287111-22-2

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 5707-04-0 Phenylselenyl chloride 
• 2325-10-2 (S,S)-hydrobenzoin 

Downstream Products

• 1053662-96-6 (2S,3S,4S)-2-((1S,2S)-2-Hydroxy-1,2-diphenyl-ethoxy)-4-phenylselanyl-tetrahydro-pyran-3-ol 
• 287111-31-3 (2S,3R,4S,5S)-2-((1S,2S)-2-Hydroxy-1,2-diphenyl-ethoxy)-tetrahydro-pyran-3,4,5-triol 
• 287111-26-6 (1S,2S)-2-[(1R,2S,6R)-(3,7-Dioxa-bicyclo[4.1.0]hept-2-yl)oxy]-1,2-diphenyl-ethanol 
• 287111-29-9 (2S,3R)-2-((1S,2S)-2-Hydroxy-1,2-diphenyl-ethoxy)-3,6-dihydro-2H-pyran-3-ol 
• 87-72-9 L-(+)-arabinose 
• 287111-24-4 (1S,2S)-2-[(S)-(5,6-Dihydro-2H-pyran-2-yl)oxy]-1,2-diphenyl-ethanol 

Relevant academic research and scientific papers

Enantiopure synthesis of carbohydrates mediated by oxyselenenylation of 3,4-dihydro-2H-pyran

Oxyselenenylation of 3,4-dihydro-2H-pyran with (S,S)hydrobenzoin and subsequent stereoselective transformations afforded the enantiopure L- and D-arabinose while a disaccharide, 6-0-(β-D-arabinopyranosyi)-l,2:3,4-di-Oisopropylidene-a-D-galactopyranose (13) was synthesized from 3,4-dihydro-2H-pyran by utilizing the same methodology.3 The Royal Society of Chemistry 2000.