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Excellent catalyst precursor in terms of ease of activation to form a variety of catalysts with the
aid of various chiral/achiral ligands.
Solubility: Soluble in THF, Toluene, Pentane
Molecular Formula: C16H26Ru
Molecular Weight: 319.5
CAS: 12289-94-0 |

Ru-124 |
Applications
Stereoselective anti-Markovnikov-Addition to Alkynes
An in situ catalyst system generated from Ru(Me-allyl)2(COD) with a phosphine ligand was found to efficiently catalyze addition of thioamides to terminal alkynes with exclusive formation of the anti-Markovnikov thioenamide products
L. J. Goossen, M. Blancho, K. S. Salih, R. Karch, A. Rivas-Nass Org. Lett., 2008, 10, 4497
Enantioselective hydrogention of α,ß unsaturated acids
A useful catalyst precursor for making chiral bisphosphine based Ru acetate or trifluoroacteate catalysts, for example [Ru(COD)(CF3COO2]/ R-Xyl PhanePhos, a highly active and efficient catalytic system for the hydrogenation of an unsaturated acid.
G.A.Grasa, A.Zanotti-Gerosa, S. Ghosh, G.A.Teleha, W.A.Kinney, B.E.Maryanoff, Tet. Lett. 2008, 49, 5328
Enantioselective Hydrogenation of C=C double bonds in N-Boc-pyrroles
The first reported successful enantioselective hydrogenation of a pyrrole
R. Kuwano, M. Kashiwabara, M. Ohsumi, H. Kusano J. Am. Chem. Soc., 2008, 130, 808
Hydrogenation of cyclic or acyclic β-(acylamino)crylates
Ru(Me-allyl)2(COD) in conjunction with chiral biaryl ligands provides an efficient catalytic method for the synthesis of both cis and trans chiral cyclic β- amino acid derivatives.
W. Tang, S. Wu, X. Zhang J. Am. Chem. Soc., 2003, 125, 9570
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