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Dynamic Kinetic Resolution of 2-(Quinolin-8-yl)Benzaldehydes: Atroposelective Iridium-Catalyzed Transfer Hydrogenative Allylation

Authors

CARMONA CARMONA, JOSÉ ALBERTO, Rodriguez-Salamanca, Patricia , Fernandez, Rosario , Lassaletta, Jose M. , Hornillos, Valentin

External publication

Si

Means

Angew. Chem.-Int. Edit.

Scope

Article

Nature

Científica

JCR Quartile

SJR Quartile

JCR Impact

16.1

SJR Impact

5.3

Publication date

28/08/2023

ISI

001029742700001

Abstract

An atroposelective Ir-catalyzed dynamic kinetic resolution (DKR) of 2-(quinolin-8-yl)benzaldehydes/1-naphthaldehydes by transfer hydrogenative coupling of allyl acetate is disclosed. The allylation reaction takes place with simultaneous installation of central and axial chirality, reaching high diastereoselectivities and excellent enantiomeric excesses when ortho-cyclometalated iridium-DM-BINAP is used as the catalyst. The racemization of the substrates occurs through a designed transient Lewis acid-base interaction between the quinoline nitrogen atom and the aldehyde carbonyl group.

Keywords

Allylation; Asymmetric Catalysis; Axial Chirality; Iridium Catalysis; Quinolines

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