491869-97-7

Upstream product

• 100-39-0 benzyl bromide 
• 491869-91-1 1,2-O-cyclohexylidene-3,4,5-tri-O-benzyl-6-O-(2-O-benzoyl-3,6-di-O-benzyl-4-O-p-methoxybenzyl-α-D-mannopyranosyl)-D-myo-inositol 
• 727709-38-8 C₆₁H₆₈O₁₂ 
• 491869-83-1 1,2-O-cyclohexylidene-3,4,5-tri-O-benzyl-6-O-(2-O-trifluoromethylsulfonyl-3,6-di-O-benzyl-4-O-p-methoxybenzyl-α-D-mannopyranosyl)-D-myo-inositol 
• 491869-87-5 3,6-di-O-benzyl-4-O-p-methoxybenzyl-β-D-mannopyranose 
• 163039-18-7 (3aS,5R,6S,7S,7aS)-5-Hydroxymethyl-2-pent-4-enyloxy-2-phenyl-tetrahydro-[1,3]dioxolo[4,5-b]pyran-6,7-diol 
• 133162-49-9 1D-3,4,5-tri-O-benzyl-1,2-O-cyclohexylidene-myo-inositol 
• 491869-95-5 1,2-O-cyclohexylidene-3,4,5-tri-O-benzyl-6-O-(2-azido-3,6-di-O-benzyl-2-deoxy-4-O-p-methoxybenzyl-α-D-glucopyranosyl)-D-myo-inositol 

Downstream Products

• 669706-03-0 C₈₇H₉₁N₃O₁₆ 
• 669713-10-4 1,2-O-cyclohexylidene-O-3,4,5-tri-O-benzyl-6-O-{(2-O-benzoyl-3,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-α-D-mannopyranosyl)-(1->4)-O-(2-azido-3,6-di-O-benzyl-2-deoxy-α-D-glucopyranosyl)}-D-myo-inositol 

Relevant academic research and scientific papers

Ytterbium(III) trifluoromethanesulfonate for specific activation of n-pentenyl orthoesters in the presence of acid-sensitive functionalities

Various Lewis acids have been examined as agents which react with N-iodosuccinimide to release iodonium ion for activating n-pentenylorthoester (NPOE) donors, particularly for coupling to acceptors that have acid-labile protecting groups. Although many of

Synthesis of a malaria candidate glycosylphosphatidylinositol (GPI) structure: A strategy for fully inositol acylated and phosphorylated GPIs

A congener of the glycosylphosphatidylinositol (GPI) membrane anchor present on the cell surface of the malaria pathogen Plasmodium falciparum has been synthesized. This GPI is an example of a small number of such membrane anchors that carry a fatty acyl

First synthesis of a malarial prototype: A fully lipidated and phosphorylated GPI membrane anchor

A strategy is described for syntheses of a fully lipidated and phosphorylated prototype of the GPI of Plasmodium falciparum, the causative agent of lethal cerebral, drug-resistant malaria. Orthoesters, prepared in four steps from D-mannose, and methyl α-D