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Zinc-Chloride-Promoted Domino Reaction of Phenols with Terminal Alkynes under Solvent-Free Conditions: An Efficient Synthesis of Chromenes
C. Sreenivasulu,
Published in Wiley-VCH Verlag
2018
Volume: 2018
   
Issue: 22
Pages: 2846 - 2857
Abstract
A domino one-pot synthesis of 2H-chromenes and 4H-chromenes starting from phenols and terminal acetylenes in an atom economical reaction under solvent-free conditions is described. This annulation reaction between phenols with alkynes is promoted by the simple Lewis acid ZnCl2. Significantly, to the best of our knowledge, the synthesis of 2H-chromenes is the first of its kind, as it is based on the use of terminal alkyl acetylenes. The described method shows a broad substrate scope and good functional group tolerance. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
About the journal
JournalData powered by TypesetEuropean Journal of Organic Chemistry
PublisherData powered by TypesetWiley-VCH Verlag
ISSN1434193X