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Lithium perchlorate accelerated Friedel–Crafts addition of furans to β-nitrostyrenes
Authors:Martin J Stoermer  Hans-Matthias Richter  Dieter E Kaufmann
Institution:1. Division of Chemistry and Structural Biology, Institute for Molecular Bioscience, University of Queensland, St. Lucia, Queensland 4072, Australia;2. Institut für Organische Chemie der Technischen Universität Clausthal, D-38678 Clausthal-Zellerfeld, Germany
Abstract:The Friedel–Crafts alkylation of furans by the Michael acceptor, β-nitrostyrene, is greatly accelerated by the use of the Lewis acid catalyst and solvent, 5 M lithium perchlorate in diethyl ether (LDPE).
Keywords:YLQBMQCUIZJEEH-UHFFFAOYSA-N  PIAOLBVUVDXHHL-VOTSOKGWSA-N  LXSVNNJQGACXKY-UHFFFAOYSA-N  YSGMDHJSEPHJEL-UHFFFAOYSA-N  XNZFTYWHFUCLED-UHFFFAOYSA-N  XAXQKORTXNWPKU-UHFFFAOYSA-N  KZZWETBWQYVSNG-UHFFFAOYSA-N  SFDZQDSRANYBDR-UHFFFAOYSA-N  FFRJUXQEQIGPOT-UHFFFAOYSA-N  KTPMXTMSEBTWLL-UHFFFAOYSA-N  GMRNPXSSMGHQLW-UHFFFAOYSA-N  SAGXPOQKYBFZEA-UHFFFAOYSA-N
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