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 Photodeconjugation
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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Doi:10.1021/ja01099a060
(1953)Doi:10.1021/jo01120a005
(1955)Doi:10.1021/ol200566s
(2011)Doi:10.1016/j.bmcl.2008.08.106
(2008)Doi:10.1021/jo8021204
(2009)Doi:10.1021/jo802172f
(2009)