172748-82-2Relevant academic research and scientific papers
Asymmetric synthesis using C2-symmetric diols: Use of (5R,6R)-3-acetoxy-5,6-diphenyl-1,4-dioxan-2-one as a chiral synthetic equivalent of 1,2-ethanediol 1,2-dicarbocation
Fujioka,Matsunaga,Kitagawa,Nagatomi,Kondo,Kita
, p. 2117 - 2120 (1995)
A new route to chiral diol systems has been developed based on double nucleophilic addition to the cationic ions fixed on a 6-membered ring system using chiral hydrobenzoin as an auxiliary.
Asymmetric synthesis using C2-symmetric diols: Use of (5R,6R)-2,3-diacetoxy-5,6-diphenyl-1,4-dioxane as a chiral synthesis equivalent of 1,2-ethanediol 1,2-dicarbocation
Fujioka,Kitagawa,Nagatomi,Kita
, p. 2113 - 2116 (1995)
A new route to chiral diol systems has been developed based on the double nucleophilic addition to (5R,6R)-2,3-diacetoxy-5,6-diphenyl-1,4-dioxanes using chiral hydrobenzoin as an auxiliary.
