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dc.contributor.authorMalins, Lara R.
dc.contributor.authorPayne, Richard J.
dc.date.accessioned2020-06-19
dc.date.available2020-06-19
dc.date.issued2014-10-03
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S1367593114001306
dc.identifier.urihttps://hdl.handle.net/2123/22607
dc.description.abstractNative chemical ligation continues to play a pivotal role in the synthesis of increasingly complex peptide and protein targets twenty years after its initial report. This opinion article will highlight a number of recent, powerful extensions of the technology that have expanded the scope of the reaction, accelerated ligation rates, enabled chemoselective post-ligation modifications, and streamlined the ligation of multiple peptide fragments. These advances have facilitated the synthesis of a number of impressive protein targets to date and hold great promise for the continued application of native chemical ligation for the detailed study of protein structure and function.en
dc.language.isoen_USen
dc.publisherElsevieren
dc.relationARC FT130100150en
dc.rightsOtheren
dc.titleRecent extensions to native chemical ligation for the chemical synthesis of peptides and proteinsen
dc.typeArticleen
dc.subject.asrcFoR::030599 - Organic Chemistry not elsewhere classifieden
dc.identifier.doi10.1016/j.cbpa.2014.09.021
dc.type.pubtypeAuthor accepted manuscripten
dc.relation.arcFT130100150
usyd.facultySeS faculties schools::Faculty of Scienceen


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