Mechanism of asymmetric hydrogenation of ketones catalyzed by BINAP/1,2-diamine-rutheniumII complexes (Q33430487)

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English	Mechanism of asymmetric hydrogenation of ketones catalyzed by BINAP/1,2-diamine-rutheniumII complexes	scientific article

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Europe PubMed Central

26 July 2017

Mechanism of asymmetric hydrogenation of ketones catalyzed by BINAP/1,2-diamine-rutheniumII complexes (English)

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Europe PubMed Central

26 July 2017

Kilian Muñiz

3

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Ryōji Noyori

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4

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Ryoji Noyori

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Europe PubMed Central

26 July 2017

Christian A Sandoval

1

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Europe PubMed Central

PubMed ID

14583046

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26 July 2017

Takeshi Ohkuma

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2

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Europe PubMed Central

PubMed ID

14583046

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26 July 2017

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English

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publication date

1 November 2003

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26 July 2017

Journal of the American Chemical Society

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26 July 2017

125

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44

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26 July 2017

13490-13503

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26 July 2017

Kinetic Resolution of Racemic Secondary Alcohols by RuII-Catalyzed Hydrogen Transfer

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Preparation, x-ray molecular structure, and electronic structure of the first 16-electron ruthenium dihydrogen complexes RuH(H2)X(PCy3)2

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Novel Catalytic Hydrogenolysis of Trimethylsilyl Enol Ethers by the Use of an Acidic Ruthenium Dihydrogen Complex

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Metal-ligand bifunctional catalysis: a nonclassical mechanism for asymmetric hydrogen transfer between alcohols and carbonyl compounds

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CH/pi Attraction: The Origin of Enantioselectivity in Transfer Hydrogenation of Aromatic Carbonyl Compounds Catalyzed by Chiral eta(6)-Arene-Ruthenium(II) Complexes This work was financially supported by a Grant-in-Aid for Scientific Research (No. 0

1 reference

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Transition Metal Polyhydrides: From Qualitative Ideas to Reliable Computational Studies†

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Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones

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Formation of Ruthenium Thiolates via Complexes of Molecular Hydrogen

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Bioreduction of AuCl(4)(-) Ions by the Fungus, Verticillium sp. and Surface Trapping of the Gold Nanoparticles Formed D.M. and S.S. thank the Council of Scientific and Industrial Research (CSIR), Government of India, for financial assistance

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[Nb{B(?6-C6H5)2(C6H5)2}(?2-H3CC2CH3)]: the First Compound with Bent Tetraphenylborate as 12-Electron Donor Ligand

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Catalytic cycle for the asymmetric hydrogenation of prochiral ketones to chiral alcohols: direct hydride and proton transfer from chiral catalysts trans-Ru(H)(2)(diphosphine)(diamine) to ketones and direct addition of dihydrogen to the resulting hyd

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Asymmetric hydrogenation of .beta.-keto carboxylic esters. A practical, purely chemical access to .beta.-hydroxy esters in high enantiomeric purity

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Formation, reactivity, and properties of nondative late transition metal-oxygen and -nitrogen bonds

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Hydride complexes of the transition metals

1 reference

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trans-RuH(eta1-BH4)(binap)(1,2-diamine): a catalyst for asymmetric hydrogenation of simple ketones under base-free conditions

1 reference

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Directionality of Hydrogen Bonds to Sulfur and Oxygen

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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

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Nitroglycal Concatenation: A Broadly Applicable and Efficient Approach to the Synthesis of Complex O-Glycans This work was supported by the Deutsche Forschungsgemeinschaft and the European Community (grant no. FAIR-CT 97-3142). G.A.W. gratefully ack

1 reference

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Mechanism of the hydrogenation of ketones catalyzed by trans-dihydrido(diamine)ruthenium II complexes

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11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA030272C

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DOI

10.1021/JA030272C

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stated in

Europe PubMed Central

26 July 2017

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Europe PubMed Central

PubMed ID

14583046

retrieved

26 July 2017

ResearchGate publication ID

9036583

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Mechanism of asymmetric hydrogenation of ketones catalyzed by BINAP/1,2-diamine-rutheniumII complexes (Q33430487)

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Mechanism of asymmetric hydrogenation of ketones catalyzed by BINAP/1,2-diamine-rutheniumII complexes (Q33430487)

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