115901-85-4Relevant academic research and scientific papers
HIGHLY ENANTIOSELECTIVE PROTONATION OF PHOTODIENOLS. AN UNUSUAL SUBSTITUENT EFFECT ON THE INDUCED CHIRALITY
Piva, Olivier,Pete, Jean-Pierre
, p. 5157 - 5160 (2007/10/02)
Enantioselectivities up to 91percent have been reached during the photodeconjugation of α,β-unsaturated esters or lactones using catalytic amounts of new chiral cyclic inductors derived from (+) camphor.Modification of the substitution on the nitrogen of
A VERY ENANTIOSELECTIVE PHOTODECONJUGATION OF α,β-UNSATURATED ESTERS
Piva, Olivier,Henin, Francoise,Muzart, Jacques,Pete, Jean-Pierre
, p. 4825 - 4828 (2007/10/02)
An enantiomer excess up to 70 percent can be obtained in the photodeconjugation of conjugated esters in the presence of (1R, 2S) 1-phenyl, 2-isopropylamino-propanol.
