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dc.contributor.authorTsai, SHen_US
dc.contributor.authorWu, HJen_US
dc.contributor.authorChung, WSen_US
dc.date.accessioned2014-12-08T15:02:18Z-
dc.date.available2014-12-08T15:02:18Z-
dc.date.issued1996-10-01en_US
dc.identifier.issn0009-4536en_US
dc.identifier.urihttp://hdl.handle.net/11536/988-
dc.description.abstract3,5,7-Trioxapentacyclo[7.2.1.0(2,8).0(4,11).0(6,10)] dodecane, the parent compound of novel diacetal trioxa-cages, was synthesized from maleic anhydride cyclopentadiene adduct 1 by a four-step sequence. Attempts for the synthesis of monoaza dioxa-cage 12 failed. Ozonolysis of compound 9 in CH2Cl2-EtOH (1:1) at -78 degrees C followed by reduction with Me(2)S gave 13 in 65% yield.en_US
dc.language.isoen_USen_US
dc.subjectunsubstituted diacetal trioxa-cageen_US
dc.titleSynthesis of 3,5,7-trioxapentacyclo[7.2.1.0(2,8).0(4,11).0(6,10)]dodecane. A novel diacetal trioxa-cageen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.citation.volume43en_US
dc.citation.issue5en_US
dc.citation.spage445en_US
dc.citation.epage449en_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
dc.identifier.wosnumberWOS:A1996VT72400011-
dc.citation.woscount17-
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