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).

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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
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Front Cover: A Versatile Route to 3,3‐Disubstituded Phthalides Via Arylogous Michael Addition Catalyzed by Organic Base (Adv. Synth. Catal. 20/2025)

J. Thibonnet, Julien Pétrignet, Enzo Eddebbarh, Lou Mazoyer
Advanced Synthesis & Catalysis
Chemical Reactions and Isotopes
article

Front Cover: A Versatile Route to 3,3‐Disubstituded Phthalides Via Arylogous Michael Addition Catalyzed by Organic Base (Adv. Synth. Catal. 20/2025)

J. Thibonnet, Julien Pétrignet, Enzo Eddebbarh, Lou Mazoyer
article en

Abstract

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).

Advanced Synthesis & CatalysisVol. 367(20)
Université de Tours (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR)
Openalex Percentile: Top 75%
Chemical Reactions and Isotopes
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