Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chang, Chia-Mao | en_US |
dc.contributor.author | Kulkarni, Manohar V. | en_US |
dc.contributor.author | Chen, Chih-Hau | en_US |
dc.contributor.author | Wang, Chi-Hsiang | en_US |
dc.contributor.author | Sun, Chung-Ming | en_US |
dc.date.accessioned | 2014-12-08T15:12:15Z | - |
dc.date.available | 2014-12-08T15:12:15Z | - |
dc.date.issued | 2008-05-01 | en_US |
dc.identifier.issn | 1520-4766 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1021/cc7002045 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/9421 | - |
dc.description.abstract | A well-sustained multistep synthetic protocol has been designed for the PEG-functionalized aromatic acid amide to generate a molecular library of 2-alkylthio bis-benzimidazoles. An attempted synthesis of benzimidazole-2-thiol in dichloromethane has led to S-chloromethyl methyl sulfides, mimicking bacterial enzymatic systems. Regioselective S-alkylation was brought about under controlled conditions using a mild base at room temperature. The polymer-free compounds, 2-sulfanylated bisbenzimidazoles, were obtained in high yields and high purities. Chemical shift changes in proton and carbon NMR-have been employed to monitor the progress of the reaction steps and to prove the site of S-alkylation, respectively. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Parallel synthesis of 2-sulphanylated bis-benzimidazoles on soluble polymer support | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1021/cc7002045 | en_US |
dc.identifier.journal | JOURNAL OF COMBINATORIAL CHEMISTRY | en_US |
dc.citation.volume | 10 | en_US |
dc.citation.issue | 3 | en_US |
dc.citation.spage | 466 | en_US |
dc.citation.epage | 474 | 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:000255848700021 | - |
dc.citation.woscount | 11 | - |
Appears in Collections: | Articles |
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