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Aziridine-Mediated Ligation at Phenylalanine and Tryptophan Sites

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dc.contributor.author Sakhuja, Rajeev
dc.contributor.author Bajaj, Kiran
dc.date.accessioned 2021-11-11T10:59:22Z
dc.date.available 2021-11-11T10:59:22Z
dc.date.issued 2017-05-23
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/asia.201700538
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3358
dc.description.abstract An 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.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Chemistry en_US
dc.subject Aziridine-Mediated en_US
dc.subject Phenylalanine en_US
dc.subject Tryptophan en_US
dc.title Aziridine-Mediated Ligation at Phenylalanine and Tryptophan Sites en_US
dc.type Article en_US


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