Intramolecular Diels-Alder reaction of 2-diphenylphosphinyl-5-(propargyloxymethyl)furans followed by nucleophilic 1,2-rearrangement of the phosphinyl group

doi:10.1016/j.tetlet.2007.06.163

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Wu, Hsien-Jen	en_US
dc.contributor.author	Liu, Chuan-Fang	en_US
dc.contributor.author	Wang, Zhongyi	en_US
dc.contributor.author	Lin, Hui-Chang	en_US
dc.date.accessioned	2014-12-08T15:13:29Z	-
dc.date.available	2014-12-08T15:13:29Z	-
dc.date.issued	2007-08-27	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2007.06.163	en_US
dc.identifier.uri	http://hdl.handle.net/11536/10418	-
dc.description.abstract	The base-catalyzed intramolecular Diels-Alder reactions of 2-diphenylphosphinyl-5-(propargyloxymethyl)furans 2a-e gave the tetrahydrofuran ring annulated o-diphenylphosphinophenols 3a-e in 70-80% yields, a novel reaction involving an intramolecular Diels-Alder reaction of furan diene with allenyl ether dienophile followed by a nucleophilic 1,2-rearrangement of the diphenylphosphinyl group. (C) 2007 Elsevier Ltd. All rights reserved.	en_US
dc.language.iso	en_US	en_US
dc.title	Intramolecular Diels-Alder reaction of 2-diphenylphosphinyl-5-(propargyloxymethyl)furans followed by nucleophilic 1,2-rearrangement of the phosphinyl group	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/j.tetlet.2007.06.163	en_US
dc.identifier.journal	TETRAHEDRON LETTERS	en_US
dc.citation.volume	48	en_US
dc.citation.issue	35	en_US
dc.citation.spage	6192	en_US
dc.citation.epage	6194	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:000248985800030	-
dc.citation.woscount	5	-
顯示於類別：	期刊論文

文件中的檔案：

000248985800030.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。