Issue 41, 2017

Tetrasubstituted cyclopentadienones as suitable enantiopure ligands with axial chirality

Abstract

A series of thermally stable atropisomeric phencyclone ligands (ΔGrac > 35 kcal mol−1), bearing two chiral axes, has been successfully synthesized, taking into account the results of DFT calculations on model systems. The absolute configurations of the novel atropisomers have been assigned using TD-DFT simulation of ECD spectra. Atropisomeric phencyclones herein presented pave the way towards new ruthenium-based enantioselective hydrogenation catalysts.

Graphical abstract: Tetrasubstituted cyclopentadienones as suitable enantiopure ligands with axial chirality

Supplementary files

Article information

Article type
Paper
Submitted
15 Jun 2017
Accepted
11 Sep 2017
First published
11 Sep 2017

Org. Biomol. Chem., 2017,15, 8720-8728

Tetrasubstituted cyclopentadienones as suitable enantiopure ligands with axial chirality

L. Prati, M. Mancinelli, A. Ciogli and A. Mazzanti, Org. Biomol. Chem., 2017, 15, 8720 DOI: 10.1039/C7OB01455D

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