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Org Lett ; 24(13): 2573-2578, 2022 04 08.
Artigo em Inglês | MEDLINE | ID: mdl-35348342

RESUMO

The synergistic chiral Lewis acid/achiral Pd catalyst system was successfully applied in the enantioselective benzylation of various imine esters, giving a range of α-benzyl-substituted α-amino acid derivatives in satisfactory yield with excellent enantioselectivity. It is worth noting that this strategy exhibits good tolerance for bicyclic and monocyclic benzylic electrophiles. Furthermore, the utility of this synthetic protocol was demonstrated by the expedient preparation of enantioenriched antihypertensive drug α-methyl-l-dopa.


Assuntos
Ácidos de Lewis , Paládio , Aminoácidos , Compostos Azo , Catálise , Paládio/química , Estereoisomerismo , Tiossemicarbazonas
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