Artificial enzymes for the enantioselective Michael-type addition of thiols combining basic catalysis with two- and three-pronged oxyanion hole mimics

Simona, Luis; Muniz, Francisco M.; Saez, Silvia; Raposo, Cesar; Moran, Joaquin R.

Abstract

Artificial receptors with catalytic activities have been obtained for the enantioselective conjugated addition of ethanethiol to 5,6-dihydro-2-(H)-pyridinone. The xanthone-based receptors include an oxyanion hole structure combined with amine groups. Computer modeling studies have been performed on the reaction mechanism in an attempt to explain the catalytic activity.

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Título según WOS: ID WOS:000249059300005 Not found in local WOS DB
Título de la Revista: ARKIVOC
Editorial: ARKAT USA INC
Fecha de publicación: 2007
Página de inicio: 47
Página final: 64
DOI:

10.3998/ark.5550190.0008.405

Notas: ISI