51224-10-3

Upstream product

• 51224-09-0 6-(2,2,2-trifluoroacetamido)hexyl 4-methylbenzenesulfonate 
• 40248-34-8 6-trifluoroacetamido-1-hexanol 
• 4048-33-3 6-amino-1-hexanol 

Downstream Products

• 1613232-74-8 C₃₈H₅₃NO₇S 
• 1422975-14-1 C₃₇H₅₇NO₇S 
• 51224-17-0 N-[(2S,3R,4R,5S,6R)-2-(6-Amino-hexylsulfanyl)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yl]-acetamide 
• 51224-14-7 (2S,3R,4S,5R,6R)-2-(6-Amino-hexylsulfanyl)-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 
• 912641-65-7 5'-O-(4,4'-dimethoxytrityl)-N⁶-(2-phenoxyacetyl)-2'-O-(6-trifluoroacetamido)hexyladenosine 
• 912641-63-5 N⁶-(2-phenoxyacetyl)-2'-O-(6-trifluoroacetamido)hexyladenosine 
• 912641-74-8 5'-O-(4,4'-dimethoxytrityl)-2'-O-(6-trifluoroacetamido)hexyluridine 

Relevant academic research and scientific papers

PROCESS OF MAKING PROSTACYCLIN COMPOUNDS WITH LINKER THIOL AND PEGYLATED FORMS

A process provides for producing chiral prostacyclin derivatives of Formula (I) in high yield from meso anhydrides.

Zwitterionic oligonucleotides: A study on binding properties of 2′-O-aminohexyl modifications

2′-O-Aminohexyl side chains provide excellent conditions for zwitterionic interstrand and intrastrand interactions of oligonucleotides. 2′-O-Aminoalkylated phosphoramidites of adenosine and undine were synthesized and incorporated in increasing number int

PREPARATION OF ANOMERIC PAIRS OF 1-THIOGLYCOSIDES: USE OF ANOMERIZATION CATALYZED BY BORON TRIFLUORIDE

Anomeric pairs of some alkyl 1-thioaldopyranosides of D-galactose, D-glucose, D-mannose, 2-acetamido-2-deoxy-D-glucose, 2-acetamido-2-deoxy-D-galactose, and L-fucose were prepared.The per-O-acetylated, 1,2-trans anomers of 6-(trifluoroacetamido)hexyl 1-thioaldopyranosides and 5-(methoxycarbonyl)pentyl 1-thioaldopyranosides were anomerized with boron trifluoride in dichloromethane.The anomeric mixtures were then separated by chromatography, using columns of either silica gel or an ion-exchange resin.De-blocking of the separated compounds provided pure anomers of 6-aminohexyl 1-thioaldopyranosides or 5-carboxypentyl 1-thioaldopyranosides.The aglycons of the latter glycosides were further extended by reaction with aminoacetaldehyde diethyl acetal, which, after deacetalization of the products, provided an ω-aldehydo group.These series of glycosides could be readily coupled to proteins or solid matrices.