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dc.contributor.authorWu, CHen_US
dc.contributor.authorSun, CMen_US
dc.date.accessioned2014-12-08T15:16:51Z-
dc.date.available2014-12-08T15:16:51Z-
dc.date.issued2006-04-10en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.tetlet.2006.02.015en_US
dc.identifier.urihttp://hdl.handle.net/11536/12384-
dc.description.abstractA multistep liquid phase synthesis of specifically functionalized bis-benzimidazoles is presented by the application of single-mode microwave irradiation technique. The sustained solubilizing power and stability of the PEG-ester derived from the commercially available 4-fluoro-3-nitrobenzoic acid has been successfully carried through 10 steps involving iPSO-SNAr reaction, neutral reduction and acid cyclization. All the steps in this synthetic sequence were assisted by microwave (MW) irradiation. The polymer support was cleaved to release the final head to tail bisbenzimidazoles in an efficient process. (c) 2006 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleParallel synthesis of amino bis-benzimidazoles by multistep microwave irradiationen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.tetlet.2006.02.015en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.citation.volume47en_US
dc.citation.issue15en_US
dc.citation.spage2601en_US
dc.citation.epage2604en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000236438100031-
dc.citation.woscount17-
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