Bioorthogonal late-stage diversification of amino acids and peptides bears enormous potential for drug discovery and molecular imaging. Despite major accomplishments, these strategies largely rely on traditional, lengthy prefunctionalization methods, heavily involving precious transition-metal catalysis. Herein, we report on a resource-economical manganese(I)-catalyzed C–H fluorescent labeling of structurally complex peptides ensured by direct alkynylation and alkenylation manifolds. This modular strategy sets the stage for unraveling structure-activity relationships between structurally discrete fluorophores towards the rational design of BODIPY fluorogenic probes for real-time analysis of immune cell function.
Transition metal-catalyzed C–H activation has been recognized as a viable strategy in molecular sciences. In contrast, organometallic C–C activation remains relatively scarce. Herein, we report on the control of selectivity...
The chemical up-cycling of polymers into value-added materials offers a unique opportunity to place plastic waste in a new value chain towards a circular economy. Herein, we report the selective...
The use of CO2 as a C1 building block to access carboxylic acids is one of the key aspects in the context of carbon capture and utilization (CCU). Herein we report on an electrochemical carboxylation of allyl esters with CO2 at atmospheric pressure. This strategy enabled to the synthesis of diverse carboxylic acids without the need for a transition metal catalyst. Furthermore, the mechanism was studied through ICP‐MS analysis and cyclic voltammetry studies for the cross ‐electrophile CO2 coupling.
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