Cover Feature: Formal [2+2+1] Synthesis of Tetrasubstituted Furans from Aldehydes, Acetylenedicarboxylates, and Acyl Compounds (Eur. J. Org. Chem. 33/2019)

The Cover Feature shows the formal [2+2+1] synthesis of tetrasubstituted furans from aldehydes, acetylenedicarboxylates and acyl chlorides or trifluoroacetic anhydride using 4‐picoline and phosphines under the metal‐free and mild conditions. In the present method, 4‐picoline promotes the formation o...

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Veröffentlicht in:European journal of organic chemistry 2019-09, Vol.2019 (33), p.5573-5573
Hauptverfasser: Tateishi, Keiichiro, Matsumoto, Yuri, Saito, Akio
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container_title European journal of organic chemistry
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creator Tateishi, Keiichiro
Matsumoto, Yuri
Saito, Akio
description The Cover Feature shows the formal [2+2+1] synthesis of tetrasubstituted furans from aldehydes, acetylenedicarboxylates and acyl chlorides or trifluoroacetic anhydride using 4‐picoline and phosphines under the metal‐free and mild conditions. In the present method, 4‐picoline promotes the formation of α,β‐enone intermediates from aldehydes and acetylenedicarboxylates followed by the 1,4‐addition (O‐acylation) with acyl compounds and phosphines to give these furan products through an intramolecular Wittig reaction. More information can be found in the Full Paper by A. Saito et al.
doi_str_mv 10.1002/ejoc.201901232
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title Cover Feature: Formal [2+2+1] Synthesis of Tetrasubstituted Furans from Aldehydes, Acetylenedicarboxylates, and Acyl Compounds (Eur. J. Org. Chem. 33/2019)
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