1180679-01-9

Upstream product

• 96983-85-6 phenyl 2-phenylethenyl selenide 

Downstream Products

• 1180679-02-0 ethyl 2-cyano-2,3-diphenyl-4-(phenylselenonyl)-butanoate 
• 1235455-29-4 (3aR,7aR)-2-methyl-2-phenylhexahydrobenzo[d][1,3]dioxole 
• 1235572-20-9 C₂₂H₂₀O₂ 
• 141434-77-7 (4R,5R)-2-phenyl-2,4,5-trimethyl-1,3-dioxolane 
• 1235455-22-7 (2R,3R,5R)-2,3-dimethyl-5-phenyl-1,4-dioxane 
• 1235455-11-4 (2R,3R,5S)-2,3-dimethyl-5-phenyl-1,4-dioxane 
• 1235455-26-1 (2R,4aR,8aR)-2-phenyloctahydro-1,4-benzodioxine 
• 1235455-15-8 (2S,4aR,8aR)-2-phenyl-octahydro-1,4-benzodioxine 
• 1235455-19-2 (2R,3R,5R)-2,3,5-triphenyl-1,4-dioxane 
• 1235455-07-8 (2R,3R,5S)-2,3,5-triphenyl-1,4-dioxane 
• 1268165-96-3 (2S,5R)-4-[(4-methylphenyl)sulfonyl]-2,5-diphenylmorpholine 
• 1268165-98-5 (2R,5R)-4-[(4-methylphenyl)sulfonyl]-2,5-diphenylmorpholine 
• 7527-40-4 2-methyl-2-phenylbenzo[d][1,3]dioxole 
• 99783-81-0 2-phenyl-2,3-dihydrobenzo[b][1,4]dioxine 

Relevant academic research and scientific papers

Synthesis of enantiopure 1,4-dioxanes, morpholines, and piperazines from the reaction of chiral 1,2-diols, amino alcohols, and diamines with vinyl selenones

The reactions of readily available vinyl selenones with enantiopure 1,2-diols, N-protected-1,2-aminoalcohols, and diamines gave substituted enantiopure 1,4-dioxanes, morpholines, and piperazines, respectively, in good to excellent yields. The same procedu