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 |
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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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