720698-25-9

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 7103-29-9 1,2-dideoxy-D-allose 
• 135214-83-4 1,5-Anhydro-2-deoxy-4,6-O-(phenylmethylene)-D-arabino-hexopyranoside 
• 2873-29-2 D-glucal triacetate 
• 13035-12-6 3,4,6-tri-O-acetyl-1,2-dideoxy-D-glucopyranose 
• 3971-47-9 (3S,4R)-dihydroxy-(2R)-(hydroxymethyl)tetrahydropyran 
• 13035-13-7 4,6-O-benzylidene-1,2-dideoxy-D-glucose 
• 63554-21-2 (2R,4aR,8aR)-2-Phenyl-tetrahydro-pyrano[3,2-d][1,3]dioxin-8-one 
• 119238-15-2 1,5-anhydro-2-deoxy-4,6-O-benzylidene-D-ribohexitol 

Downstream Products

• 469911-53-3 2-(diphenylphosphinoylmethyl)tetrahydropyran-3,4-diol 
• 53951-42-1 (2R)-2r-Methyl-tetrahydro-pyran-3t,4t-diol 
• 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 
• 291273-51-3 (2S,3S,4R)-2-(Diphenyl-phosphinoylmethyl)-4-(2-hydroxy-phenoxy)-tetrahydro-pyran-3-ol 
• 469911-57-7 (2S,3S,4R)-2-(Diphenyl-phosphinoylmethyl)-4-(2-methoxy-phenoxy)-tetrahydro-pyran-3-ol 
• 850533-20-9 Toluene-4-sulfonic acid (2R,3S,4S)-3,4-bis-methoxymethoxy-tetrahydro-pyran-2-ylmethyl ester 

Relevant academic research and scientific papers

Synthesis and inhibitory activity of deoxy-d-allose amide derivative against plant growth

1,2,6-Trideoxy-6-amido-d-allose derivative was synthesized and found to exhibit higher growth-inhibitory activity against plants than the corresponding deoxy-d-allose ester, which indicates that an amide group at C-6 of the deoxy-d-allose amide enhances i

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

Biomimetic cyclisation of prebrevetoxin polyepoxide models

(E)-1,3-Dihydroxyhex-4-ene and (E)-1,3-dihydroxy-4-methylhex-4-ene undergo epoxidation with peracetic acid and in situ cyclisation to give a mixture of tetrahydro-furans and -pyrans, whereas comparable compounds lacking the allylic hydroxyl group give pre