Tetrahedron Letters p. 4825 - 4828 (1987)
Update date:2022-08-15
Topics: Catalyst Enantioselective Stereochemistry Enantiomeric excess Chiral Resolution UV-Vis Spectroscopy Photoisomerization Chirality Quantum Yield α,β-unsaturated esters
Piva, Olivier
Henin, Francoise
Muzart, Jacques
Pete, Jean-Pierre
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.
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