Cover Feature: Visible Light Promoted Site‐Specific Functionalization of α‐Acyloxy Carboxamides: Unlocking a Forbidden Chemical Space in the Passerini Reaction (Chem. Eur. J. 50/2024)
Transforming the impossible into the possible: A chemical astronaut exploits blue light irradiation to activate Passerini products containing a Hantzsch ester. This modern method facilitates the generation of α-acyloxyamide radicals, which can be trapped by suitable Michael acceptors, enabling the exploration of a novel chemical space. The new Passerini products obtained formally derive from “impossible aldehydes”. More information can be found in the Research Article by G. Papeo, G. C. Tron and co-workers (DOI: 10.1002/chem.202402175).
Authors
- Maurizio Pulici (ORCID: https://orcid.org/0000-0001-5142-5760)
- Francesca Brunelli (ORCID: https://orcid.org/0000-0001-8396-5745)
- Francesca Quartieri (ORCID: https://orcid.org/0000-0002-7438-5981)
- Gianluca Papeo (ORCID: https://orcid.org/0000-0002-4773-4437)
- Ivana Miletto (ORCID: https://orcid.org/0000-0002-0313-7614)
- Gian Cesare Tron (ORCID: https://orcid.org/0000-0002-2394-400X)
Institutions
- Università degli Studi del Piemonte Orientale “Amedeo Avogadro” (IT)
- Nerviano Medical Sciences (IT)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2024-09-05
- DOI
- https://doi.org/10.1002/chem.202485004
- Primary Topic
- Microbial Metabolism and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00