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

email
Published: 22 March 2000
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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.
PDF Full-text Download PDF Full-Text [17 KB, uploaded 18 June 2014 19:25 CEST]

Export to BibTeX |
EndNote


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