Three-component imino Diels–Alder reaction with essential oil and seeds of anise: generation of new tetrahydroquinolines
作者:Vladimir V. Kouznetsov、Arnold R. Romero Bohórquez、Elena E. Stashenko
DOI:10.1016/j.tetlet.2007.10.063
日期:2007.12
A simple and efficient one-pot method for the synthesis of 4-anisyl-2-phenyl-1,2,3,4-tetrahydroquinoline derivatives using a three-component imino Diels–Alder cycloaddition (Povarov reaction) between anilines, benzaldehyde, and trans-anethole in the presence of acidic catalysts is shown. New substituted tetrahydroquinolines are reported and their direct preparation from the anise essential oil is described
PEG-400 as green reaction medium for Lewis acid-promoted cycloaddition reactions with isoeugenol and anethole
作者:Vladimir V. Kouznetsov、Diego R. Merchan Arenas、Arnold R. Romero Bohórquez
DOI:10.1016/j.tetlet.2008.03.049
日期:2008.5
A simple and efficient one-pot method for the synthesis of new 2,4-diaryl-1,2,3,4-tetrahydroquinolines using a three-component imino Diels-Alder cycloaddition between trans-isoeugenol or trans-anethole, anilines, and benzaldehyde in the presence of BF3 center dot OEt2 in PEG-400, a green and reusable solvent, has been developed. Also, BF3 center dot OEt2-catalyzed formal [3+2] cycloaddition reaction of tralls-isoeugenol or trans-anethole with 1,4-benzoquinone in PEG-400 to give dihydrobenzo[b]furan derivatives has been described. (C) 2008 Elsevier Ltd. All rights reserved.