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dc.contributor.authorLai, Jin-Jien_US
dc.contributor.authorSalunke, Deepak B.en_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2014-12-08T15:06:53Z-
dc.date.available2014-12-08T15:06:53Z-
dc.date.issued2010-05-21en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol100436ren_US
dc.identifier.urihttp://hdl.handle.net/11536/5389-
dc.description.abstractSynthesis of amino acid and indoline-substituted dinitrobenzene on a soluble polymer support (PEG) and its further reductive double-ring closure to afford structurally diverse indolo-fused pyrazino-/diazepinoquinoxalinones is described. Traceless synthesis of quinoxalinones coupled with application of the Pictet-Spengler-type condensation reaction furnished these novel scaffolds. These hitherto novel heterocycles are synthesized in shorter times under microwave irradiation conditions in comparison with that of classical reaction conditions.en_US
dc.language.isoen_USen_US
dc.titleMultistep Microwave-Assisted Divergent Synthesis of Indolo-Fused Pyrazino-/Diazepinoquinoxalinones on PEG Supporten_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol100436ren_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume12en_US
dc.citation.issue10en_US
dc.citation.spage2174en_US
dc.citation.epage2177en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000277531000002-
dc.citation.woscount24-
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