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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/34849
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dc.contributor.authorGardiner, J.-
dc.contributor.authorAnderson, K.-
dc.contributor.authorDownard, A.-
dc.contributor.authorAbell, A.-
dc.date.issued2004-
dc.identifier.citationJournal of Organic Chemistry, 2004; 69(10):3375-3382-
dc.identifier.issn0022-3263-
dc.identifier.issn1520-6904-
dc.identifier.urihttp://hdl.handle.net/2440/34849-
dc.descriptionCopyright © 2004 American Chemical Society-
dc.description.abstractHere we report a versatile ring-closing metathesis-based approach to 5-, 6-, and 7-membered cyclic β-amino esters starting with simple and readily available building blocks - methionine, allylglycine, and serine - where the nature of the amino acid determines the size of the carbocyclic ring.-
dc.description.statementofresponsibilityJames Gardiner, Kelly H. Anderson, Alison Downard, and Andrew D. Abell-
dc.language.isoen-
dc.publisherAmer Chemical Soc-
dc.source.urihttp://dx.doi.org/10.1021/jo049794g-
dc.subjectEsters-
dc.subjectAllylglycine-
dc.subjectAmino Acids-
dc.subjectMethionine-
dc.subjectSerine-
dc.subjectMolecular Structure-
dc.subjectCyclization-
dc.subjectCatalysis-
dc.titleThe synthesis of cyclic β-amino acid esters from Methionone, Allylglycine, and Serine-
dc.title.alternativeThe synthesis of cyclic beta-amino acid esters from Methionone, Allylglycine, and Serine-
dc.typeJournal article-
dc.identifier.doi10.1021/jo049794g-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]-
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Chemistry publications

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