Base-Mediated One-pot Synthesis of Oxygen-Based Heterocycles from 2-Hydroxyphenyl-Substituted para-Quinone Methides

dc.contributor.authorSingh, Gurpreet
dc.contributor.authorKumar, Suresh
dc.contributor.authorChowdhury, Arjun
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-11-27T09:42:16Z
dc.date.available2020-11-27T09:42:16Z
dc.date.issued2019
dc.description.abstractOne-pot synthesis of oxygen-containing heterocycles has been achieved through alkylation/acylation of 2-hydroxyphenyl-substituted para-quinone methides followed by an intramolecular 1,6-conjugate addition/cyclization and oxidation sequence. This protocol provides access to a wide range of oxygen-based heterocycles, such as 2,3-disubstituted benzo[b]furans, 2,3-dihydrobenzofurans and diaryl-substituted coumarin derivatives in moderate to good yields.en_US
dc.identifier.citationJournal of Organic Chemistry, 84(24),pp. 15978–15989.en_US
dc.identifier.otherhttps://doi.org/10.1021/acs.joc.9b02455
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/acs.joc.9b02455
dc.identifier.urihttp://hdl.handle.net/123456789/2341
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectOxygenen_US
dc.subjectHeterocyclesen_US
dc.subjectSynthesisen_US
dc.titleBase-Mediated One-pot Synthesis of Oxygen-Based Heterocycles from 2-Hydroxyphenyl-Substituted para-Quinone Methidesen_US
dc.typeArticleen_US

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