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Issue 41, 2014
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Molecular iodine-mediated reaction of 2-(2-phenylethynyl)-Morita–Baylis–Hillman adducts: an easy route to naphthyl ketones and iodo-substituted isochromenes

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Abstract

The molecular iodine-promoted reaction of 2-(2-phenylethynyl)-Morita–Baylis–Hillman adducts is reported. In the presence of I2, naphthyl ketone derivatives are produced, whereas in the presence of I2/K3PO4, iodo-substituted isochromene derivatives are produced.

Graphical abstract: Molecular iodine-mediated reaction of 2-(2-phenylethynyl)-Morita–Baylis–Hillman adducts: an easy route to naphthyl ketones and iodo-substituted isochromenes

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Publication details

The article was received on 07 May 2014, accepted on 13 Aug 2014 and first published on 13 Aug 2014


Article type: Paper
DOI: 10.1039/C4OB00938J
Citation: Org. Biomol. Chem., 2014,12, 8247-8256
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    Molecular iodine-mediated reaction of 2-(2-phenylethynyl)-Morita–Baylis–Hillman adducts: an easy route to naphthyl ketones and iodo-substituted isochromenes

    D. Janreddy, V. Kavala, T. Kotipalli, R. R. Rajawinslin, C. Kuo, W. Huang and C. Yao, Org. Biomol. Chem., 2014, 12, 8247
    DOI: 10.1039/C4OB00938J

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