133797-53-2Relevant academic research and scientific papers
Acid catalyzed ring-opening reactions of optically pure 2-aryl-3,3-dimethyloxetanes
Hu,Kellogg
, p. 1399 - 1408 (2007/10/02)
Some ring-opening reactions of optically pure 2-aryl-3,3-dimethyl oxetanes have been examined under strongly protic or Lewis acid conditions. Ring-opening occurred at the benzylic position and partial inversion of configuration was observed in the case of
Enantioselective aldol chemistry via alkyl enol ethers. Scope of the Lewis acid catalyzed condensation of optically active trimethylsilyl and methyl 2-[(E)-1-alkenyloxy]ethanoates with acetals
Faunce, James A.,Grisso, Bryan A.,Mackenzie, Peter B.
, p. 3418 - 3426 (2007/10/02)
Optically active, mono- and disubstituted trimethylsilyl 2-[(E)-1-alkenyloxy]ethanoates of the type RR1CH = CHOCHR2CO2SiMe3 (R = Me, PhCH2, n-Bu, MeO2CCMe2CH2, PhSCHs
