5-phenylpyridazinones - A serendipitous route from coumarins

doi:10.1016/j.tetlet.2008.05.015

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DC 欄位	值	語言
dc.contributor.author	Ghate, Manjunath D.	en_US
dc.contributor.author	Jadhav, Vithal B.	en_US
dc.contributor.author	Shastri, Lokesh A.	en_US
dc.contributor.author	Kulkarni, Manohar V.	en_US
dc.contributor.author	Kulkarni, Geetha M.	en_US
dc.contributor.author	Chen, Chih-Hau	en_US
dc.contributor.author	Sun, Chung-Ming	en_US
dc.date.accessioned	2014-12-08T15:11:12Z	-
dc.date.available	2014-12-08T15:11:12Z	-
dc.date.issued	2008-07-07	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2008.05.015	en_US
dc.identifier.uri	http://hdl.handle.net/11536/8581	-
dc.description.abstract	A new route of the ring transformation has been discovered during the reaction of 4-bromomethylcoumarins with hydrazine hydrate leading to the formation of pharmacologically important pyridazinones in a single step with very high yields. These so obtained pyridazinones have the potential for further functional group interconversions. (C) 2008 Elsevier Ltd. All rights reserved.	en_US
dc.language.iso	en_US	en_US
dc.title	5-phenylpyridazinones - A serendipitous route from coumarins	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/j.tetlet.2008.05.015	en_US
dc.identifier.journal	TETRAHEDRON LETTERS	en_US
dc.citation.volume	49	en_US
dc.citation.issue	28	en_US
dc.citation.spage	4394	en_US
dc.citation.epage	4396	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000257194400020	-
dc.citation.woscount	4	-
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