5-phenylpyridazinones - A serendipitous route from coumarins
| dc.citation.epage | 4396 | en_US |
| dc.citation.issue | 28 | en_US |
| dc.citation.spage | 4394 | en_US |
| dc.citation.volume | 49 | en_US |
| dc.citation.woscount | 4 | |
| 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.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | 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.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.identifier.doi | 10.1016/j.tetlet.2008.05.015 | en_US |
| dc.identifier.issn | 0040-4039 | en_US |
| dc.identifier.journal | TETRAHEDRON LETTERS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/j.tetlet.2008.05.015 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/8581 | |
| dc.identifier.wosnumber | WOS:000257194400020 | |
| dc.language.iso | en_US | en_US |
| dc.title | 5-phenylpyridazinones - A serendipitous route from coumarins | en_US |
| dc.type | Article | en_US |