Traceless Synthesis of Hydantoin Fused Tetrahydro-beta-carboline on Ionic Liquid Support in Green Media
| dc.citation.epage | 4829 | en_US |
| dc.citation.issue | 21 | en_US |
| dc.citation.spage | 4826 | en_US |
| dc.citation.volume | 11 | en_US |
| dc.citation.woscount | 32 | |
| dc.contributor.author | Maiti, Barnali | en_US |
| dc.contributor.author | Chanda, Kaushik | en_US |
| dc.contributor.author | Sun, Chung-Ming | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | 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.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.identifier.doi | 10.1021/ol901857h | en_US |
| dc.identifier.issn | 1523-7060 | en_US |
| dc.identifier.journal | ORGANIC LETTERS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1021/ol901857h | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/6443 | |
| dc.identifier.wosnumber | WOS:000271097100016 | |
| 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 |