Abstract
The reactivity in the confined spaces of zeolites, metal-organic frameworks, cage compounds and macrocycles differ in many aspects from those conducted in bulk solution. Cases of altered regioselectivity, enhanced stability and accelerated substrate reactivity are presented within the context of non-covalent interactions between host and guest molecules, which define much of supramolecular chemistry, being unique and imparting highly useful properties that are of interest for their intellectual merit as well as their immense commercial value.
Keywords: Catalysis, metal-organic frameworks, supramolecular, zeolite.
Graphical Abstract
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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