Molbank 2010, 2010(2), M678; doi:10.3390/M678
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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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Abstract: 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

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MDPI and ACS Style

Huemer, V.; Holzer, W. 1-Phenylpyrazolo[4',3':5,6]pyrano[3,2-c]pyridine-4(1H)-thione. Molbank 2010, 2010, M678.

AMA Style

Huemer V, Holzer W. 1-Phenylpyrazolo[4',3':5,6]pyrano[3,2-c]pyridine-4(1H)-thione. Molbank. 2010; 2010(2):M678.

Chicago/Turabian Style

Huemer, Valerie; Holzer, Wolfgang. 2010. "1-Phenylpyrazolo[4',3':5,6]pyrano[3,2-c]pyridine-4(1H)-thione." Molbank 2010, no. 2: M678.

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