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

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

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
PDF Full-text Download PDF Full-Text [17 KB, uploaded 20 November 2008 08:41 CET]
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.

Article Statistics

Load and display the download statistics.

Citations to this Article

Cite This Article

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.

Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert