Threonine-proline-chimeras, a valuable building block for peptidomimetic design: A review

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dc.contributor.authorMollica, A.
dc.contributor.authorZengin, Gökhan
dc.date.accessioned2020-03-26T19:32:06Z
dc.date.available2020-03-26T19:32:06Z
dc.date.issued2016
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractThreonine-proline chimeras are not so abundant in nature as the other proine-chimeras and their functionalization is also restricted to the third position on the pyrrolidine ring. Despite these aspects the synthetic procedures adopted to obtain these products are straightforward and well-described in literature, as reported in the following review. © 2016 Bentham Science Publishers.en_US
dc.identifier.doi10.2174/1573407212666160511162638en_US
dc.identifier.endpage228en_US
dc.identifier.issn1573-4072en_US
dc.identifier.issue3en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage221en_US
dc.identifier.urihttps://dx.doi.org/10.2174/1573407212666160511162638
dc.identifier.urihttps://hdl.handle.net/20.500.12395/34327
dc.identifier.volume12en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherBentham Science Publishers B.V.en_US
dc.relation.ispartofCurrent Bioactive Compoundsen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectDeckmann reactionen_US
dc.subjectDiastereoselective cyclizationen_US
dc.subjectMichael condensationen_US
dc.subjectSharpless epoxidationen_US
dc.subjectThreonine-proline chimerasen_US
dc.titleThreonine-proline-chimeras, a valuable building block for peptidomimetic design: A reviewen_US
dc.typeReviewen_US

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