The discovery of structurally unique scaffolds entities with increased complexity and balanced physicochemical properties has the potential to allow synthetic chemists to exploit areas of chemical space that were previously inaccessible. Among the different strategies employed for generating N-heterocycles, cyclization and cycloaddition reactions represent a valuable synthetic tool. The purpose of this minireview is to summarize the recent advances (2009-present) from our laboratory on the generation of intriguing five-, six- and seven-membered mono- or poly-heterocyclic architectures (linear, fused and spiro) employing 1,2-diaza-1,3-dienes (DDs) as key synthons.
1,2-Diaza-1,3-dienes as a Multifaceted Synthon for the Synthesis of Heterocycles: A Fifteen-Years Update
Lucia De CrescentiniWriting – Original Draft Preparation
;Giacomo MariMembro del Collaboration Group
;Stefania SanteusanioMembro del Collaboration Group
;Gianfranco Favi
Writing – Review & Editing
;Fabio Mantellini
Writing – Review & Editing
In corso di stampa
Abstract
The discovery of structurally unique scaffolds entities with increased complexity and balanced physicochemical properties has the potential to allow synthetic chemists to exploit areas of chemical space that were previously inaccessible. Among the different strategies employed for generating N-heterocycles, cyclization and cycloaddition reactions represent a valuable synthetic tool. The purpose of this minireview is to summarize the recent advances (2009-present) from our laboratory on the generation of intriguing five-, six- and seven-membered mono- or poly-heterocyclic architectures (linear, fused and spiro) employing 1,2-diaza-1,3-dienes (DDs) as key synthons.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
