8 Papers
27 Citations
Ru Jiang is an academic researcher from Fourth Military Medical University. The author has contributed to research in topics: Enantioselective synthesis & Asymmetric hydrogenation. The author has an hindex of 4, co-authored 8 publications.
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Papers
Ferrocene as a Privileged Framework for Chiral Organocatalysts
TL;DR: Ferrocene (Fc) as a privileged framework for chiral organocatalysts (Orgcat) has been developed rapidly in recent years as discussed by the authors, and five categories of them including Fc-based nucleophilic, bifunctional, Bronsted acid, hydrogen-bonding and frustrated Lewis pairs were summarized.
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Highly Regio- and Enantioselective Hydrogenation of Conjugated α-Substituted Dienoic Acids
Xian Liu,Song Liu,Quanjun Wang,Gang Zhou,Lin Yao,Qin Ouyang,Ru Jiang,Yu Lan,Yu Lan,Weiping Chen +9 more
TL;DR: Highly regio- and enantioselective hydrogenation of conjugated α-substituted dienoic acids was realized for the first time using Trifer-Rh complex, providing a straightforward method for the synthesis of chiral α- substituted γ,δ-unsaturated acids.
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Ferrocenophane-based bifunctional organocatalyst for highly enantioselective Michael reactions
TL;DR: Highly enantioselective Michael reactions between acetylacetone and trans-β-nitroolefins are achieved by a novel ferrocenophane-based tertiary amine-thiourea organocatalyst to provide the corresponding products in good to excellent yields and enantiOSElectivities.
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Ferrocene-based bifunctional organocatalyst for highly enantioselective intramolecular Rauhut–Currier reaction
TL;DR: In this article, three series of novel ferrocene-based bifunctional chiral phosphines have been designed and synthesized, and they showed good performance in enantioselective intramolecular Rauhut-Currier reaction of bis(enones), giving the corresponding products in good yield with up to 98% ee.
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Iridium-Catalyzed Asymmetric Hydrogenation of Sterically Hindered Cyclic Imines for Enantioselective Synthesis of Tetrahydroisoquinolines.
Bin Li,Ruixia Liu,Jing Yang,Jingyuan Luo,Lin Yao,Muqiong Li,Xiaohui Zheng,Ru Jiang,Huifang Nie,Shengyong Zhang,Shengyong Zhang +10 more
TL;DR: In this paper, an efficient enantioselective hydrogenation of sterically hindered cyclic imines catalyzed by the Ir-tBu-ax-Josiphos complex has been described, producing a series of useful chiral bulky tetrahydroisoquinoline analogs in high isolated yields (85-96%) with good to excellent enantiorelectivities (74-99% ee).
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