Front Cover: A Versatile Route to 3,3‐Disubstituded Phthalides Via Arylogous Michael Addition Catalyzed by Organic Base (Adv. Synth. Catal. 20/2025)
Arylogous Michael Additions The cover art, designed by Enzo Eddebbarh and Julien Petrignet, depicts a chef in a laboratory coat preparing a tomato sauce to represent a Michael adduct by combining simple ingredients: an arylphthalide and a Michael acceptor. The simplicity of the transformation is emphasized by the mild reaction conditions: acetonitrile and a pinch of DBU. The ease with which the product is formed mirrors the effortless preparation of a chef’s sauce and demonstrates compatibility with a broad range of substrates and reflecting the gram-scale feasibility. More information can be found in the Research Article by Julien Petrignet and co-workers (10.1002/adsc.70128).
Authors
- J. Thibonnet (ORCID: https://orcid.org/0000-0003-3817-210X)
- Julien Pétrignet (ORCID: https://orcid.org/0000-0003-3328-601X)
- Enzo Eddebbarh
- Lou Mazoyer
Institutions
- Université de Tours (FR)
- Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR)
Publication Details
- Journal
- Advanced Synthesis & Catalysis
- Published
- 2025-10-29
- DOI
- https://doi.org/10.1002/adsc.70181
- Primary Topic
- Chemical Reactions and Isotopes
- Type
- article
- Field-Weighted Citation Impact
- 0.00