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Application of the anionic homologous Fries rearrangement to the synthesis of 3-alkylbenzofuran-2(3H)-ones

Azzena, Ugo Gavino and Pisano, Luisa and Pittalis, Mario (2009) Application of the anionic homologous Fries rearrangement to the synthesis of 3-alkylbenzofuran-2(3H)-ones. ChemInform, Vol. 40 (1). eISSN 1522-2667. Article.

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DOI: 10.1002/chin.200901109

Abstract

The substrates (I) and (VII), generated via Fries rearrangement according to the known procedure, are subjected to metalation and electrophilic trapping [cf. (III)] followed by acidic cyclization to yield the desired benzofuran derivatives.

Item Type:Article
ID Code:1518
Status:Published
Refereed:Yes
Uncontrolled Keywords:Benzofuran derivatives, ring closure reactions, C-C bond formation
Subjects:Area 03 - Scienze chimiche > CHIM/06 Chimica organica
Divisions:001 Università di Sassari > 01 Dipartimenti > Chimica
Publisher:Wiley
eISSN:1522-2667
Deposited On:18 Aug 2009 10:05

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