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• W2178856593 startingPage "1347" @default.
• W2178856593 abstract "The electrophilic cyclization of substituted propargylic aryl ethers by I2, ICl, and PhSeBr produces 3,4-disubstituted 2H-benzopyrans in excellent yields. This methodology results in vinylic halides or selenides under mild reaction conditions and tolerates a variety of functional groups, including methoxy, alcohol, aldehyde, and nitro groups." @default.
• W2178856593 created "2016-06-24" @default.
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• W2178856593 date "2007-01-13" @default.
• W2178856593 modified "2023-10-02" @default.
• W2178856593 title "Synthesis of 3,4-Disubstituted 2<i>H</i>-Benzopyrans through C−C Bond Formation via Electrophilic Cyclization" @default.
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• W2178856593 doi "https://doi.org/10.1021/jo062234s" @default.
• W2178856593 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2527782" @default.
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