119238-15-2

Upstream product

• 135214-83-4 1,5-Anhydro-2-deoxy-4,6-O-(phenylmethylene)-D-arabino-hexopyranoside 
• 63554-21-2 (2R,4aR,8aR)-2-Phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one 

Downstream Products

• 119116-55-1 O-(1,5-anhydro-2-deoxy-4,6-O-benzylidene-D-ribohexityl) S-methyl dithiocarbonate 
• 119116-61-9 O-benzyl-enantio-ineupatoriol 
• 119116-57-3 (2R,3S)-3-(benzyloxy)tetrahydropyran-2-carbaldehyde 
• 119116-56-2 (2R,3S)-<3-(benzyloxy)tetrahydropyran-2-yl>methanol 
• 63598-39-0 (2R,4aR,8aS)-2-phenylhexahydropyrano<3,2-d>-1,3-dioxin 
• 843611-69-8 (2S,3S,4R)-4-(4,5-Difluoro-2-methoxy-phenoxy)-2-(di-p-tolyl-phosphinoylmethyl)-tetrahydro-pyran-3-ol 
• 454475-43-5 1,5-anhydro-2,6-dideoxy-3-O-(4,5-difluoro-2-hydroxyphenyl)-6-(diphenylphosphinyl)-D-arabino-hexitol 
• 843609-75-6 (2S,3S,4R)-4-(4,5-Difluoro-2-methoxy-phenoxy)-2-(diphenyl-phosphinoylmethyl)-tetrahydro-pyran-3-ol 
• 850533-42-5 (2S,3S,4R)-2-(Diphenyl-phosphinoylmethyl)-4-(3-methoxy-naphthalen-2-yloxy)-tetrahydro-pyran-3-ol 
• 469911-56-6 4-(di-p-tolyl-phosphinoylmethyl)-tetrahydro-[1,3,2]dioxathiolo[4,5-c]pyran 2,2-dioxide 
• 469911-55-5 (2S,3S,4S)-2-(Di-p-tolyl-phosphinoylmethyl)-tetrahydro-pyran-3,4-diol 
• 469911-54-4 (3aR,4S,7aS)-4-(Diphenyl-phosphinoylmethyl)-tetrahydro-[1,3,2]dioxathiolo[4,5-c]pyran 2,2-dioxide 
• 850533-20-9 Toluene-4-sulfonic acid (2R,3S,4S)-3,4-bis-methoxymethoxy-tetrahydro-pyran-2-ylmethyl ester 
• 291273-51-3 (2S,3S,4R)-2-(Diphenyl-phosphinoylmethyl)-4-(2-hydroxy-phenoxy)-tetrahydro-pyran-3-ol 

Relevant academic research and scientific papers

Practical synthesis of chiral ligands for catalytic enantioselective cyanosilylation of ketones

A practical and more environmentally benign synthetic route of chiral ligands that are useful for catalytic enantioselective cyanosilylation of ketones is described. A key step is the regioselective SN2 reaction to cyclic sulfate 12 with catech

Identifying specific conformations by using a carbohydrate scaffold: Discovery of subtype-selective LPA-receptor agonists and an antagonist

Stable and potent subtype-selective lysophosphatidic acid (LPA) analogues (agonists and an antagonist) were developed by using carbohydrates as a core structure (see scheme). An array of molecules with the recognition motifs of LPA (a phosphate anion, an oleoyl group, and a hydrogen-bond acceptor) attached to carbohydrate isomers in different three-dimensional arrangements were tested for LPA-receptor activation or inhibition. R = alkyl.