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Molbank 2010, 2010(2), M678; doi:10.3390/M678
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 and *
Department of Drug and Natural Product Synthesis, Faculty of Life Sciences, University of Vienna, Althanstrasse 14, A-1090 Vienna, Austria
* Author to whom correspondence should be addressed.
Received: 29 March 2010 / Accepted: 23 April 2010 / Published: 26 April 2010
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The title compound is prepared by treatment of 1-phenylpyrazolo[4',3':5,6]pyrano[3,2-c]pyridin-4(1H)-one with Lawesson’s reagent in refluxing toluene. Detailed spectroscopic data (1H NMR, 13C NMR, 15N NMR, MS) are presented.
Keywords: phenylpyrazolo[4',3':5,6]pyrano[3,2-c]pyridine-4(1H)-thiones; Lawesson’s reagent; thionation; NMR phenylpyrazolo[4',3':5,6]pyrano[3,2-c]pyridine-4(1H)-thiones; Lawesson’s reagent; thionation; NMR
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Huemer, V.; Holzer, W. 1-Phenylpyrazolo[4',3':5,6]pyrano[3,2-c]pyridine-4(1H)-thione. Molbank 2010, 2010, M678.

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