Traceless Synthesis of Hydantoin Fused Tetrahydro-beta-carboline on Ionic Liquid Support in Green Media

doi:10.1021/ol901857h

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Maiti, Barnali	en_US
dc.contributor.author	Chanda, Kaushik	en_US
dc.contributor.author	Sun, Chung-Ming	en_US
dc.date.accessioned	2014-12-08T15:08:17Z	-
dc.date.available	2014-12-08T15:08:17Z	-
dc.date.issued	2009-11-05	en_US
dc.identifier.issn	1523-7060	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/ol901857h	en_US
dc.identifier.uri	http://hdl.handle.net/11536/6443	-
dc.description.abstract	A novel ionic liquid (IL) supported, green synthetic protocol has been developed toward the synthesis of oxo and thio hydantoin analogues tethered with tetrahydro-beta-carboline by the use of focused microwave irradiation. IL-bound tryptophan underwent a Pictet-Spengler reaction with various carbonyl compounds to generate the IL-immobilized tetrahydro-beta-carbolines in aqueous isopropanol media. Subsequent reaction of substituted tetra hydro-beta-carboline derivatives with various isocyanates and isothiocyanate provided a three-dimensional combinatorial library in a traceless fashion.	en_US
dc.language.iso	en_US	en_US
dc.title	Traceless Synthesis of Hydantoin Fused Tetrahydro-beta-carboline on Ionic Liquid Support in Green Media	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1021/ol901857h	en_US
dc.identifier.journal	ORGANIC LETTERS	en_US
dc.citation.volume	11	en_US
dc.citation.issue	21	en_US
dc.citation.spage	4826	en_US
dc.citation.epage	4829	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:000271097100016	-
dc.citation.woscount	32	-
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