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Cover Feature: Monohydride‐Dichloro Rhodium(III) Complexes with Chiral Diphosphine Ligands as Catalysts for Asymmetric Hydrogenation of Olefinic Substrates (Chem. Eur. J. 40/2020)

Kosuke Higashida, Fabian Brüning, Nagataka Tsujimoto, Kenya Higashihara, Haruki Nagae, Antonio Togni, Kazushi Mashima

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Abstract

Monohydride-dichloro rhodium(III) complexes bearing chiral diphosphine ligands stand as novel candidates for asymmetric hydrogenation of non-functionalized olefins. The sterically hindered chiral diphosphine ligand, (S)-DTBM-SEGPHOS, made it possible to isolate the rhodium(III) complex as a mononuclear complex which was confirmed by XRD analysis and DOSY NMR analysis. The novel monohydride rhodium(III) complex showed much higher enantioselectivity than classical dihydride rhodium systems on asymmetric hydrogenation of non-functionalized olefins. More information can be found in the Full Paper by A. Togni, K. Mashima, et al. on page 8749.

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Monohydride-dichloro rhodium(III) complexes bearing chiral diphosphine ligands stand as novel candidates for asymmetric hydrogenation of non-functionalized olefins. The sterically hindered chiral diphosphine ligand, (S)-DTBM-SEGPHOS, made it possible to isolate the rhodium(III) complex as a mononuclear complex which was confirmed by XRD analysis and DOSY NMR analysis. The novel monohydride rhodium(III) complex showed much higher enantioselectivity than classical dihydride rhodium systems on asymmetric hydrogenation of non-functionalized olefins. More information can be found in the Full Paper by A. Togni, K. Mashima, et al. on page 8749.

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Available abstract

Monohydride-dichloro rhodium(III) complexes bearing chiral diphosphine ligands stand as novel candidates for asymmetric hydrogenation of non-functionalized olefins. The sterically hindered chiral diphosphine ligand, (S)-DTBM-SEGPHOS, made it possible to isolate the rhodium(III) complex as a mononuclear complex which was confirmed by XRD analysis and DOSY NMR analysis. The novel monohydride rhodium(III) complex showed much higher enantioselectivity than classical dihydride rhodium systems on asymmetric hydrogenation of non-functionalized olefins. More information can be found in the Full Paper by A. Togni, K. Mashima, et al. on page 8749.

Key concepts: Rhodium, Asymmetric hydrogenation, Steric effects, Chemistry, Catalysis, Ligand (biochemistry), Medicinal chemistry, Stereochemistry

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Cover Feature: Monohydride‐Dichloro Rhodium(III) Complexes with Chiral Diphosphine Ligands as Catalysts for Asymmetric Hydrogenation of Olefinic Substrates (Chem. Eur. J. 40/2020) — Research Paper | ScholarLens