Aziridine-Mediated Ligation at Phenylalanine and Tryptophan Sites

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dc.contributor.authorSakhuja, Rajeev
dc.contributor.authorBajaj, Kiran
dc.date.accessioned2021-11-11T10:59:22Z
dc.date.available2021-11-11T10:59:22Z
dc.date.issued2017-05-23
dc.description.abstractAn efficient approach towards peptide synthesis that allows easy access to variety of small peptides via one-pot aziridine-mediated ligation/desulfurization strategy has been described. The protocol afforded a library of phenylalanine- and tryptophan-containing α-peptides in good yields by regioselective ring-opening of aziridine-3-aryl-2-carboxylates with peptide thioacids, followed by desulfurization.en_US
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/asia.201700538
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3358
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectAziridine-Mediateden_US
dc.subjectPhenylalanineen_US
dc.subjectTryptophanen_US
dc.titleAziridine-Mediated Ligation at Phenylalanine and Tryptophan Sitesen_US
dc.typeArticleen_US

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