Monatshefte fur Chemie p. 1161 - 1168 (1988)
Update date:2022-08-04
Topics:
Brunner, Henri
Kraus, Joerg
Lautenschlager, Hans-Juergen
Chiral enamines, obtained by Schiff base condensation from 1,3-dicarbonyl compounds and (R)-(+)-1-phenylethylamine, were found to undergo diastereoselective Michael reactions with α,β-unsaturated carbonyl compounds.After removal of the chiral auxiliary (R
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