Preparation and lithiation of optically active 2,2'-dihalo-1,1'-binaphthyls. A general strategy for obtaining chiral, bidentate ligands for use in asymmetric synthesis

1984 ◽  
Vol 106 (17) ◽  
pp. 4717-4723 ◽  
Author(s):  
Kenneth J. Brown ◽  
Matthew S. Berry ◽  
Kenneth C. Waterman ◽  
David Lingenfelter ◽  
Joseph R. Murdoch
2015 ◽  
Vol 51 (2) ◽  
pp. 380-383 ◽  
Author(s):  
Masahiro Egi ◽  
Kaori Shimizu ◽  
Marin Kamiya ◽  
Yuya Ota ◽  
Shuji Akai

An asymmetric synthesis of highly substituted indenes has been developed via the central–axial–central chirality transfer from optically active propargyl alcohols.


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).


2010 ◽  
Vol 91 (7) ◽  
pp. 861-868 ◽  
Author(s):  
W. M. B. Könst ◽  
W. N. Speckamp ◽  
H. O. Houwen ◽  
H. O. Huisman

1980 ◽  
Vol 333 (1 Transition Me) ◽  
pp. 35-44 ◽  
Author(s):  
J. K. Stille ◽  
S. J. Fritschel ◽  
N. Takaishi ◽  
T. Masuda ◽  
H. Imai ◽  
...  

1988 ◽  
Vol 52 (12) ◽  
pp. 3087-3092 ◽  
Author(s):  
Yukio YAMAMOTO ◽  
Kazuyoshi YAMAMOTO ◽  
Takaaki NISHIOKA ◽  
Jun''ichi ODA

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