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dc.contributor.authorChen, Li-Hsunen_US
dc.contributor.authorXu, Zhan-Huien_US
dc.contributor.authorLin, Chun-Chungen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2014-12-08T15:29:09Z-
dc.date.available2014-12-08T15:29:09Z-
dc.date.issued2013-02-06en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tetlet.2012.11.012en_US
dc.identifier.urihttp://hdl.handle.net/11536/21017-
dc.description.abstractIonic liquid supported synthesis of guanidine linked piperazine, diazepane, and aminomethylpiperidine to difluoroquinoxalinones and difluoro benzodiamine was achieved by two regioisomeric products. They were isolated from one pot reduction and intramolecular cyclization to afford quinoxalinone ring system with traceless cleavage of ionic liquid support. Besides, the ionic-supported other isomer was further cleaved in methanol. All the reactions were carried out on an ionic liquid support under various conditions to deliver biologically relevant scaffolds with high purity and excellent yields. (C) 2012 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectIonic liquid supporten_US
dc.subjectMicrowave synthesisen_US
dc.subjectOne-Bead-Two-Compounden_US
dc.subjectQuinoxalinonesen_US
dc.titleDivergent ionic liquid supported synthesis of isolable guanidine linked quinoxalinone and benzodiamineen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2012.11.012en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.citation.volume54en_US
dc.citation.issue6en_US
dc.citation.spage454en_US
dc.citation.epage458en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000314388300002-
dc.citation.woscount1-
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