Switchover of the Diastereofacial Selectivity in the Michael Reaction of a Chiral Ester Enolate with a,a-Enone

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Synlett | / 9卷 / 827期

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[31] THE DIASTEREOSELECTIVE SYNTHESIS OF ESTER-FUNCTIONALIZED ALKENES THROUGH THE STEREOCONTROLLED CONJUGATE ADDITION (MICHAEL REACTION) OF PROCHIRAL ENOLATES TO CHIRAL ALPHA-METHYLENE BETA-LACTONES AND THERMAL DECARBOXYLATION OF THE RESULTING ALPHA-SUBSTITUTED BETA-LACTONES
SALGADO, VON
PETERS, EM
PETERS, K
VONSCHNERING, HG
ADAM, W
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (12): : 3879 - 3886

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