Regioselective Piperidine-Catalyzed Tandem Imination-Isocyanate Annulation to Fused Tricyclic Triazines

doi:10.1021/co400159z

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Barve, Indrajeet J.	en_US
dc.contributor.author	Chen, Chih-Hau	en_US
dc.contributor.author	Kao, Chih-Hsien	en_US
dc.contributor.author	Sun, Chung-Ming	en_US
dc.date.accessioned	2014-12-08T15:36:06Z	-
dc.date.available	2014-12-08T15:36:06Z	-
dc.date.issued	2014-05-01	en_US
dc.identifier.issn	2156-8952	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/co400159z	en_US
dc.identifier.uri	http://hdl.handle.net/11536/24454	-
dc.description.abstract	A novel tandem imination-isocyanate-mediated annulation was explored. Ionic liquid-immobilized 2-aminobenzimidazoles react sequentially with aldehydes and isocyanates to give highly functionalized benzimidazole-embedded triazines. The second-stage transformation revealed that the formation of triazinone functionality is entirely regioselective to allow rapid assembly of biologically interesting tricyclic skeletons. In conjunction with the application of microwave irradiation and IL support, this method provides an efficient route to access substituted benzoimidazotriazines.	en_US
dc.language.iso	en_US	en_US
dc.subject	tandem reaction	en_US
dc.subject	imination	en_US
dc.subject	isocyanate-mediated annulation	en_US
dc.subject	benzoimidazotriazine	en_US
dc.subject	ionic liquid	en_US
dc.subject	microwave	en_US
dc.title	Regioselective Piperidine-Catalyzed Tandem Imination-Isocyanate Annulation to Fused Tricyclic Triazines	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1021/co400159z	en_US
dc.identifier.journal	ACS COMBINATORIAL SCIENCE	en_US
dc.citation.volume	16	en_US
dc.citation.issue	5	en_US
dc.citation.spage	244	en_US
dc.citation.epage	249	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:000335940000008	-
dc.citation.woscount	1	-
顯示於類別：	期刊論文

文件中的檔案：

000335940000008.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。