Abstract
A survey is provided on new synthetic pathways to pyrido[1,2-a]pyrimidinium, pyrido[1,2-a]pyrazinium, pyrido[1,2-c]pyrimidinium, and pyrido[1,2-b]pyridazinium systems and their partially saturated derivatives appeared during the recent years. Reaction mechanisms of these ring closure methodologies are also discussed. Some representative further transformations of these ring systems are also summarized. Thus, alkylation of olates and thiolates, ring opening reactions, photochemical transformations and flash vacuum pyrolytic reactions are reviewed.
Keywords: Claisen condensation, Stille-coupling, alkylating reagent, zwitterionic aziniumolates, quinolizinium cation, Bridgehead-nitrogen
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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