Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/117226
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPehere, A.-
dc.contributor.authorZhang, X.-
dc.contributor.authorAbell, A.-
dc.date.issued2017-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 2017; 70(2):138-151-
dc.identifier.issn0004-9425-
dc.identifier.issn1445-0038-
dc.identifier.urihttp://hdl.handle.net/2440/117226-
dc.description.abstractMacrocycles are finding increasing use as a means to define the backbone geometries of peptides and peptidomimetics. Ring-closing metathesis and CuI-catalyzed azide–alkyne cycloaddition are particularly useful for introducing such rings and they do so in high yield and with a good functional group tolerance and compatibility. Here, we present an overview of the use of these two methods, with reference to selected examples and particular reference to b-strand peptidomimetics for use as protease inhibitors.-
dc.description.statementofresponsibilityAshok D. Pehere, Xiaozhou Zhang, and Andrew D. Abell-
dc.language.isoen-
dc.publisherCSIRO Publishing-
dc.rights© CSIRO 2017-
dc.titleMacrocyclic peptidomimetics prepared by ring-closing metathesis and azide-alkyne cycloaddition-
dc.typeJournal article-
dc.identifier.doi10.1071/CH16532-
pubs.publication-statusPublished-
dc.identifier.orcidAbell, A. [0000-0002-0604-2629]-
Appears in Collections:Aurora harvest 3
IPAS publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.