Catalytic highly enantioselective transfer hydrogenation of β-trifluoromethyl nitroalkenes. An easy and general entry to optically active β-trifluoromethyl amines

In the presence of a thiourea catalyst, β-CF3 nitroalkenes react with Hantzsch esters in a highly enantioselective fashion, giving a broad range of β-CF3 amine precursors with a tertiary stereocentre at the β-position. This reaction represents the first general catalytic enantioselective approach to...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2015-01, Vol.51 (4), p.658-660
Hauptverfasser: Martinelli, Emilie, Vicini, Anna Chiara, Mancinelli, Michele, Mazzanti, Andrea, Zani, Paolo, Bernardi, Luca, Fochi, Mariafrancesca
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Sprache:eng
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Zusammenfassung:In the presence of a thiourea catalyst, β-CF3 nitroalkenes react with Hantzsch esters in a highly enantioselective fashion, giving a broad range of β-CF3 amine precursors with a tertiary stereocentre at the β-position. This reaction represents the first general catalytic enantioselective approach to this important class of β-CF3 amines.
ISSN:1359-7345
1364-548X
DOI:10.1039/c4cc07801b