All articles of this category A marked advancement of reactivity and enantioselectivity in palladium-catalyzed asymmetric allylations was achieved by variations of electronic substituent effects in a new series of chiral P-N hybrid ligands 1 . The first evident observation demonstrates that the introduction of electron-donating groups is effective to improve the catalytic performance in the allylic transformation. chiral P-N hydrid ligand - electronic substituent effect - electron-donating group - palladium catalyst - asymmetric allylation
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Saitoh et al. (1999) studied this question.
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