butyldiphenylsilyl group at the 6-position.