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dc.contributor.authorLin, RLen_US
dc.contributor.authorWu, CYen_US
dc.contributor.authorChern, JHen_US
dc.contributor.authorWu, HJen_US
dc.date.accessioned2014-12-08T15:02:35Z-
dc.date.available2014-12-08T15:02:35Z-
dc.date.issued1996-06-01en_US
dc.identifier.issn0009-4536en_US
dc.identifier.urihttp://hdl.handle.net/11536/1247-
dc.description.abstractTetraacetal 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.isoen_USen_US
dc.titleSynthesis of tetraacetal tetraoxa-cage compounds with alkyl substituents at different sites of the oxa-cage skeletonen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.citation.volume43en_US
dc.citation.issue3en_US
dc.citation.spage289en_US
dc.citation.epage295en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1996UV70900012-
dc.citation.woscount23-
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