1,2‐Diaza‐1,3‐Dienes as a Multifaceted Synthons for the Synthesis of Heterocycles: A Fifteen‐Years Update

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.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-08-09
DOI
https://doi.org/10.1002/ejoc.202400716
Citations
8
Primary Topic
Cyclopropane Reaction Mechanisms
Type
article
Field-Weighted Citation Impact
2.00
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article

1,2‐Diaza‐1,3‐Dienes as a Multifaceted Synthons for the Synthesis of Heterocycles: A Fifteen‐Years Update

Gianfranco Favi, Stefania Santeusanio, Giacomo Mari, Lucia De Crescentini et al.
8 citations
European Journal of Organic Chemistry
Cyclopropane Reaction Mechanisms
2.00
article

1,2‐Diaza‐1,3‐Dienes as a Multifaceted Synthons for the Synthesis of Heterocycles: A Fifteen‐Years Update

Gianfranco Favi, Stefania Santeusanio, Giacomo Mari, Lucia De Crescentini, Fabio Mantellini
article en
8 citations

Abstract

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.

European Journal of Organic ChemistryVol. 27(44)
University of Urbino (IT)
Openalex Percentile: Top 14%
Cyclopropane Reaction Mechanisms
2.00
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