Abstract
A high regioselectivity has been observed in the palladium catalyzed allylation of "soft" nucleophiles (pentane-2,4-dione and 4-hydroxy-6-methyl-2-pyrone) when both allylic termini have the same steric requirements and different electronic features. © 1989.
Original language | English |
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Pages (from-to) | 3109-3112 |
Journal | Tetrahedron Letters |
Volume | 30 |
Issue number | 23 |
DOIs | |
Publication status | Published - 1 Jan 1989 |