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 Field | Value | Language |
---|---|---|
dc.contributor.author | Pehere, A.D. | - |
dc.contributor.author | Zhang, X. | - |
dc.contributor.author | Abell, A.D. | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Australian Journal of Chemistry: an international journal for chemical science, 2017; 70(2):138-151 | - |
dc.identifier.issn | 0004-9425 | - |
dc.identifier.issn | 1445-0038 | - |
dc.identifier.uri | http://hdl.handle.net/2440/117226 | - |
dc.description.abstract | Macrocycles 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.statementofresponsibility | Ashok D. Pehere, Xiaozhou Zhang, and Andrew D. Abell | - |
dc.language.iso | en | - |
dc.publisher | CSIRO Publishing | - |
dc.rights | © CSIRO 2017 | - |
dc.source.uri | http://dx.doi.org/10.1071/ch16532 | - |
dc.title | Macrocyclic peptidomimetics prepared by ring-closing metathesis and azide-alkyne cycloaddition | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1071/CH16532 | - |
pubs.publication-status | Published | - |
dc.identifier.orcid | Abell, A.D. [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.