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