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The first exclusive regioselective fragmentation of primary ozonides controlled by remote carbonyl groups

dc.citation.epage9356en_US
dc.citation.issue51en_US
dc.citation.spage9353en_US
dc.citation.volume36en_US
dc.citation.woscount27
dc.contributor.authorLin, CCen_US
dc.contributor.authorWu, HJen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:03:00Z
dc.date.available2014-12-08T15:03:00Z
dc.date.issued1995-12-18en_US
dc.description.abstractOzonolysis of compounds 1a-1d in CDCl3 at -78 degrees C regioselectively and stereoselectively gave the corresponding final ozonides 2a-2d as the sole product, which, after treatment with triethylamine, gave the novel convex tetraquinane era-cages 9a-9d in high yields respectively.en_US
dc.identifier.doi10.1016/0040-4039(95)02026-Len_US
dc.identifier.issn0040-4039en_US
dc.identifier.journalTETRAHEDRON LETTERSen_US
dc.identifier.urihttp://dx.doi.org/10.1016/0040-4039(95)02026-Len_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/1594
dc.identifier.wosnumberWOS:A1995TL06800029
dc.language.isoen_USen_US
dc.titleThe first exclusive regioselective fragmentation of primary ozonides controlled by remote carbonyl groupsen_US
dc.typeArticleen_US

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