Multistep Microwave-Assisted Divergent Synthesis of Indolo-Fused Pyrazino-/Diazepinoquinoxalinones on PEG Support

doi:10.1021/ol100436r

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DC Field	Value	Language
dc.contributor.author	Lai, Jin-Ji	en_US
dc.contributor.author	Salunke, Deepak B.	en_US
dc.contributor.author	Sun, Chung-Ming	en_US
dc.date.accessioned	2014-12-08T15:06:53Z	-
dc.date.available	2014-12-08T15:06:53Z	-
dc.date.issued	2010-05-21	en_US
dc.identifier.issn	1523-7060	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/ol100436r	en_US
dc.identifier.uri	http://hdl.handle.net/11536/5389	-
dc.description.abstract	Synthesis 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.iso	en_US	en_US
dc.title	Multistep Microwave-Assisted Divergent Synthesis of Indolo-Fused Pyrazino-/Diazepinoquinoxalinones on PEG Support	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1021/ol100436r	en_US
dc.identifier.journal	ORGANIC LETTERS	en_US
dc.citation.volume	12	en_US
dc.citation.issue	10	en_US
dc.citation.spage	2174	en_US
dc.citation.epage	2177	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000277531000002	-
dc.citation.woscount	24	-
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