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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3502
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dc.contributor.authorBajaj, Kiran-
dc.date.accessioned2021-11-11T11:23:24Z-
dc.date.available2021-11-11T11:23:24Z-
dc.date.issued2013-01-16-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/psc.2483-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3502-
dc.description.abstractNα-Boc-Nim-(4-toluenesulfonyl-l-histidylbenzotriazole) enables convenient acylation of N-, O-, S-, and C-nucleophiles with no detectable racemization. We report efficient syntheses of novel histidine-containing di-, tri-, and tetra-peptides and models for the preparation of potentially biologically active histidine N-, O-, S-, and C-conjugates. Copyright © 2013 European Peptide Society and John Wiley & Sons, Ltd.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectBenzotriazolideen_US
dc.subjectHistidineen_US
dc.titleIntroduction of histidine units using benzotriazolide activationen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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