Acid-Induced Rearrangement of Cycloadducts from Cyclopropenecarboxylates and 1,3-Diarylisobenzofurans

Treatment of several Diels–Alder adducts of cyclopropenecarboxylates and 1,3‐diarylisobenzofurans with a strong acid triggers a skeletal rearrangement resulting in 4,8b‐dihydro‐3aH‐indeno[1,2‐b]furans.

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Veröffentlicht in:Helvetica chimica acta 2016-07, Vol.99 (7), p.487-493
Hauptverfasser: Efremova, Mariia M., Molchanov, Alexander P., Larina, Anna G., Starova, Galina L., Kostikov, Rafael R., Stepakov, Alexander V.
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container_end_page 493
container_issue 7
container_start_page 487
container_title Helvetica chimica acta
container_volume 99
creator Efremova, Mariia M.
Molchanov, Alexander P.
Larina, Anna G.
Starova, Galina L.
Kostikov, Rafael R.
Stepakov, Alexander V.
description Treatment of several Diels–Alder adducts of cyclopropenecarboxylates and 1,3‐diarylisobenzofurans with a strong acid triggers a skeletal rearrangement resulting in 4,8b‐dihydro‐3aH‐indeno[1,2‐b]furans.
doi_str_mv 10.1002/hlca.201500114
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subjects 1,3‐Diarylisobenzofurans
2-b]furans
3-Diarylisobenzofurans
Cyclopropenecarboxylates
Diels-Alder adduct
Indeno
Indeno[1,2‐b]furans
Rearrangements
title Acid-Induced Rearrangement of Cycloadducts from Cyclopropenecarboxylates and 1,3-Diarylisobenzofurans
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