Literature DB >> 18543261

The major/minor concept: dependence of the selectivity of homogeneously catalyzed reactions on reactivity ratio and concentration ratio of the intermediates.

Thomas Schmidt1, Zhenya Dai, Hans-Joachim Drexler, Marko Hapke, Angelika Preetz, Detlef Heller.   

Abstract

The homogeneously catalyzed asymmetric hydrogenation of prochiral olefins with cationic Rh(I) complexes is one of the best-understood selection processes. For some of the catalyst/substrate complexes, experimental proof points out the validation of the major/minor principle; the concentration-deficient minor substrate complex, which has very high reactivity, yields the excess enantiomer. As exemplified by the reaction system of [Rh(dipamp)(MeOH)2]+/methyl (Z)-alpha-acetamidocinnamate (dipamp=1,2-bis((o-methoxyphenyl)phenylphosphino)ethane), all six of the characteristic reaction rate constants have been previously identified. Recently, it was found that the major substrate complex can also yield the major enantiomer (lock-and-key principle). The differential equation system that results from the reaction sequence can be solved numerically for different hydrogen partial pressures by including the known equilibrium constants. The result displays the concentration-time dependence of all species that exist in the catalytic cycle. On the basis of the known constants as well as further experimental evidence, this work focuses on the examination of all principal possibilities resulting from the reaction sequence and leading to different results for the stereochemical outcome. From the simulation, the following conclusions can be drawn: 1) When an intermediate has extreme reactivity, its stationary concentration can become so small that it can no longer be the source of product selectivity; 2) in principle, the major/minor and lock-and-key principles can coexist depending on the applied pressure; 3) thermodynamically determined intermediate ratios can be completely converted under reaction conditions for a selection process; and 4) the increase in enantioselectivity with increasing hydrogen partial pressure, a phenomenon that is experimentally proven but theoretically far from being well-understood, can be explained by applying both the lock-and-key as well as the major/minor principle.

Entities:  

Year:  2008        PMID: 18543261     DOI: 10.1002/asia.200800023

Source DB:  PubMed          Journal:  Chem Asian J        ISSN: 1861-471X


  2 in total

1.  Combined Theoretical and Experimental Studies Unravel Multiple Pathways to Convergent Asymmetric Hydrogenation of Enamides.

Authors:  Jianping Yang; Luca Massaro; Suppachai Krajangsri; Thishana Singh; Hao Su; Emanuele Silvi; Sudipta Ponra; Lars Eriksson; Mårten S G Ahlquist; Pher G Andersson
Journal:  J Am Chem Soc       Date:  2021-12-14       Impact factor: 15.419

2.  Size is Important: Artificial Catalyst Mimics Behavior of Natural Enzymes.

Authors:  Jianzhong Chen; Ilya D Gridnev
Journal:  iScience       Date:  2020-03-05
  2 in total

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