Cluster-Based Catalytic Hydrogenation with High Conversion and Reversible Enantioselectivity-Reference-Cited by-同舟云学术

Cluster-Based Catalytic Hydrogenation with High Conversion and Reversible Enantioselectivity

Published:2000-12-01 Issue:26 Volume:19 Page:5568-5574
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Homanen Pertti¹,Persson Roger¹,Haukka Matti¹,Pakkanen Tapani A.¹,Nordlander Ebbe¹

Affiliation:

1. Inorganic Chemistry 1, Chemical Center, Lund University, Box 124, SE-221 00 Lund, Sweden, and Department of Chemistry, University of Joensuu, Box 111, FIN-80101 Joensuu, Finland

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om000367c

Reference29 articles.

1. (b) Gladfelter, W. L.; Roesselet, K. J. InThe Chemistry of Metal Cluster Complexes; Shriver, D. F., Kaesz, H. D., Adams, R. D., Eds.; VCH: Weinheim, 1990; pp 329−365.

2. Synthesis and structural characterization of the tetraruthenium cluster complexes [Ru4(µ-H)4(CO)10(L–L)](L–L = diphosphine)

3. Interaction of dodecacarbonyltetra-.mu.-hydridotetraruthenium with diphosphines in the presence of trimethylamine N-oxide. X-ray crystal structure analyses of (.mu.-H)4Ru4(CO)10(.mu.-{Ph2P(CH2)nPPh2}) (n = 1, 3, 4), (.mu.-H)4Ru4(CO)10(.mu.-{Ph2PCH2CH(CH3)PPh2}), and (.mu.-H)4Ru4(CO)10({Ph2PCH2CH(CH3)PPh2})

4. Asymmetric homogeneous catalysis by ruthenium complexes

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