完整後設資料紀錄
DC 欄位語言
dc.contributor.authorWu, HJen_US
dc.contributor.authorChern, JHen_US
dc.date.accessioned2014-12-08T15:01:14Z-
dc.date.available2014-12-08T15:01:14Z-
dc.date.issued1997-12-29en_US
dc.identifier.issn0040-4020en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0040-4020(97)10228-9en_US
dc.identifier.urihttp://hdl.handle.net/11536/136-
dc.description.abstractThe synthesis of 4-oxo- and 4-anti-formyl-8,10,12,13-tetraoxapentacyclo[5.5.1.0(2,6).0(3,11).0(5,9)]tridecanes has been accomplished. Ozonolysis of compounds 10a,b and 12a-c in dichloromethane at -78 degrees C followed by reduction with dimethyl sulfide gave the title compounds, 4-oxo-tetraoxa-cages 11a,b and 14a-c, in moderate yields. Ozonolysis of the endo-syn isomers 15a,b and 18a,b under the same reaction conditions gave 4-anti-formyl-tetraoxa-cages 17a,b and 20a,b, respectively. (C) 1997 Published by Elsevier Science Ltd.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of 4-oxo- and 4-anti-formyl-8,10,12,13-tetraoxapentacyclo[5.5.1.0(2,6).0(3,11).0(5,9)]tridecanesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0040-4020(97)10228-9en_US
dc.identifier.journalTETRAHEDRONen_US
dc.citation.volume53en_US
dc.citation.issue52en_US
dc.citation.spage17653en_US
dc.citation.epage17668en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.contributor.departmentDepartment of Applied Chemistryen_US
顯示於類別:期刊論文


文件中的檔案:

  1. A1997YK20800007.pdf

若為 zip 檔案,請下載檔案解壓縮後,用瀏覽器開啟資料夾中的 index.html 瀏覽全文。