Stereochemistry of the reaction of an optically active π-allylpalladium complex with nucleophiles
- 1 January 1984
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 2,p. 107-108
- https://doi.org/10.1039/c39840000107
Abstract
The stereochemistry of the reaction of π-allylpalladium complexes with nucleophiles has been elucidated using optically active (–)-(1S,2R,3R)-di-µ-chloro-bis(1-methyl-3-phenyl-π-allyl)dipalladium(II); dimethyl sodiomalonate and dimethylamine attack a carbon atom of the π-allyl ligand from the side opposite to the palladium (inversion), and phenyl and allyl Grignard reagents attack the π-allyl carbon atom from the same side as the palladium (retention).Keywords
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