Tandem mass spectrometric study of annelation isomers of the novel thieno[3',2':4,5]pyrido[2,3-d]pyridazine ring system

dc.contributor.author	Krajsovszky, Gábor
dc.contributor.author	Tóth, Eszter
dc.contributor.author	Ludányi, Krisztina
dc.date.accessioned	2015-09-14T17:08:59Z
dc.date.available	2015-09-14T17:08:59Z
dc.date.issued	2014
dc.identifier	84905576413
dc.identifier.citation	pagination=158-169; journalVolume=2014; journalIssueNumber=5; journalTitle=ARKIVOC;
dc.identifier.uri	http://repo.lib.semmelweis.hu//handle/123456789/2165
dc.description.abstract	In the present communication, we describe tandem combinations of Suzuki - condensation ring closure reactions to obtain a novel thieno[3 -,2 -:4,5]pyrido[2,3-d]pyridazine ring system. These compounds were studied by tandem mass spectrometry in detail and characteristic fragmentations were observed, which can be useful to confirm the presence of N -substituted pyridazine ring in synthesized compounds. © ARKAT-USA,Inc.
dc.relation.ispartof	urn:issn:1551-7004
dc.title	Tandem mass spectrometric study of annelation isomers of the novel thieno[3',2':4,5]pyrido[2,3-d]pyridazine ring system
dc.type	Journal Article
dc.date.updated	2015-09-11T09:14:44Z
dc.language.rfc3066	en
dc.identifier.mtmt	2788938
dc.identifier.wos	000345779400010
dc.contributor.department	SE/GYTK/Szerves Vegytani Intézet
dc.contributor.department	SE/GYTK/Gyógyszerészeti Intézet
dc.contributor.institution	Semmelweis Egyetem
dc.contributor.institution	Semmelweis Egyetem