95791-15-4

Upstream product

• 111086-99-8 2-(3-Phenylsulfanyl-propoxy)-tetrahydro-pyran 
• 108-98-5 thiophenol 
• 33821-94-2 3-(tetrahydro-2H-pyran-2-yloxy)propyl bromide 
• 873-55-2 sodium benzenesulfonate 

Downstream Products

• 95791-16-5 4-Benzenesulfonyl-1-((4aR,6R,7R,8S,8aR)-7-benzyloxy-8-methoxymethoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-6-(tetrahydro-pyran-2-yloxy)-hexan-3-one 
• 95791-17-6 1-((4aR,6R,7R,8S,8aR)-7-Benzyloxy-8-methoxymethoxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yl)-6-(tetrahydro-pyran-2-yloxy)-hexan-3-one 
• 141502-89-8 [(E)-8-Benzenesulfonyl-2-methylene-10-(tetrahydro-pyran-2-yloxy)-dec-5-enyloxy]-tert-butyl-dimethyl-silane 

Relevant academic research and scientific papers

Tetra-n-butylammonium Oxone. Oxidations under Anhydrous Conditions

Tetra-n-butylammonium Oxone, readily prepared as a white solid from commercially available Oxone, performs oxidations in anhydrous methylene chloride.Under these conditions, sulfides are oxidized to sulfones in the presence of amines, ketones, esters, car

Synthetic studies of marine toxic polyethers. 2. Synthesis of the B-segment of okadaic acid and coupling with the C-segment

Part of okadaic acid was synthesized stereoselectively (involving C-16 through C-38 with 10 asymmetric carbons), by coupling the synthetic segments B and C, the former being prepared from a D-glucopyranose derivative.