Abstract
The classical redox chemistry of the NADH-NAD+ cofactors and their synthetic analogues (dihydropyridines and pyridinium salts) has been extended to non-biomimetic processes. These involve reactions that bypass the electron transfer processes and allow the functionalization of the heterocyclic parent systems with a broad variety of carbon- and heteroatom-based functional groups. The scope of the methodology, and its applications to organic synthesis are analyzed.
Keywords: redox chemistry, dihydropyridines, pyridinium salts, non-biomimetic
Call for Papers in Thematic Issues
Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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