In this paper, we describe a small library of easy-to-prepare chiral (cyclopentadienone)iron pre-catalysts for enantioselective C[dbnd]O and C[dbnd]N hydrogenations. Starting from readily accessible achiral materials, six chiral (cyclopentadienone)iron complexes (1a-f) possessing a stereogenic plane were synthesized in racemic form. Based on the screening of pre-catalysts (±)-1a-f in the hydrogenation of ketones and ketimines, we selected two complexes (1a and 1d) for resolution by semipreparative enantioselective HPLC. The absolute configuration of the separated enantiomers of 1a and 1d was assigned by XRD analysis (1a) and by comparison between experimental and DFT-calculated ECD and ORD spectra (1d). The enantiopure pre-catalysts (S)-1a and (R)-1d were tested in the asymmetric hydrogenation of several ketones and ketimines and showed good activity and modest enantioselectivity, the e.e. values ranging from very low to moderate (54%).

Chiral (cyclopentadienone)iron complexes with a stereogenic plane as pre-catalysts for the asymmetric hydrogenation of polar double bonds / Bai, Xishan; Cettolin, Mattia; Mazzoccanti, Giulia; Pierini, Marco; Piarulli, Umberto; Colombo, Valentina; Dal Corso, Alberto; Pignataro, Luca; Gennari, Cesare. - In: TETRAHEDRON. - ISSN 0040-4020. - 75:10(2019), pp. 1415-1424. [10.1016/j.tet.2019.01.057]

Chiral (cyclopentadienone)iron complexes with a stereogenic plane as pre-catalysts for the asymmetric hydrogenation of polar double bonds

Mazzoccanti, Giulia;Pierini, Marco;
2019

Abstract

In this paper, we describe a small library of easy-to-prepare chiral (cyclopentadienone)iron pre-catalysts for enantioselective C[dbnd]O and C[dbnd]N hydrogenations. Starting from readily accessible achiral materials, six chiral (cyclopentadienone)iron complexes (1a-f) possessing a stereogenic plane were synthesized in racemic form. Based on the screening of pre-catalysts (±)-1a-f in the hydrogenation of ketones and ketimines, we selected two complexes (1a and 1d) for resolution by semipreparative enantioselective HPLC. The absolute configuration of the separated enantiomers of 1a and 1d was assigned by XRD analysis (1a) and by comparison between experimental and DFT-calculated ECD and ORD spectra (1d). The enantiopure pre-catalysts (S)-1a and (R)-1d were tested in the asymmetric hydrogenation of several ketones and ketimines and showed good activity and modest enantioselectivity, the e.e. values ranging from very low to moderate (54%).
2019
(cyclopentadienone)iron complexes; asymmetric hydrogenation; Iron catalysis; polar double bonds; stereogenic plane; biochemistry; drug discovery3003 pharmaceutical science; organic chemistry
01 Pubblicazione su rivista::01a Articolo in rivista
Chiral (cyclopentadienone)iron complexes with a stereogenic plane as pre-catalysts for the asymmetric hydrogenation of polar double bonds / Bai, Xishan; Cettolin, Mattia; Mazzoccanti, Giulia; Pierini, Marco; Piarulli, Umberto; Colombo, Valentina; Dal Corso, Alberto; Pignataro, Luca; Gennari, Cesare. - In: TETRAHEDRON. - ISSN 0040-4020. - 75:10(2019), pp. 1415-1424. [10.1016/j.tet.2019.01.057]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1245140
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