New Dioxa-Cage and Diacetal Trioxa-Cage Compounds
| dc.citation.epage | 1077 | en_US |
| dc.citation.issue | 5 | en_US |
| dc.citation.spage | 1072 | en_US |
| dc.citation.volume | 56 | en_US |
| dc.citation.woscount | 4 | |
| dc.contributor.author | Lin, Hui-Chang | en_US |
| dc.contributor.author | Wu, Hsien-Jen | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:08:39Z | |
| dc.date.available | 2014-12-08T15:08:39Z | |
| dc.date.issued | 2009-10-01 | en_US |
| dc.description.abstract | The synthesis of new dioxa-cage compound 8 and diacetal trioxa-cage compound 17 has been accomplished from dicyclopentadiene in a short sequence. A preliminary study on the pi-facial selectivity of 17, which possesses a new rigid skeleton, is also reported. | en_US |
| dc.identifier.issn | 0009-4536 | en_US |
| dc.identifier.journal | JOURNAL OF THE CHINESE CHEMICAL SOCIETY | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/6638 | |
| dc.identifier.wosnumber | WOS:000272985700028 | |
| dc.language.iso | en_US | en_US |
| dc.subject | Dioxa-Cage | en_US |
| dc.subject | Diacetal trioxa-cage | en_US |
| dc.subject | Facial selectivity | en_US |
| dc.title | New Dioxa-Cage and Diacetal Trioxa-Cage Compounds | en_US |
| dc.type | Article | en_US |
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