完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Lin, RL | en_US |
dc.contributor.author | Wu, CY | en_US |
dc.contributor.author | Chern, JH | en_US |
dc.contributor.author | Wu, HJ | en_US |
dc.date.accessioned | 2014-12-08T15:02:35Z | - |
dc.date.available | 2014-12-08T15:02:35Z | - |
dc.date.issued | 1996-06-01 | en_US |
dc.identifier.issn | 0009-4536 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/1247 | - |
dc.description.abstract | Tetraacetal tetraoxa-cage compounds 3a, 3b, 4a, 4b, 7, 13, 14, and 15 were synthesized by a short sequence. They were obtained from ozonolysis of endo adducts 1a, 1b, 2a, 2b, and 6 in dichloromethane at -78 degrees C followed by reduction with dimethyl sulfide. Ozonolysis of 7-anti-trimethylsilyl-5,6-bis-endo-diacetylnorbornene 8 under the same reaction conditions did not give the tetraoxa-cage 9. The methylsulfinyl era-cage 13 derived from 1-methylthio-5,6-bis-endo-diacetylnorbornene 11 was converted to com pounds 14 and 15. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Synthesis of tetraacetal tetraoxa-cage compounds with alkyl substituents at different sites of the oxa-cage skeleton | en_US |
dc.type | Article | en_US |
dc.identifier.journal | JOURNAL OF THE CHINESE CHEMICAL SOCIETY | en_US |
dc.citation.volume | 43 | en_US |
dc.citation.issue | 3 | en_US |
dc.citation.spage | 289 | en_US |
dc.citation.epage | 295 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:A1996UV70900012 | - |
dc.citation.woscount | 23 | - |
顯示於類別: | 期刊論文 |