完整後設資料紀錄
DC 欄位語言
dc.contributor.authorHo, Tse-Loken_US
dc.contributor.authorTang, Binen_US
dc.contributor.authorMa, Guohuaen_US
dc.contributor.authorXu, Pengfeien_US
dc.date.accessioned2014-12-08T15:21:53Z-
dc.date.available2014-12-08T15:21:53Z-
dc.date.issued2012-03-01en_US
dc.identifier.issn0009-4536en_US
dc.identifier.urihttp://dx.doi.org/10.1002/jccs.201100664en_US
dc.identifier.urihttp://hdl.handle.net/11536/15578-
dc.description.abstractSynthesis of (+/-)-diospongin A has been achieved from the (2SR,4RS)-pentane-1,2,4,5-tetraol in six steps. An intermediate has also been converted into yashabushidiol A. This work features a desymmetric cyclization and reduction of a meso-1,7-diarylheptanoid precursor to furnish the desired cis-2,6-disubstituted tetrahydropyran.en_US
dc.language.isoen_USen_US
dc.subject(2SR,4RS)-pentane-1,2,4,5-tetraolen_US
dc.subjectDithiane alkylationen_US
dc.subjectDesulfurizationen_US
dc.subjectmeso-1,7-Diarylheptanoidsen_US
dc.subjectCyclizationen_US
dc.titleConcise Synthesis of Yashabushidiol A and (+/-)-Diospongin Aen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/jccs.201100664en_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.citation.volume59en_US
dc.citation.issue3en_US
dc.citation.spage455en_US
dc.citation.epage458en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000301092800028-
dc.citation.woscount1-
顯示於類別:期刊論文


文件中的檔案:

  1. 000301092800028.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。