Synthesis of a Furanosyl-pyranone Derivative Related to the Tri-O-heterocyclic Core of Herbicidins
| dc.citation.epage | 425 | en_US |
| dc.citation.issue | 3 | en_US |
| dc.citation.spage | 421 | en_US |
| dc.citation.volume | 59 | en_US |
| dc.citation.woscount | 0 | |
| dc.contributor.author | Hsu, Ching-Yun | en_US |
| dc.contributor.author | Lee, I-Chi | en_US |
| dc.contributor.author | Lico, Larry S. | en_US |
| dc.contributor.author | Uang, Biing-Jiun | en_US |
| dc.contributor.author | Hung, Shang-Cheng | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:21:53Z | |
| dc.date.available | 2014-12-08T15:21:53Z | |
| dc.date.issued | 2012-03-01 | en_US |
| dc.description.abstract | A new compound that is structurally related to the undecose ring structure of herbicidins has been prepared. The synthesis of this novel furanosyl-pyranone derivative was made possible through the regioselective reductive ring-opening of a 3,5-O-benzylidene-D-xylofuranose and the hetero-Diels-Alder reaction of an aldehyde and a Danishefsky-type diene. The highly functionalized pyranone derivative can be a useful precursor for the synthesis of herbicidins. | en_US |
| dc.identifier.doi | 10.1002/jccs.201100744 | en_US |
| dc.identifier.issn | 0009-4536 | en_US |
| dc.identifier.journal | JOURNAL OF THE CHINESE CHEMICAL SOCIETY | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1002/jccs.201100744 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/15577 | |
| dc.identifier.wosnumber | WOS:000301092800023 | |
| dc.language.iso | en_US | en_US |
| dc.subject | Benzylidene acetal | en_US |
| dc.subject | Cycloaddition | en_US |
| dc.subject | Danishefsky-type diene | en_US |
| dc.subject | Herbicidins | en_US |
| dc.subject | Regioselectivity | en_US |
| dc.title | Synthesis of a Furanosyl-pyranone Derivative Related to the Tri-O-heterocyclic Core of Herbicidins | en_US |
| dc.type | Article | en_US |