Axial chiral compounds hydrogenation

Arylation, olefins, 187, 190 Arylketimines, iridium hydrogenation, 83 Arylpropanoic acid, Grignard coupling, 190 Aspartame, 8, 27 Asymmetric catalysis characteristics, 11 chiral metal complexes, 122 covalently bound intermediates, 323 electrochemistry, 342 hydrogen-bonded associates, 328 industrial applications, 8, 357 optically active compounds, 2 phase-transfer reactions, 333 photochemistry, 341 polymerization, 174, 332 purely organic compounds, 323 see also specific complexes Asymmetric induction, 71, 155 Attractive interaction, 196, 216 Autoinduction, 330 Axial chirality, 18 Aza-Diels-Alder reaction, 220 Azetidinone, 44, 80 Aziridination, olefins, 207... 

A column loaded with the amide 58 that is held in place merely by hydrogen bonds and electrostatic forces is used preparatively to resolve the important axially chiral binaphthol13 59. You will meet compounds of this type as reagents and ligands in chiral catalysts in chapters 24-26. 

The first place in catalytic hydrogenation nowadays is taken by Rh or Ru complexes of BINAP. This ligand has axial chirality as the naphthalene rings cannot rotate past each other. These compounds were developed by Noyori, who with Knowles and Sharpless received the 2001 Nobel prize for their contributions to asymmetric synthesis. BINAP 20 is usually made from BINOL 19 and either 19 or 20 can be resolved. Rhodium complexes similar to those we have met include a molecule of cyclooctadiene and, as these are Rh(I) compounds, a counterion, often triflate 21. Both enantiomers of BINAP are available commercially.8... 

The axial chirality is the consequence of two perpendicular planes associated with the R2 and hydrogen substituents on the C-4 carbon atom of the cyclohexyl ring and the alkene substituents, R, and H this is more clearly seen in Fig. 7 (b). The optically active compounds were obtained by a series of elegant stereoselective reactions, outlined in Scheme 9. 

Bidentate Phosphorus Ligands Supported on Atropisomeric Biaryl Backbones. Most ligands of this group contain binaphthyl or biphenyl moieties-providing an axial element of chirality. The flagship of this class of compounds is the atropisomeric diphosphane BINAP (36), whose complexes (primarily Ru(II) complexes (37)) play a pivotal role in asymmetric scale-up hydrogenations and isomerizations (Fig. 5). 

Mainly (i ) Deuterium compounds with axial or planar chirality, (ii) Chirality due to isotopes of atoms other than hydrogen. (See also Z5 l)... 

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