完整後設資料紀錄
DC 欄位語言
dc.contributor.authorMaiti, Barnalien_US
dc.contributor.authorChanda, Kaushiken_US
dc.contributor.authorSelvaraju, Manikandanen_US
dc.contributor.authorTseng, Chih-Chungen_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2014-12-08T15:31:25Z-
dc.date.available2014-12-08T15:31:25Z-
dc.date.issued2013-06-01en_US
dc.identifier.issn2156-8952en_US
dc.identifier.urihttp://dx.doi.org/10.1021/co400010yen_US
dc.identifier.urihttp://hdl.handle.net/11536/22329-
dc.description.abstractA novel one-pot, three-component reaction employing variously substituted benzimidazole-linked amino pyridines, aldehydes, and isonitriles catalyzed by scandium(III) triflate under solvent-free conditions were accomplished. This new synthetic methodology facilitates the rapid generation of intricate molecular frameworks in three-dimensional fashion leading to benzinaidazole-imidazo [1,2-a] pyridines. This approach is envisioned as an environmentally benign process and a simple operation to the biological interesting compounds. The present synthetic sequence permits the introduction of three points of structural diversity to expand chemical space with high purity and excellent yields.en_US
dc.language.isoen_USen_US
dc.subjectmicrowave irradiationen_US
dc.subjectbenzimidazole-imidazo[1,2-a]pyridinesen_US
dc.subjectsolvent-freeen_US
dc.subjectbis-heterocyclic skeletonsen_US
dc.subjectthree-component reactionen_US
dc.titleMulticomponent Solvent-Free Synthesis Of Benzimidazolyl Imidazo[1,2-a]-pyridine Under Microwave Irradiationen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/co400010yen_US
dc.identifier.journalACS COMBINATORIAL SCIENCEen_US
dc.citation.volume15en_US
dc.citation.issue6en_US
dc.citation.spage291en_US
dc.citation.epage297en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000320356100004-
dc.citation.woscount15-
顯示於類別:期刊論文


文件中的檔案:

  1. 000320356100004.pdf

若為 zip 檔案,請下載檔案解壓縮後,用瀏覽器開啟資料夾中的 index.html 瀏覽全文。