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.
Authors
- Gianfranco Favi (ORCID: https://orcid.org/0000-0003-3112-819X)
- Stefania Santeusanio (ORCID: https://orcid.org/0000-0001-7987-5309)
- Giacomo Mari (ORCID: https://orcid.org/0000-0002-5076-942X)
- Lucia De Crescentini (ORCID: https://orcid.org/0000-0002-8239-3340)
- Fabio Mantellini (ORCID: https://orcid.org/0000-0002-1140-5404)
Institutions
- University of Urbino (IT)
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