Cover Feature: Diels‐Alder Reactivity of Triisopropylsilyl Ethynyl Substituted Acenes (Chem. Eur. J. 2/2025)

The Cover Feature shows a sorting box game. The box represents TIPS-pentacene. The shapes of the holes only match with certain building blocks. In the picture, the building blocks represent the dienophiles used. The regioselectivity of the Diels–Alder reaction is determined by the shape of the dienophile blocks. More information can be found in the Research Article by A. Dreuw, J. Freudenberg, U. H. F. Bunz and co-workers (DOI: 10.1002/chem.202403522).

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Publication Details

Journal
Chemistry - A European Journal
Published
2025-01-09
DOI
https://doi.org/10.1002/chem.202580204
Primary Topic
Synthesis and characterization of novel inorganic/organometallic compounds
Type
article
Field-Weighted Citation Impact
0.00
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article

Cover Feature: Diels‐Alder Reactivity of Triisopropylsilyl Ethynyl Substituted Acenes (Chem. Eur. J. 2/2025)

Steffen Maier, Svenja Weigold, Andreas Dreuw, Uwe H. F. Bunz et al.
Chemistry - A European Journal
Synthesis and characterization of novel inorganic/organometallic compounds
article

Cover Feature: Diels‐Alder Reactivity of Triisopropylsilyl Ethynyl Substituted Acenes (Chem. Eur. J. 2/2025)

Steffen Maier, Svenja Weigold, Andreas Dreuw, Uwe H. F. Bunz, Frank Röminger, Fabian Jester, Jan Freudenberg, Tobias Kaczun, Paul Meiners
article en

Abstract

The Cover Feature shows a sorting box game. The box represents TIPS-pentacene. The shapes of the holes only match with certain building blocks. In the picture, the building blocks represent the dienophiles used. The regioselectivity of the Diels–Alder reaction is determined by the shape of the dienophile blocks. More information can be found in the Research Article by A. Dreuw, J. Freudenberg, U. H. F. Bunz and co-workers (DOI: 10.1002/chem.202403522).

Chemistry - A European JournalVol. 31(2)
Heidelberg University (DE)
Openalex Percentile: Top 100%
Synthesis and characterization of novel inorganic/organometallic compounds
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