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dc.contributor.authorWu, HJen_US
dc.contributor.authorChern, JHen_US
dc.contributor.authorWu, CYen_US
dc.date.accessioned2014-12-08T15:02:00Z-
dc.date.available2014-12-08T15:02:00Z-
dc.date.issued1997-02-17en_US
dc.identifier.issn0040-4020en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0040-4020(96)01188-Xen_US
dc.identifier.urihttp://hdl.handle.net/11536/721-
dc.description.abstractA new route for the synthesis of the title compounds 4a, 4b, 10a, and 10b has been developed via ozonolysis of 2-endo-7-anti-diacylnorbornenes 3a, 3b, 9a, and 9b. The synthesis of the unsubstituted (parent) compound 4a of tetraacetal tetraoxa-cages has been accomplished for the first time by this new entry. Ozonolysis reactions of 3a, 3b, and 9a were also performed in CDCl3 for understanding the final ozonide structures and the ozonation chemistry. Ozonolysis of 3a, 3b, and 9a in CH2Cl2 at -78 degrees C followed by treatment with triethylamine provided an indirect support for the structures of the final ozonides 11a, 11b, and 14. (C) 1997, Elsevier Science Ltd.en_US
dc.language.isoen_USen_US
dc.titleOzonolysis of 2-endo-7-anti-diacylnorbornenes. A new entry for the synthesis of 2,4,6,13-tetraoxapentacyclo[5.5.1.0(3,11).0(5,9).0(8,12)]tridecanesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0040-4020(96)01188-Xen_US
dc.identifier.journalTETRAHEDRONen_US
dc.citation.volume53en_US
dc.citation.issue7en_US
dc.citation.spage2401en_US
dc.citation.epage2414en_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:A1997WJ21100007-
dc.citation.woscount20-
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