Asymmetric iridium-catalyzed hydrogenation of 2-methylindole using phosphite ligands

•Ir-catalyzed asymmetric hydrogenation of 2-methylindole.•Use of monodentate phosphite and amidophosphite ligands.•Use of iodine as the additive resulted in increased enantioselectivity. The iridium-catalyzed asymmetric hydrogenation of 2-methylindole using monodentate phosphites and amidophosphites...

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Veröffentlicht in:Tetrahedron letters 2014-06, Vol.55 (26), p.3613-3614
Hauptverfasser: Lyubimov, Sergey E., Ozolin, Dmitry V., Davankov, Vadim A.
Format: Artikel
Sprache:eng
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Zusammenfassung:•Ir-catalyzed asymmetric hydrogenation of 2-methylindole.•Use of monodentate phosphite and amidophosphite ligands.•Use of iodine as the additive resulted in increased enantioselectivity. The iridium-catalyzed asymmetric hydrogenation of 2-methylindole using monodentate phosphites and amidophosphites as ligands was examined. The use of iodine as the additive resulted in increased enantioselectivity and conversion in the iridium-catalyzed hydrogenation of 2-methylindole. Full conversion and up to 80% ee were obtained with a catalyst based on a phosphite ligand.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2014.04.113