Atroposelective Synthesis of 2-(Quinolin-8-yl)benzyl Alcohols by Biocatalytic Dynamic Kinetic Resolutions

A highly enantioselective biocatalytic dynamic kinetic resolution (DKR) of 2-(quinoline-8-yl) 3-methylbenzaldehydes and 1-naphthaldehydes is described. The reaction proceeds by atroposelective carbonyl reduction catalyzed by commercial ketoreductases (KREDs), generally reaching high conversions and...

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Detalles Bibliográficos
Autores: Coto-Cid, Juan M., de Gonzalo, Gonzalo, Carmona, José A., Iglesias-Sigüenza, Javier, Rodríguez-Salamanca, Patricia, Fernández, Rosario, Hornillos, Valentín, Lassaletta, José M.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2024
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/356103
Acceso en línea:http://hdl.handle.net/10261/356103
https://api.elsevier.com/content/abstract/scopus_id/85181742989
Access Level:acceso abierto
Palabra clave:Asymmetric catalysis
Axial chirality
Dynamic kinetic resolution
Ketoreductases
Quinolines
Descripción
Sumario:A highly enantioselective biocatalytic dynamic kinetic resolution (DKR) of 2-(quinoline-8-yl) 3-methylbenzaldehydes and 1-naphthaldehydes is described. The reaction proceeds by atroposelective carbonyl reduction catalyzed by commercial ketoreductases (KREDs), generally reaching high conversions and excellent enantiomeric excesses. Both atropoisomers of the final alcohols can be obtained by a proper selection of the biocatalyst. The DKR strategy relies in the racemization of the stereogenic axis that takes place thanks to a transient Lewis acid-base interaction (LABI) between the nitrogen in the quinoline and the carbonyl group.