Sequential [3+2] and [4+2] Cycloadditions for Stereoselective Synthesis of a Novel Polyheterocyclic Scaffold
| dc.citation.epage | 355 | en_US |
| dc.citation.issue | 7 | en_US |
| dc.citation.spage | 350 | en_US |
| dc.citation.volume | 15 | en_US |
| dc.citation.woscount | 0 | |
| dc.contributor.author | Lu, Qing | en_US |
| dc.contributor.author | Xin Huang | en_US |
| dc.contributor.author | Song, Gonghua | en_US |
| dc.contributor.author | Sun, Chung-Ming | en_US |
| dc.contributor.author | Jasinski, Jerry P. | en_US |
| dc.contributor.author | Keeley, Amanda C. | en_US |
| dc.contributor.author | Zhang, Wei | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:31:12Z | |
| dc.date.available | 2014-12-08T15:31:12Z | |
| dc.date.issued | 2013-07-01 | en_US |
| dc.description.abstract | A strategy of combining [3 + 2] cycloaddition and intramolecular Diels-Alder reaction is developed for the [3 + 2] cycloaddition of azomethine ylides and maleimides were derivatized for intramolecular Diels-Alder reaction of furan to form highly condensed heterocyclic products as racemic single diastereomers. | en_US |
| dc.identifier.doi | 10.1021/co400026s | en_US |
| dc.identifier.issn | 2156-8952 | en_US |
| dc.identifier.journal | ACS COMBINATORIAL SCIENCE | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1021/co400026s | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/22221 | |
| dc.identifier.wosnumber | WOS:000321793500005 | |
| dc.language.iso | en_US | en_US |
| dc.subject | sequential cycloadditions | en_US |
| dc.subject | stereoselective annulation | en_US |
| dc.subject | [3+2] cycloaddition | en_US |
| dc.subject | intramolecular Diels-Alder reaction | en_US |
| dc.subject | polyheterocyclic scaffold | en_US |
| dc.title | Sequential [3+2] and [4+2] Cycloadditions for Stereoselective Synthesis of a Novel Polyheterocyclic Scaffold | en_US |
| dc.type | Article | en_US |