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| - videnskabelig artikel (da)
- article científic (ca)
- articolo scientifico (it)
- artigo científico (pt)
- bilimsel makale (tr)
- vedecký článok (sk)
- vetenskaplig artikel (sv)
- vědecký článek (cs)
- wetenschappelijk artikel (nl)
- wissenschaftlicher Artikel (de)
- научни чланак (sr)
- article scientifique (fr)
- artículu científicu espublizáu en 2010 (ast)
- наукова стаття, опублікована в січні 2010 (uk)
- scientific article published on January 2010 (en)
- مقالة علمية نشرت في يناير 2010 (ar)
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| - Mechanism of asymmetric hydrogenation of ketones catalyzed by BINAP/1,2-diamine-rutheniumII complexes
- Transition Metal Polyhydrides: From Qualitative Ideas to Reliable Computational Studies†
- Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones.
- Toward efficient asymmetric hydrogenation: architectural and functional engineering of chiral molecular catalysts
- Mechanism of the hydrogenation of ketones catalyzed by trans-dihydrido(diamine)ruthenium II complexes
- Selective hydrogenation of benzophenones to benzhydrols. Asymmetric synthesis of unsymmetrical diarylmethanols
- General asymmetric hydrogenation of hetero-aromatic ketones
- trans-[RuCl2 (phosphane)2 (1,2-diamine)] and Chiral trans-[RuCl2 (diphosphane)(1,2-diamine)]: Shelf-Stable Precatalysts for the Rapid, Productive, and Stereoselective Hydrogenation of Ketones
- Asymmetric hydrogenation of alpha-chloro aromatic ketones catalyzed by eta6-arene/TsDPEN-ruthenium(II) complexes.
- trans-RuH(eta1-BH4)(binap)(1,2-diamine): a catalyst for asymmetric hydrogenation of simple ketones under base-free conditions
- The hydrogenation/transfer hydrogenation network: asymmetric hydrogenation of ketones with chiral eta6-arene/N-Tosylethylenediamine-ruthenium(II) catalysts
- Asymmetric hydrogenation of alpha-hydroxy ketones catalyzed by MsDPEN-Cp*Ir(III) complex.
- Synthesis and antimuscarinic properties of quinuclidin-3-yl 1,2,3,4-tetrahydroisoquinoline-2-carboxylate derivatives as novel muscarinic receptor antagonists
- Asymmetric hydrogenation of aromatic ketones catalyzed by the TolBINAP/DMAPEN-ruthenium(II) complex: a significant effect of N-substituents of chiral 1,2-diamine ligands on enantioselectivity
- Asymmetric hydrogenation of tert-alkyl ketones
- Highly enantioselective hydrogenation of aryl vinyl ketones to allylic alcohols catalyzed by the tol-binap/dmapen ruthenium(II) complex.
- BINAP/1,4-diamine-ruthenium(II) complexes for efficient asymmetric hydrogenation of 1-tetralones and analogues
- Asymmetric hydrogenation of aromatic, aliphatic, and alpha,beta-unsaturated acyl silanes catalyzed by Tol-binap/Pica ruthenium(II) complexes: practical synthesis of optically active alpha-hydroxysilanes.
- Metal-ligand bifunctional catalysis for asymmetric hydrogenation.
- General asymmetric hydrogenation of alpha-branched aromatic ketones catalyzed by TolBINAP/DMAPEN-ruthenium(II) complex.
- Mechanism of asymmetric hydrogenation of acetophenone catalyzed by chiral eta(6)-arene-N-tosylethylenediamine-ruthenium(II) complexes
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| - Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (en)
- Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (nl)
- Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (ast)
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| skos:prefLabel
| - Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (en)
- Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (nl)
- Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (ast)
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| name
| - Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (en)
- Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (nl)
- Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (ast)
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| title
| - Asymmetric hydrogenation of ketones: tactics to achieve high reactivity, enantioselectivity, and wide scope (en)
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