dc.contributor.author | Bajaj, Kiran | |
dc.date.accessioned | 2021-11-11T11:23:24Z | |
dc.date.available | 2021-11-11T11:23:24Z | |
dc.date.issued | 2013-01-16 | |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/10.1002/psc.2483 | |
dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3502 | |
dc.description.abstract | Nα-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.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Chemistry | en_US |
dc.subject | Benzotriazolide | en_US |
dc.subject | Histidine | en_US |
dc.title | Introduction of histidine units using benzotriazolide activation | en_US |
dc.type | Article | en_US |
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