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BF3·Et2O controlled reactions of methyl enol ethers: Selective synthesis of dihydrofuro[3,2-c]chromenone and furo[3,2-c]chromenone derivatives
S.A.Z. Ahmad,
Published in Georg Thieme Verlag
2022
Volume: 34
   
Issue: 7
Pages: 823 - 828
Abstract
A facile one-step synthetic approach to dihydrofuro[3,2-c]chromenones and furo[3,2-c]chromenones by the reaction of methyl enol ethers with 4-hydroxy coumarin in a metal-free condition is presented. Dihydrofuro[3,2-c]chromenones and furo[3,2-c]chromenones were selectively obtained by controlling the stoichiometry of boron trifluoride diethyl etherate (BF 3.Et 2O). An unexpected aryl group migration followed by aromatization of furan moiety leading to a variety of furo[3,2-c]chromenone derivatives in good yields is reported. © 2022 Georg Thieme Verlag. All rights reserved.
About the journal
JournalSynlett
PublisherGeorg Thieme Verlag
ISSN09365214
Open AccessNo