dc.contributor.author | Tsolomitis, A | en |
dc.contributor.author | Sandris, C | en |
dc.date.accessioned | 2014-03-01T01:39:14Z | |
dc.date.available | 2014-03-01T01:39:14Z | |
dc.date.issued | 1987 | en |
dc.identifier.issn | 03855414 | en |
dc.identifier.uri | https://dspace.lib.ntua.gr/xmlui/handle/123456789/22637 | |
dc.relation.uri | http://www.scopus.com/inward/record.url?eid=2-s2.0-0001179080&partnerID=40&md5=6516ea1458f8d0df3e77ac1149eef035 | en |
dc.title | Synthesis of 2-substituted 3(2H)-isothiazolones from 2-substituted 5-aroyl-3(2H)-isothiazolones | en |
heal.type | journalArticle | en |
heal.publicationDate | 1987 | en |
heal.abstract | 2-Substituted 3(2H)-isothiazolones 3 have been prepared from 2-substituted 5-aroyl-3(2H)-isothiazolones 6, which are readily available from N-substituted 3-aroylpropionamides 5. The nucleophilic displacement on the 5-aroyl group was found to proceed easily and quantitatively when a benzene solution of compound 6 was stirred at room temperature either with a 10% sodium hydroxide solution or with solid sodium hydroxide. © 1987. | en |
heal.journalName | Heterocycles | en |
dc.identifier.volume | 25 | en |
dc.identifier.issue | C | en |
dc.identifier.spage | 569 | en |
dc.identifier.epage | 575 | en |
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