Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/8998
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorKung, KKY-
dc.creatorWong, KF-
dc.creatorLeung, KC-
dc.creatorWong, MK-
dc.date.accessioned2015-06-23T09:16:15Z-
dc.date.available2015-06-23T09:16:15Z-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10397/8998-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleN-terminal α-amino group modification of peptides by an oxime formation-exchange reaction sequenceen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage6888-
dc.identifier.epage6890-
dc.identifier.volume49-
dc.identifier.issue61-
dc.identifier.doi10.1039/c3cc42261e-
dcterms.abstractA site-specific and efficient method for N-terminal modification of peptides using oxone for selective oxidation of N-terminal α-amino groups of peptides to oximes followed by transoximation with O-substituted hydroxylamines has been developed.-
dcterms.bibliographicCitationChemical communications, 2013, v. 49, no. 61, p. 6888-6890-
dcterms.isPartOfChemical communications-
dcterms.issued2013-
dc.identifier.isiWOS:000321384200021-
dc.identifier.scopus2-s2.0-84879918541-
dc.identifier.eissn1364-548X-
dc.identifier.rosgroupidr62554-
dc.description.ros2012-2013 > Academic research: refereed > Publication in refereed journal-
Appears in Collections:Journal/Magazine Article
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