Solid‐State Generation of Diarylisonaphthofuran and Its Mechanochemical Diels–Alder Reaction with Epoxynaphthalene

Invited for the cover of this issue are Toshiyuki Hamura and co‐workers at Kwansei Gakuin University. The image depicts solid‐state generation of diarylisonaphthofuran from 1,3‐diaryl‐1,3‐dihydronaphthofuranol and its mechanochemical Diels–Alder reaction with epoxynaphthalene. Read the full text of...

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Published inChemistry : a European journal Vol. 29; no. 69; pp. e202303730 - n/a
Main Authors Wada, Yoshifumi, Tsuchihashi, Keidai, Kanzaki, Masayoshi, Hamura, Toshiyuki
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 11.12.2023
Subjects
Chemistry
Diels-Alder reactions
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Summary:Invited for the cover of this issue are Toshiyuki Hamura and co‐workers at Kwansei Gakuin University. The image depicts solid‐state generation of diarylisonaphthofuran from 1,3‐diaryl‐1,3‐dihydronaphthofuranol and its mechanochemical Diels–Alder reaction with epoxynaphthalene. Read the full text of the article at 10.1002/chem.202302660. “The highly reactive diphenylisonaphthofuran can be safely stored in the solid state, opening new avenues for the use of this attractive quinoidal building block.” This and more about the story behind the front cover can be found in the article at 10.1002/chem.202302660).
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ISSN:0947-6539
1521-3765
DOI:10.1002/chem.202303730