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dc.creatorSaičić, Radomir
dc.creatorČeković, Ž.
dc.date.accessioned2018-11-22T00:01:30Z
dc.date.available2018-11-22T00:01:30Z
dc.date.issued1997
dc.identifier.issn0352-5139
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/59
dc.description.abstractIn this paper an efficient synthetic approach to bridged cyclooctanone framework is described, which is based on cyclization/alkoxy radical fragmentation as a tactical combination of reactions. While the hypoiodite reaction of alcohol 11 proceeds in a normal fashion, the hypobromite reaction of the same precursor unexpectedly affords dibromo derivative 14, which, in turn, shows unusual reactivity in the presence of cesium acetate.en
dc.rightsrestrictedAccess
dc.sourceJournal of the Serbian Chemical Society
dc.subjectAldol reactionen
dc.subjectCyclooctaneen
dc.subjectFragmentationen
dc.subjectRadicalsen
dc.subjectTaxaneen
dc.titleCyclization/alkoxy radical fragmentation tandem: An efficient approach to the synthesis of bridged cyclooctane derivativesen
dc.typearticle
dc.rights.licenseBY-NC-ND
dc.citation.volume62
dc.citation.issue9
dc.citation.spage727
dc.citation.epage735
dc.citation.other62(9): 727-735
dc.identifier.scopus2-s2.0-0040090211
dc.identifier.rcubKon_1097


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