Synthesis of Substituted Resorcinol Monomethyl Ethers from 2-Bromo-3-methoxycyclohex-2-en-1-ones

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dc.contributor.authorShao, Wenjie
dc.contributor.authorClive, Derrick L. J.
dc.date.accessioned2025-05-01T12:11:43Z
dc.date.available2025-05-01T12:11:43Z
dc.date.issued2015-01-01
dc.description2-Bromo-3-methoxycyclohex-2-en-1-ones are readily alkylated at C-6 with reactive halides, and then treatment with DBU (2 equiv) in PhMe at room temperature results in smooth loss of bromide and aromatization to resorcinol (monomethyl ethers of defined substitution pattern.
dc.identifier.doihttps://doi.org/10.7939/r3-75q0-sk96
dc.language.isoen
dc.relation.isversionofShao, W., & Clive, D. L. J. (2016). Synthesis of substituted resorcinol monomethyl ethers from 2-bromo-3-methoxycyclohex-2-en-1-ones. Journal of Organic Chemistry, 80(6), 3211–3216. https://doi-org.login.ezproxy.library.ualberta.ca/10.1021/acs.joc.5b00192
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Journal of Organic Chemistry, copyright © 2015 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.joc.5b02187.
dc.subjectPractical Synthesis
dc.subjectColeophomone-B
dc.subjectInhibitors
dc.subjectOlivetol
dc.subjectAnalogs
dc.subjectAcid
dc.titleSynthesis of Substituted Resorcinol Monomethyl Ethers from 2-Bromo-3-methoxycyclohex-2-en-1-ones
dc.typehttp://purl.org/coar/resource_type/c_6501 http://purl.org/coar/version/c_b1a7d7d4d402bcce http://purl.org/coar/version/c_71e4c1898caa6e32
ual.jupiterAccesshttp://terms.library.ualberta.ca/public

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