Transition-Metal-Containing Chiral Bidentate Ligands for Enantioselective Catalysis: Non-Metallocene Architectural Units Come of Age

ChemInform ◽  
2003 ◽  
Vol 34 (25) ◽  
Author(s):  
Olivier Delacroix ◽  
John A. Gladysz
1985 ◽  
Vol 40 (10) ◽  
pp. 1243-1249 ◽  
Author(s):  
Henri Brunner ◽  
Alfons Knott

The chelate phosphanes Diphos, Diop, and Norphos were reacted with C5H5Mn(CO)2THF and CH3C5H4Mn(CO)2THF to give mononuclear complexes, containing the phosphanes as unidentate or as bidentate ligands, and dinuclear complexes, containing bridging phosphane ligands. In C5H5Mn(CO)2Diop one of the two P(C6H5)2 groups of Diop is coordinated to the C5H5Mn(CO)2 fragment; the uncoordinated P(C6H5)2 group makes it a monodentate ligand. C5H5Mn(CO)2Diop together with [Rh(cod)Cl]2 was used as an in situ catalyst in the enantioselective hydrogenation of (Z)-a-[N -acetam ino]cinnamic acid (78.4% ee) and in the enantioselective hydrosilylation of acetophenone with diphenylsilane (6.7% ee).


1983 ◽  
Vol 38 (5) ◽  
pp. 587-591 ◽  
Author(s):  
Alexander Filippou ◽  
Ernst Otto Fischer

AbstractReaction of trans-bromotetracarbonyl(phenylcarbyne)-complexes of chromium, molybdenum and tungsten and trans-bromotetracarbonyl(methylcarbyne) complexes of chromium and tungsten with the bidentate ligands 2,2′-bipyridyl and 1,10-phenanthroline results in the replacement of two carbonyl groups leading to very thermostable carbyne complexes with the general formula Br(CO)2LMCR (L: 2,2′-bipy, ophen; M: Cr, Mo, W; R : CH3, C6H5).


2015 ◽  
Vol 16 (12) ◽  
pp. 11034-11054 ◽  
Author(s):  
Enis Md Yusof ◽  
Thahira Ravoof ◽  
Edward Tiekink ◽  
Abhimanyu Veerakumarasivam ◽  
Karen Crouse ◽  
...  

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