Betti bases as chiral ligands in the environmentally benign enantioselective transfer hydrogenation

Kóczán Lili and Szőllősi György and Szatmári István: Betti bases as chiral ligands in the environmentally benign enantioselective transfer hydrogenation.

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Abstract

There is a great need for enantioselective synthesis of biological active compounds, since in many cases only one of the stereoisomers can be used as pharmaceutical. Enantioselective transfer hydrogenations of ketones usually catalysed by metal complexes formed with bifunctional ligands, such as 1,2-aminoalcohols, are convenient methods of obtaining chiral alcohols. Our aim was to apply in the enantioselective reduction of a ketone an easily obtained Betti base as chiral ligand, which have not yet been employed in these reactions. During the present study we have obtained complete conversions and high enantioselectivities, up to 96%, in an environmentally friendly aqueous solvent mixture with the simplest Betti base enantiomers prepared from benzaldehyde, ammonia and -naphthol. We hope that our results will pave the way of the application of 1,3-aminohydroxyl derivatives as chiral ligands in other asymmetric catalytic processes as well.

Item Type: Conference or Workshop Item
Journal or Publication Title: Proceedings of the International Symposium on Analytical and Environmental Problems
Date: 2024
Volume: 30
ISBN: 978-963-688-009-5
Page Range: pp. 303-307
Language: English
Publisher: University of Szeged
Place of Publication: Szeged
Event Title: 30th International Symposium on Analytical and Environmental Problems
Event Type: Conference
Event Location: Szeged
Event Dates: 2024. október 7-8.
Related URLs: https://acta.bibl.u-szeged.hu/85607/
Uncontrolled Keywords: Környezetkémia, Gyógyszerkémia
Additional Information: Bibliogr.: 307. p. ; ill. ; összefoglalás angol nyelven
Subjects: 01. Natural sciences
01. Natural sciences > 01.04. Chemical sciences
Date Deposited: 2024. Nov. 26. 12:56
Last Modified: 2024. Nov. 26. 12:56
URI: http://acta.bibl.u-szeged.hu/id/eprint/85745

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