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Palladium(0)-catalyzed asymmetric C(sp3)-H arylation using a chiral binol-derived phosphate and an achiral ligand.


ABSTRACT: The first efficient palladium(0)-catalyzed enantioselective C(sp3)-H activation reaction using a catalytic chiral base and an achiral phosphine ligand is reported. Fine-tuning the binol-derived phosphoric acid pre-catalyst and the reaction conditions was found to be crucial to achieve high levels of enantioselectivity for a variety of indoline products containing both tri- and tetrasubstituted stereocenters.

SUBMITTER: Yang L 

PROVIDER: S-EPMC5360168 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

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Palladium(0)-catalyzed asymmetric C(sp<sup>3</sup>)-H arylation using a chiral binol-derived phosphate and an achiral ligand.

Yang Lei L   Melot Romain R   Neuburger Markus M   Baudoin Olivier O  

Chemical science 20161011 2


The first efficient palladium(0)-catalyzed enantioselective C(sp<sup>3</sup>)-H activation reaction using a catalytic chiral base and an achiral phosphine ligand is reported. Fine-tuning the binol-derived phosphoric acid pre-catalyst and the reaction conditions was found to be crucial to achieve high levels of enantioselectivity for a variety of indoline products containing both tri- and tetrasubstituted stereocenters. ...[more]

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