The AlCl3–L Reagent and its Application to the Regioselective Carbon–Carbon Bond Formation

doi:10.3390/50300319

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Molecules 2000, 5(3), 319-320; doi:10.3390/50300319

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The AlCl3–L Reagent and its Application to the Regioselective Carbon–Carbon Bond Formation

Alejandra G. Suárez

Instituto de Química Orgánica de Síntesis - IQUIOS, CONICET. Facultad de Ciencias Bioquímicas y Farmacéuticas - Universidad Nacional de Rosario. Suipacha 531, 2000 Rosario, Argentina

Published: 22 March 2000

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Abstract: Use of the AlCl₃–L reagent in the regioselective acylation of benzodioxinic derivatives. Spectroscopic studies show the presence of coordination compounds as reaction intermediates, being the responsible of the observed regioselectivity.

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MDPI and ACS Style

Suárez, A.G. The AlCl3–L Reagent and its Application to the Regioselective Carbon–Carbon Bond Formation. Molecules 2000, 5, 319-320.

AMA Style

Suárez AG. The AlCl3–L Reagent and its Application to the Regioselective Carbon–Carbon Bond Formation. Molecules. 2000; 5(3):319-320.

Chicago/Turabian Style

Suárez, Alejandra G. 2000. "The AlCl3–L Reagent and its Application to the Regioselective Carbon–Carbon Bond Formation." Molecules 5, no. 3: 319-320.

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