Tetrahedron Letters p. 3291 - 3294 (1998)
Update date:2022-07-29
Topics:
Bolzacchini, Ezio
Brunow, Gosta
Meinardi, Simone
Orlandi, Marco
Rindone, Bruno
Rummakko, Petteri
Setala, Harri
The first stereoselective free radical coupling of a phenylpropenoidic phenolic compound is reported. The oxidation of a chiral ferulic acid amide to give dimeric benzofuranic neolignan is performed enzymatically using horseradish peroxidase as the catalyst. Enantiomeric excess in a biologically active compound with phenylcoumaran skeleton (β-5 dimer) is thus obtained.
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