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• W2473725905 endingPage "10233" @default.
• W2473725905 startingPage "10226" @default.
• W2473725905 abstract "A new version of benzannulation featuring the use of aromatic tert-butyl ynol ethers as the convenient precursors for arylketenes has been developed. Both ynamides and ynol ethers undergo this reaction smoothly, giving 3-amino and 3-alkoxy 1-naphthols in good to excellent yields under the heated reaction conditions. The high efficiency, excellent regioselectivity, good functional group compatibility, and broad substrate scope render this reaction particularly valuable for organic synthesis." @default.
• W2473725905 created "2016-07-22" @default.
• W2473725905 creator A5043719260 @default.
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• W2473725905 date "2015-09-25" @default.
• W2473725905 modified "2023-10-17" @default.
• W2473725905 title "Construction of 1-Naphthols via Benzannulation Based on the Reaction of Aryl <i>tert</i>-Butyl Ynol Ethers with Ynamides or Ynol Ethers" @default.
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• W2473725905 doi "https://doi.org/10.1021/acs.joc.5b01858" @default.
• W2473725905 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26389568" @default.
• W2473725905 hasPublicationYear "2015" @default.
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