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Oxidative coupling of dichloroaluminium phenolates: Highly selective synthesis of hydroxylated Bi- and tetraaryls

DOI: 10.1016/S0040-4020(01)88316-2

Source and publish data:

Tetrahedron p. 9483 - 9494 (1992)

Update date:2022-08-03

Topics:

Authors:

Sartori, GiovanniSartori, Giovanni

Maggi, RaimondoMaggi, Raimondo

Bigi, FrancaBigi, Franca

Arienti, AttilioArienti, Attilio

Casnati, GiuseppeCasnati, Giuseppe

Bocelli, GabrieleBocelli, Gabriele

Mori, GiovanniMori, Giovanni

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Article abstract of DOI:10.1016/S0040-4020(01)88316-2

Dichloroaluminium phenolates 4 undergo highly selective FeCl3-promoted oxidative coupling. Variously substituted symmetric 2,2′-dihydroxy biaryls 2 are obtained in good yields and excellent selectivities. The chelation control in the final reaction products 7 promotes the chemoselectivity of the process.

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Full text of DOI:10.1016/S0040-4020(01)88316-2

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