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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/4389
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dc.contributor.authorCooper, M.-
dc.contributor.authorWard, A.-
dc.date.issued1997-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 1997; 50(3):181-187-
dc.identifier.issn0004-9425-
dc.identifier.urihttp://hdl.handle.net/2440/4389-
dc.description.abstract<jats:p> Alkyl phenyl selenides derived from the benzeneselenenyl chloride induced cyclization of N-protected pent-4-enylamines can be converted in good yield into the corresponding 2-hydroxymethyl- or 2- alkoxymethyl-substituted pyrrolidines by oxidation to the corresponding selenone, followed by reaction with water (or hydroxide) or with the corresponding alcohol. Details of the reactions and possible mechanisms for the substitution are discussed.</jats:p>-
dc.language.isoen-
dc.publisherCSIRO Publishing-
dc.source.urihttp://dx.doi.org/10.1071/c96148-
dc.titleSynthesis and substitution reactions of N-protected 2-(phenylselenonylmethyl) pyrrolidines-
dc.typeJournal article-
dc.identifier.doi10.1071/C96148-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 2
Chemistry publications

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