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dc.contributor.authorLin, HCen_US
dc.contributor.authorWu, HJen_US
dc.date.accessioned2014-12-08T15:45:47Z-
dc.date.available2014-12-08T15:45:47Z-
dc.date.issued2000-01-14en_US
dc.identifier.issn0040-4020en_US
dc.identifier.urihttp://hdl.handle.net/11536/30806-
dc.description.abstractA new entry for the synthesis of diacetal trioxa-cage compounds via oxirane-induced sequential cyclization reaction of 2,3-bis-endo-diacylbicyclo[2.2.1]-5-heptenes and 2,3-bis-endo-diacylbicyclo[2.2.2]-5-octenes is reported. In the case of bicyclo[2.2.2]octenes, sequential cyclization reaction induced by iodine as electrophile failed. We have also demonstrated that dimethyldioxirane can selectively oxidize hemiacetals to give lactones with the secondary hydroxy group intact. (C) 2000 Elsevier Science Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectdimethyldioxiraneen_US
dc.subjectdiacetal trioxa-cage compoundsen_US
dc.subjectlactonesen_US
dc.titleSynthesis of diacetal trioxa-cage compounds via reaction of bicycle [2.2.1]heptenes and bicyclo[2.2.2]octenes with dimethyldioxiraneen_US
dc.typeArticleen_US
dc.identifier.journalTETRAHEDRONen_US
dc.citation.volume56en_US
dc.citation.issue3en_US
dc.citation.spage341en_US
dc.citation.epage350en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000084896900001-
dc.citation.woscount10-
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