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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/34848
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dc.contributor.authorAbell, A.-
dc.contributor.authorGardiner, J.-
dc.date.issued2002-
dc.identifier.citationOrganic Letters, 2002; 4(21):3663-3666-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttp://hdl.handle.net/2440/34848-
dc.descriptionCopyright © 2002 American Chemical Society-
dc.description.abstract[structure: see text] A versatile ring-closing metathesis (RCM) approach has been developed for the preparation of cis and trans cyclohexenyl-based beta-amino acids that are either unsubstituted (3) or substituted (10 and 12) at the alpha-position.-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.source.urihttp://pubs.acs.org/cgi-bin/abstract.cgi/orlef7/2002/4/i21/abs/ol0266121.html-
dc.subjectCyclohexanes-
dc.subjectAmino Acids-
dc.subjectMolecular Structure-
dc.subjectCyclohexenes-
dc.titleSynthesis of substituted cyclohexenyl-based beta-amino acids by ring-closing metathesis-
dc.typeJournal article-
dc.identifier.doi10.1021/ol0266121-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]-
Appears in Collections:Aurora harvest 6
Chemistry publications

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