Synthesis of Optically Active Michael Adducts Via Chiral Enamines

DOI: 10.1007/BF00809268

Source and publish data:

Monatshefte fur Chemie p. 1161 - 1168 (1988)

Update date:2022-08-04

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Authors:

Brunner, Henri

Kraus, Joerg

Lautenschlager, Hans-Juergen

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Article abstract of DOI:10.1007/BF00809268

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

Full text of DOI:10.1007/BF00809268

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