Intramolecular Diels-Alder reaction of 2-diphenylphosphinyl-5-(propargyloxymethyl)furans followed by nucleophilic 1,2-rearrangement of the phosphinyl group
| dc.citation.epage | 6194 | en_US |
| dc.citation.issue | 35 | en_US |
| dc.citation.spage | 6192 | en_US |
| dc.citation.volume | 48 | en_US |
| dc.citation.woscount | 5 | |
| 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.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | 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.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.identifier.doi | 10.1016/j.tetlet.2007.06.163 | en_US |
| dc.identifier.issn | 0040-4039 | en_US |
| dc.identifier.journal | TETRAHEDRON LETTERS | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/j.tetlet.2007.06.163 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/10418 | |
| dc.identifier.wosnumber | WOS:000248985800030 | |
| 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 |