A novel photoinduced ring opening and isomerization of adamantane-2-spiro isoxazolines using MO(CO)(6)
| dc.citation.epage | 7183 | en_US |
| dc.citation.issue | 40 | en_US |
| dc.citation.spage | 7179 | en_US |
| dc.citation.volume | 47 | en_US |
| dc.citation.woscount | 9 | |
| dc.contributor.author | Senthilvelan, Annamalai | en_US |
| dc.contributor.author | Lee, Gene-Hsiang | en_US |
| dc.contributor.author | Chung, Wen-Sheng | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:15:38Z | |
| dc.date.available | 2014-12-08T15:15:38Z | |
| dc.date.issued | 2006-10-02 | en_US |
| dc.description.abstract | The MO(Co)(6)-mediated photoinduced ring-opening reactions of adamantane isoxazolines involve novel rearrangement that provide enaminoketones as major products and beta-hydroxy ketones as minor ones; in contrast, only beta-hydroxy ketones and alpha,beta-unsaturated ketones were obtained under thermal condition. (c) 2006 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.doi | 10.1016/j.tetlet.2006.07.156 | 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.2006.07.156 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/11687 | |
| dc.identifier.wosnumber | WOS:000240887000013 | |
| dc.language.iso | en_US | en_US |
| dc.subject | adamantane isoxazolines | en_US |
| dc.subject | photorearrangement | en_US |
| dc.subject | isomerization | en_US |
| dc.subject | enaminoketones | en_US |
| dc.title | A novel photoinduced ring opening and isomerization of adamantane-2-spiro isoxazolines using MO(CO)(6) | en_US |
| dc.type | Article | en_US |