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Die enantiospezifische C‐H‐Aktivierung mit einem Ruthenium‐Nanokatalysator ermöglicht die Deuterium‐Markierung von 25 bioaktiven Verbindungen, wie Aminosäuren und Peptiden, mit vollständigem Konfigurationserhalt. In der Zuschrift auf S. 10620 ff. schlagen G. Pieters et al. einen viergliedrigen Dimetallacyclus als Schlüsselintermediat vor und postulieren, dass die kollektive Bewegung von Oberflächenmolekülen...
The activation of CH bonds has revolutionized modern synthetic chemistry. However, no general strategy for enantiospecific CH activation has been developed to date. We herein report an enantiospecific CH activation reaction followed by deuterium incorporation at stereogenic centers. Mechanistic studies suggest that the selectivity for the α‐position of the directing heteroatom results from a four‐membered...
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