245680-35-7Relevant academic research and scientific papers
Enantioselective synthesis of α-terpineol and nephthenol by intramolecular acyloxazolidinone enolate alkylations
Jin, Yinghua,Coates, Robert M.
, p. 2902 - 2904 (2008/09/18)
Enolate anions generated from norterpenyl bromides bearing oxazolidinone chiral auxiliaries at the chain termini underwent efficient, stereo-biased cyclizations to form 6- and 14-membered rings in novel synthetic routes to α-terpineol and nephthenol enantiomers. The Royal Society of Chemistry 2006.
N-Alkenoylimidazolidin-2-ones as chiral dienophiles in Diels-Alder cycloaddition reactions
Roos, Gregory H. P.,Kriel, Karina N.,Emslie, Neville D.,Balasubramaniam, Sundari
, p. 104 - 112 (2007/10/03)
Homochiral N-enoylimidazolidin-2-ones 5-8 are readily accessible, practical, and highly diastereoselective dienophiles in dialkylaluminium-promoted Diels-Alder reactions. Acrylate, methacrylate, and (E)-crotonate derivatives bearing ephedrine-based imidaz
